- Open Access
Physiological characteristics of the extreme thermophile Caldicellulosiruptor saccharolyticus: an efficient hydrogen cell factory
© Willquist et al; licensee BioMed Central Ltd. 2010
- Received: 31 August 2010
- Accepted: 22 November 2010
- Published: 22 November 2010
Global concerns about climate changes and their association with the use of fossil fuels have accelerated research on biological fuel production. Biological hydrogen production from hemicellulose-containing waste is considered one of the promising avenues. A major economical issue for such a process, however, is the low substrate conversion efficiency. Interestingly, the extreme thermophilic bacterium Caldicellulosiruptor saccharolyticus can produce hydrogen from carbohydrate-rich substrates at yields close to the theoretical maximum of the dark fermentation process (i.e., 4 mol H2/mol hexose). The organism is able to ferment an array of mono-, di- and polysaccharides, and is relatively tolerant to high partial hydrogen pressures, making it a promising candidate for exploitation in a biohydrogen process. The behaviour of this Gram-positive bacterium bears all hallmarks of being adapted to an environment sparse in free sugars, which is further reflected in its low volumetric hydrogen productivity and low osmotolerance. These two properties need to be improved by at least a factor of 10 and 5, respectively, for a cost-effective industrial process. In this review, the physiological characteristics of C. saccharolyticus are analyzed in view of the requirements for an efficient hydrogen cell factory. A special emphasis is put on the tight regulation of hydrogen production in C. saccharolyticus by both redox and energy metabolism. Suggestions for strategies to overcome the current challenges facing the potential use of the organism in hydrogen production are also discussed.
- Dark Fermentation
- Caldicellulosiruptor Saccharolyticus
- Dark Fermentation Process
Anthropogenic CO2 emissions have generally been recognized as the major contributor to global warming and associated climate changes. Therefore, several measures are being taken to decrease the CO2 emission. In recent years, much effort has been devoted to rendering biofuel production economically competitive to that of fossil fuels, since this will contribute significantly to the reduction of energy-linked environmental impacts. In this quest, the choice of the raw material is of central concern. First-generation biofuels are produced from sucrose and starch-rich substrates, which may compete with human consumption - inevitably driving up market prices. As a remedy, more focus should be directed to second-generation biofuels, produced from non-edible lignocellulosic materials, the most naturally abundant raw material , as well as domestic and industrial wastes. The accompanying significant cost reductions should make biofuels more competitive.
Biohydrogen is a typical example of an environmentally friendly biofuel, with no CO2 emission resulting from its combustion. It can be produced from both lignocellulosic and waste materials [2–5], through biological conversion processes, such as dark fermentation and photofermentation. In the latter, biohydrogen can be produced using purple sulphur or non-sulphur bacteria that convert organic acids to H2 in photon-driven reactions [6, 7]. Although a combination of these two processes is an interesting approach for maximum conversion of the energy contained in carbohydrate-rich substrates into H2, only dark fermentative H2 production is covered in this review.
In total, 12 H2 molecules can be obtained per mole of glucose, based on the overall number of electrons that can be generated in the complete oxidation of the latter. However, dark fermentation is limited to a maximum H2-production efficiency of 33%, i.e., maximally four molecules of H2 can be acquired per molecule of glucose with acetate and CO2 as the other fermentation end products . Yet, this is only possible when the H2 partial pressure (PH2) is kept adequately low , e.g. by continuous stripping of the produced H2 with an inert gas. However, for a cost-effective dark fermentation process it is vital to obtain significantly high H2 yields at relatively elevated PH2, due to the high impact of central costs of feedstock and gas upgrading . Generally, mesophilic (co-)cultures reach H2 yields of ≤ 2 moles/mol hexose , thus exemplifying conversion efficiencies of merely 17%. In addition, these yields are obtained at low PH2 only . On the other hand, based on thermodynamic aspects, thermophilic bacteria and archaea may produce up to the theoretical maximum of 4 mol H2/mol hexose . In general, the low H2 yields obtained in practice by different organisms, in addition to the requirement for low PH2, are major obstacles that need to be overcome before biohydrogen production can be industrially feasible .
Caldicellulosiruptor saccharolyticus is an extreme thermophilic bacterium that can produce high H2 yields [14, 15], and at the same time is relatively insensitive to high PH2. This organism has recently gained increased interest due to its ability to produce thermostable cellulolytic and xylanolytic enzymes [17–21], to grow on complex lignocellulosic carbon sources [2, 22, 23], and to co-metabolize a wide spectrum of monosaccharides including both pentose and hexose sugars . Although C. saccharolyticus possesses these desirable traits and several research articles have been recently published on this heterotrophic strict anaerobe, it has not yet been the subject of a review article. Herein, the physiological properties of C. saccharolyticus will be analyzed to unravel the characteristics required for a superior H2 cell factory. To further underline current insights in this topic, the physiology of C. saccharolyticus will be compared with that of other H2-producing microorganisms.
C. saccharolyticus is a strictly anaerobic, extreme-thermophilic, Gram-positive bacterium that belongs to the Clostridia class. There are to date 13 characterized species in the genus Caldicellulosiruptor, of which C. saccharolyticus is described best, including its whole-genome sequence . C. bescii, formerly known as Anaerocellum thermophilum, is the other species in the genus with its genome also fully sequenced [26, 27]. C. saccharolyticus was isolated from a piece of wood in a hot spring in the Rotorua-Taupo thermal area in New Zealand, of which the waters have neutral pH, and are low in sulphate, salt content and free sugars . Instead, The majority of the sugars present in this environment, such as glucose and xylose, are contained in complex (hemi)cellulosic polymers, which are difficult to access.
C. saccharolyticus is well adapted to the selective pressure of this habitat through the production of various hydrolyzing enzymes, possession of a wide range of high-affinity transport systems, and absence of glucose-based catabolite repression [24, 25, 29], which are all attractive properties for using the organism for industrial purposes. However, being sensitive to high osmotic pressures [30, 31] is one of the undesirable consequences of adaptation to such environment. Interestingly, C. saccharolyticus is non-motile and non-sporulating , although it possesses a complete set of genes for flagella biosynthesis and several genes required for sporulation , signifying a historical genetic record of characteristics that could have been required in past habitats.
The genome of C. saccharolyticus has been sequenced and a microarray-based protocol for genome-wide transcriptome analysis has been developed, which is a major convenience for studying and understanding its physiology . C. saccharolyticus has a relatively small genome of 2,970 kb and 2,760 protein-coding open reading frames (ORFs). From the genome-curation project, several new insights were gained such as the unusually high number of transposons and transposable derivatives C. saccharolyticus possesses, as compared with other organisms . Since transposition increases the chance of genetic alterations, a large number of transposons can enhance the adaptability of this organism and may widen the spectrum of environmental conditions it can grow in, which is beneficial from an industrial point of view. On the other hand, this may also have negative repercussions since it can jeopardize stable fermentation processes. How to balance both impacts in practice needs to be further investigated.
A general favourable property of members of the Clostridia class is their ability to degrade complex polymers such as cellulosic and lignocellulosic materials . Based on growth analysis, C. saccharolyticus can metabolize various carbon sources ranging from monomers, such as xylose, arabinose, glucose, fructose and galactose to α- and β-linked di- and polysaccharides, such as maltose, lactose, sucrose, starch, pullulan, threhalose, xylan and cellulose . C. saccharolyticus can also grow and produce H2 from complex lignocellulosic materials, both pre-treated, such as Miscanthus hydrolysate , sugar beet juice  and paper sludge , and untreated, such as wheat straw , pine wood  and bagasse . The fermentation of these raw materials by C. saccharolyticus has yielded H2, CO2 and acetate as the main metabolic end products [2, 23, 34, 35], with a maximum H2 yield per consumed hexose of 3.0-3.8 mol/mol [2, 34, 35]. Interestingly, cultivations on Miscanthus hydrolysate were accompanied by complete depletion of oligosaccharides and simultaneous oligosaccharide and monosaccharide consumption . C. saccharolyticus degrades complex polymers by producing several cellulolytic and xylanolytic enzymes . Properties of the cellulase and hemicellulase enzymes of this organism as well as their gene structures have been extensively studied . In contrast to cellulolytic clostridia , C. saccharolyticus does not contain a cellulosome complex. C. saccharolyticus is unusual with respect to its possession of a multifunctional, multi-domain organisation for the majority of its β-glucanases . The majority of the xylanases in C. saccharolyticus are clustered in a large gene cluster, and another cluster of genes involved in xylose metabolism is in close proximity . Detailed information on glycoside hydrolases and other carbohydrate active enzymes encoded by C. saccharolyticus genome can be retrieved from the Carbohydrate Active Enzymes database (CAZy; http://www.cazy.org/; ).
The manual curation of the genome sequence of C. saccharolyticus indicated that it possesses an unusually high number of ATP-binding cassette (ABC) transporter genes (i.e., at least 177 ABC transporter genes) ; many of which are responsible for the transport of monomeric and dimeric sugars. C. saccharolyticus has only one sugar phosphotransferase system (PTS), which is believed to be used for fructose transport [24, 25]. When C. saccharolyticus was cultivated on a mixture of monosaccharides, they were consumed simultaneously but at different rates, i.e., fructose > arabinose > xylose > mannose > glucose > galactose. Unlike the case with disaccharides, the ABC transporters were not substrate specific for these monosaccharides. Instead, the affinity for the different sugars varied, with a clear preference for pentose sugars. Overall, the genome and transcription analyses revealed that C. saccharolyticus is well equipped for utilizing complex carbohydrates, such as starch and lignocellulosic polysaccharides .
For cost-efficient biohydrogen production, it is critical to achieve high substrate-conversion efficiencies due to the central cost of the raw material and the need to reduce the chemical oxygen demand (COD) in the waste stream . Strategies to improve the overall process yield include the application of hybrid two-step systems, consisting of a dark fermentation step combined with either a light fermentation step , or a methanogenesis step [4, 38]. In this way, the products of the first fermentation process, consisting mainly of volatile fatty acids, can be converted in the second step to either H2 and CO2 or CH4 and CO2, respectively. The pros and cons of these two strategies were evaluated in a recent review  and will not be treated herein. Instead, we will focus on H2 yields of the dark fermentation step.
4.1 Metabolic pathways for hydrogen production
Effect of growth temperature on H2 yield.
Opt T °C
Escherichia coli SR15
On the other hand, enterobacteria are only able to produce maximally 2 moles H2/mol hexose, since H2 is generated via the hydrolysis of formate being produced from glucose through the pyruvate formate lyase-catalyzed pyruvate oxidation (Figure 1C). Interestingly, even the introduction of a synthetic ferredoxin-mediated pyruvate-to-H2 pathway in E. coli resulted in low H2 yields (i.e., ~2 mol/mol hexose) . Some of the possible reasons why mesophilic bacteria can produce only 2 moles H2/mol hexose, despite being equipped with the relevant metabolic pathways, are revealed in the following sections.
4.2 Thermodynamic aspects
where ∆ G0'is the Gibbs free energy at standard conditions (kJ/mol), R is the gas constant (kJ/mol·K) and T the absolute temperature (K).
In general, extreme thermophiles reach higher H2 yields than mesophiles (Table 1) , and also at higher temperatures the critical PH2 is higher. For instance, at a temperature of 70˚C the critical PH2 is 0.173 kPa. However, this value is still well below 60 kPa, at which in practice C. saccharolyticus is still capable of producing 3.6-4.0 moles H2/mol glucose .
To understand this controversy, it is to be noticed that temperature is not the only factor influencing H2 generation. The ΔG ' of the H2-producing process is also a function of the type of cofactor involved and the ratio of reduced to oxidized cofactors . Each cofactor has a different formal potential, i.e., the E0'for Fdred/Fdox < NADPH/NADP < NADH/NAD [36, 38, 39], and unless the cofactor specificity of the involved hydrogenase is known, it is not possible to determine the thermodynamics of the system. C. saccharolyticus possesses two distinct hydrogenases, i.e., one NADH-dependent Fe-only hydrogenase (Csac_1860-1864) and one Fdred-dependent, membrane-associated NiFe hydrogenase (Csac_1540-1545) . Given that the formal potential of Fdred/Fdox (E0' approx. -400 mV) is close to that of H2 (E0'H2: -414 mV) , the Fd-dependent hydrogenase reaction is energetically favourable up to a PH2 of 39 kPa at standard conditions. However, this calculation is based on an approximation since the actual midpoint redox potential of Fd depends on the strain and the temperature . The actual midpoint redox potential for Fd at 70ºC in C. saccharolyticus is not known, but should be in the same order of magnitude as found in other related thermophilic bacteria. From the thermodynamic estimation, it is obvious that it is primarily the NADH-dependent Fe-only hydrogenase that is inhibited by elevated PH2. Consistently, the NADH-dependent Fe-only hydrogenase in Thermoanaerobacter tengcongensis was downregulated at high PH2, while the Fd-dependent hydrogenase was constitutively expressed, independently of the PH2.
Recently, Schut and Adams  characterized a novel type of Fe-only hydrogenase in Thermotoga maritima (TM1424-TM1426) that uses NADH and Fdred simultaneously. This novel bifurcating hydrogenase could therefore catalyze the unfavourable oxidation of NADH to H2 by using the exothermic oxidation of ferredoxin as a driving force. Interestingly, the Fe-only hydrogenase genes in C. saccharolyticus (Csac_1860, 1863-1864) show ≥ 50% sequence similarities to the bifurcating hydrogenase genes in Tm. maritima (TM1424-TM1426), but it remains to be investigated whether this hydrogenase in C. saccharolyticus possesses a bifurcating function. In fact, many of the thermophiles listed in Table 1 and several mesophilic clostridia possess a Fe-only hydrogenase-encoding genes with sequence similarity to TM1424-TM1426 in Tm. maritima. This observation could give a plausible explanation to the ability of these thermophiles to produce high H2 yields in well-sparged bioreactors.
The ratio of reduced to oxidized cofactors has also a significant impact on the thermodynamics of the system (Eq. 1), which was confirmed experimentally by Velt et al . In C. saccharolyticus, the NADH/NAD ratio changed six folds during growth-phase transition in batch cultures , and consequently the value of the critical PH2 for hydrogen production will also vary with the growth state of the organism. Similar observations were reported for Clostridium cellulolyticum, Cl. butyricum and Cl. acetobutylicum. Therefore, based on the reasoning above, the thermodynamic constraint might not be an absolute parameter for determining the critical PH2 for hydrogen production.
However, the generally higher H2 yields obtained by thermophilic organisms still implies that temperature has a significant impact. An intriguing question that arises is why these thermophiles have evolved for optimized H2 production. Resolving this phenomenon would aid in designing highly efficient H2 cell factories.
As discussed above, due to gaps in the knowledge on the redox system in C. saccharolyticus, the thermodynamic constraint cannot be used to estimate its tolerance to H2. For practical reasons, the PH2 in the gas phase is generally used as a measure for H2 tolerance. The critical value of PH2 (10-20 kPa) as found for C. saccharolyticus is often quoted in the literature, and is defined as the partial pressure of H2 at which lactate formation, an alternative way for reoxidizing NADH, is initiated . This critical PH2 was determined in batch cultures of C. saccharolyticus on sucrose using a closed bioreactor without sparging. However, in a similar experimental setup, but with xylose as the substrate, the critical PH2 was up to 60 kPa, upon which the metabolism shifted to lactate . A possible explanation for the observed discrepancy can be based on the difference in the organism's metabolic activity on the two substrates, i.e., the volumetric H2 productivity is lower on xylose than on sucrose which results in different concentrations of dissolved H2. The variation in the observed critical PH2 values can also be a consequence of a different distribution pattern of catabolic and anabolic fluxes on the two substrates, leading to different metabolite levels that modulate lactate dehydrogenase (LDH) activity . In that sense, the critical PH2 has no strict value, but will depend on the organism, the substrate and probably other environmental factors of the fermentation process. To make it more complicated, in batch cultures on glucose (5 g/L), lactate formation is triggered at the transition to the stationary phase, even though the PH2 was low (6.3 kPa) . Therefore, there are obviously other factors that initiate lactate formation , making its use as a proper criterion for defining the critical PH2 questionable. Despite lactate being formed, growth still continues, but rather in a linear than an exponential fashion . In addition, in continuous cultures of C. saccharolyticus on glucose, growth and H2 production were still observed at a PH2 of 67 kPa at a low dilution rate (0.05 h-1) .
Kraemer et al  could not find any coherent correlation between the sparging gas flow rate and H2 yield under different fermentation conditions. Due to this ambiguity, one may wonder whether PH2 is an appropriate parameter for inferring the critical H2 concentration for growth and hydrogen production. Indeed, Pauss et al  demonstrated in various bioreactor systems that the dissolved H2 easily supersaturates the liquid phase and its concentration is far from equilibrium with the gas phase. This can be attributed to the low solubility of H2 in water and that H2 production takes place in the liquid phase. The dissolved H2 concentration is a function of H2 productivity and the mass transfer rate , where the latter is a function of gas sparging rate and the stirring rate. A study with C. saccharolyticus in a pH and temperature controlled stirred tank reactor confirmed that the dissolved H2 concentration is a more indicative parameter for inhibition of H2 production . The supersaturation of H2 in the liquid enacts a decline in H2 productivity via a metabolic shift to lactate, which may be a mechanism to steer away from exceeding the critical dissolved H2 concentration at which growth is inhibited . To maintain a high productivity the dissolved H2 concentration should be kept low through increasing the mass transfer rate in the reactor, e.g. by using an appropriate sparging gas and/or proper reactor design.
Nonetheless, since data on dissolved H2 concentrations are scarce in the literature and PH2 is usually the determined parameter, the PH2 will continue to be used for comparisons in this review.
5.1 Hydrogen tolerance and sulphur reduction
Based on thermodynamics, the heterotrophic archaeon Pyrococcus furiosus, with its growth optimum near 100°C , should reach a higher H2 yield at higher PH2 than that obtained with C. saccharolyticus. This organism also has an unusual advantage in that its GAPDH counterpart, glyceraldehyde-3-phosphate: ferredoxin oxidoreductase (GAPOR), generates Fdred, which has an exceptionally low formal potential (E'Fd,100°C = -600 mV; ). Therefore, based only on thermodynamic constraints (Eq. 1; ), P. furiosus should be the least H2-inhibited anaerobe listed in Table 1. Yet, it produces only 2-3 moles H2/mol hexose, it is highly sensitive to an increase in PH2, and, when present, it prefers to reduce S0 instead of protons. In nature, low-PH2 environments are usually achievable for H2 producers living in symbiosis with hydrogenotrophic methanogens .
This preference for S0 can be explained by examining the physiological properties of its hydrogenases, of which P. furiosus possesses three distinct sets. It has two cytosolic NiFe-hydrogenases, which can reduce either protons to H2 or polysulphide to H2S, using NADPH as an electron donor. It also has a membrane-bound NiFe-hydrogenase, which can reduce protons to H2 using Fdred as an electron donor , with the unique capability of generating a proton motive force via proton translocation . Moreover, it has a NiFe-containing hydrogenase complex , but its physiological role is partly unknown. As a third set, the organism possesses a ferredoxin:NADP oxidoreductase (or sulphide dehydrogenase) that regulates product formation depending on the PH2. In other words, with increasing PH2, this enzyme becomes more active and decreases H2 production by transferring electrons from Fdred to either polysulphide or NADP . NADPH can then be used to reduce pyruvate to alanine, catalyzed by an NADPH-dependent glutamate dehydrogenase and alanine aminotransferase .
S0 reduction by Thermoanaerobacter tengcongensis enhances growth, and in its absence the organism is highly sensitive to H2 and growth is strongly inhibited at PH2 above 10 kPa . There are, however, Thermoanaerobacter species that are H2-tolerant, such as the ethanol-adapted T. thermosulfurigenes. This adapted strain is able to maintain growth at 1 atm H2 by redirecting its metabolism to ethanol, but its H2 yield is not higher than 50% of the Thauer limit .
Members of the genus Thermotoga, which are isolated from both shallow and deep sea hydrothermal vents rich in S0, are normally able to reduce either S0 or thiosulphate . The members of this genus display varying degrees of sensitivity to H2, but H2 inhibition can be generally relieved by the addition of S0, most likely as the result of a "detoxification" reaction . For instance, the Thermotoga sp. strains FjSS3.B1 and FjSS.B1 are both highly sensitive to H2 and the addition of S0 can re-establish their growth . Although not generally required for its growth, Tm. maritima is able to reduce S0, but does not respire it, decreasing its H2 yield by 40% . In a H2-pressurized reactor (H2/CO2, 80/20%; 300 kPa), however, growth of Tm. maritima cells was not observed unless S0 was added . Johnson et al  demonstrated that Tm. maritima was strongly inhibited by H2, which triggers the cells to enter stationary phase. Consistently, Schröder et al , demonstrated that PH2 levels above 2.3 kPa might be inhibitory to growth of Tm. maritima. However, since the organism was cultivated under uncontrolled conditions, other effects, such as the growth-associated drop in pH, might have contributed to growth inhibition. Although Marinitoga is closely related to Thermotoga, members of this genus can generally tolerate more H2 than Thermotoga species. For instance, M. hydrogenotolerans can grow at 1 atm H2 without any reduction in biomass yield, but then ethanol is formed under these conditions, which drains the electrons required for H2 production. In addition, in the presence of S0, H2 is not formed .
In contrast, members of the genus Caldicellulosiruptor are generally unable to reduce S0 or thiosulphate [29, 62, 63]. Moreover, both C. saccharolyticus and C. owensensis are capable of growing and producing H2 at PH2 levels up to 67 and 44 kPa, respectively [16, 66]. Similarly, growth of C. kristjanssonii was not inhibited at PH2 levels up to50 kPa .
The information gathered from the literature so far, in addition to our own work, reveals that S0-reducing thermophiles are generally more sensitive to H2 than thermophiles that are unable to use S0 as an electron acceptor. This conclusion supports the previously proposed correlation between the ability to reduce S0 and the sensitivity to H2 inhibition . Due to inconsistencies in the experimental design for the different microorganisms studied and the lack of data on dissolved H2 concentrations, one should be aware that it is difficult to quantify H2 tolerance. In conclusion, based on this knowledge, it can be suggested to select for non-S0-reducing H2-producing candidates and future attempts to isolate promising H2 producers should be targeting S0-poor environments.
5.2 H2 removal from the liquid
Comparison of different sparging conditions
Difficult to separate from H2 Expensive
Easily separated Produced in the process
Increases osmolarity Inhibits H2 productivity
Easily separated Produced in a hybrid biohydrogen/biogas process
No results available for C. saccharolyticus
No dilution of the gas
Expensive at large scale
Risk of contamination
No dilution of the gas
Inhibits H2 productivity
Inhibits H2 yield
Currently, N2 is commonly used as a sparging gas for lab-scale H2 production. However, applying this method at an industrial scale is not cost-effective since N2 is inert, and thus difficult to remove from the effluent gas stream . Instead, CO2 could be an appropriate alternative since it can be more readily separated from H2 and, as a convenience, it is a product of the fermentation process itself . Nevertheless, being chemically non inert, CO2 can influence the metabolism of some microorganisms as well as the composition of the culture medium, and hence may not be viewed as an adequate universal sparging gas. In C. saccharolyticus cultures, CO2 was already shown to negatively influence growth and H2 production rate . In that study, higher partial pressures of CO2 (PCO2) were found to increase the concentration of dissolved CO2, which is hydrolyzed to bicarbonate and protons. This requires the addition of larger amounts of a caustic agent to compensate for the decrease in pH, contributing to an increased osmotic pressure, which inhibits growth in C. saccharolyticus, and a higher environmental burden . Methane is another interesting alternative sparging gas that was previously shown to improve the H2 yield of a mesophilic consortium by 88% . However, the effect of this gas on H2 production by C. saccharolyticus has not been investigated yet.
Other strategies, such as applying reduced pressure to remove H2 and CO2 from the headspace, have been shown to efficiently increase H2 yields in Enterobacter cloacae at lab scale . However, on an industrial scale, this strategy might not be economically feasible due to high energy cost and increased contamination risk. Instead, two other alternative approaches may be pursued: i) improvement of reactor design to decrease the levels of dissolved H2 and CO2, and ii) metabolic engineering of the organism to enable it to either produce higher H2 yields at high PH2 or to withstand higher osmotic pressures.
Based on its genome sequence and transcriptome analysis, C. saccharolyticus appears to rely primarily on ABC transporters for sugar uptake [23, 26]. Bacterial and archaeal ABC transporters consist of five subunits, i.e., a sugar-binding protein, two transmembrane domains and two nucleotide-binding domains . A common characteristic of the sugar binding protein is its ability to capture the sugar outside the cell via a cap-lock mechanism, which determines the high affinity of the transporter for the substrate. Despite the large number of ABC transporters in C. saccharolyticus, none of them have been characterized so far. However, based on transcriptional analysis, it has been concluded that, in C. saccharolyticus, the same transporter might translocate different sugars with varying affinities [23, 26].
Theoretical ATP yield (YATP/S) (mol/mol) of anaerobic glucose oxidation with different transport systems and fermentation products.
The type of transport system with respect to growth temperature.
Opt T °C
6.1 PPi as an additional energy carrier
Another strategy to conserve energy employed by C. saccharolyticus is to utilize inorganic PPi as an additional energy carrier . This strategy is widely applied by anaerobes and other organisms that can acquire only low energy outputs in their metabolism to obtain sufficient ATP , of which Tm. maritima and various Clostridium species [72, 73] are a few examples that have been studied to some extent.
The primary sources of PPi are poly-nucleic acid biosynthesis from (deoxy)nucleotide triphosphates and activation of amino acids and fatty acids for protein and lipid synthesis, respectively, which are reactions that operate close to equilibrium. Therefore, subsequent PPi hydrolysis is required for driving these reactions forward . Moreover, studies on E. coli have shown that maintaining low PPi concentrations through effective PPi hydrolysis is required for rapid growth . In E. coli, as in a majority of other organisms, PPi hydrolysis is catalyzed by a cytosolic inorganic pyrophosphatase (PPase), with the dissipation of the free-energy change of the bound PPi (ΔG0'=-21.8 kJ/mol; ) as heat.
Interestingly, there are indications that the PPi-level follows the growth dynamics of C. saccharolyticus. When the cells were growing exponentially at the maximum growth rate, the PPi levels were relatively high (4 ± 2 mM), and when the growth rate decreased, the PPi levels declined concordantly. The dynamics in PPi levels were shown to be associated with the low cytosolic PPase activity in C. saccharolyticus. Consistently, the PPi levels followed the same growth-dependent trend in Moorella thermoacetica and Cl. pasteurianum, both of which also lack a cytosolic PPase . In contrast, in E. coli possessing elevated cytosolic PPase activity (0.54 U/mg cdw), the PPi levels were low (0.3 mM) and did not fluctuate during growth .
Unlike PPi, the ATP levels in C. saccharolyticus were very low (0.43 ± 0.07 mM) during the exponential growth phase, but increased 2 folds at the beginning of the stationary phase . Interestingly, the ADP concentration was higher than that of ATP during both phases , which is generally considered to be a sign of starvation. Similar low ATP/ADP ratios were observed in Cl. acetobutylicum. Nevertheless, C. saccharolyticus grew exponentially, suggesting that it relies on other energy carriers, such as PPi, that may contribute to its energy charge in addition to ATP .
6.2 Enzyme regulation
Regulation of the classical glycolysis and the flux distribution at the pyruvate node is a very complex and highly tuned process, since it is the principal provider of energy carriers and redox equivalents that need to be precisely balanced under all growth conditions. Regulation takes place at metabolite level as well as at enzyme and gene expression levels. Enzyme activities normally are regulated via direct mass action law (concentrations of substrates or effectors) or via allosteric inhibition or activation . To maintain high growth rate conditions, cells of C. saccharolyticus should obtain optimal energy gain from the substrate to fuel both anabolism and sugar transport, and thus lactate dehydrogenase (LDH) and alcohol dehydrogenase (ADH) should be kept inactive (Figure 2). Indeed, a recent batch-fermentation study has shown that during exponential growth, H2, CO2 and acetate are the only fermentation products in C. saccharolyticus. In this growth phase, neither ethanol nor lactate was formed, although both LDH and ADH activities were detected in crude cell extracts at high levels. However, as the growth rate decreased during transition to the stationary phase, the metabolism was partly directed towards lactate formation. Similar growth phase-related metabolic shifts have been observed in Cl. cellulolyticum. Studying the in vitro kinetics of LDH activity in C. saccharolyticus confirmed the observations of the batch experiments. It revealed that LDH activity in C. saccharolyticus is strongly regulated by the levels of the energy carriers PPi and ATP, in addition to the NADH/NAD ratio (Figure 2) . When the cells are growing at the maximum specific growth rate, PPi levels are high and ATP levels are low, keeping LDH inactive and its affinity for NADH low. It further assures that the catabolic flux is directed to acetate and H2 (Figure 2). However, as soon as the anabolic activity declines, the PPi/ATP ratio drops by an order of magnitude , which results in an increase in LDH activity as well as its affinity for NADH and hence lactate starts being formed .
Due to the strong control of C. saccharolyticus LDH activity at enzyme level, lactate is formed only in special cases, i.e., at elevated NADH/NAD ratios and at higher ATP levels. High NADH/NAD ratios also lead to inhibition of GAPDH activity and consequently the glycolytic flux [16, 47]. Since LDH activity secures the continuation of the glycolytic flux, through diminishing the NADH/NAD ratio, the enzyme can be considered essential for balanced growth in C. saccharolyticus. It thus might be questioned whether deleting the ldh gene would improve H2 yields during sugar fermentation. It might be a better approach to control lactate production through maintaining process conditions that promote exponential growth to keep high cellular PPi levels . It is worth noting that deletion of the ldh gene in E. coli only slightly increased H2 yield and productivities .
Ethanol is another reduced end product that is formed during growth of C. saccharolyticus, albeit in very low quantities (Figure 2; [13, 42]). Based on sequence similarities to the characterized ADH in T. ethanolicus, ADH in C. saccharolyticus possesses a NADPH-binding domain instead of a NADH-binding domain (Figure 2) . This observation is supported by a preliminary kinetic study showing that the affinity of the ADH of C. saccharolyticus for NADPH is higher than for NADH , indicating that ethanol and H2 formation do not compete for the same reduced cofactor.
13C-NMR analysis of intact cells has also revealed that C. saccharolyticus is capable of reducing either pyruvate or PEP to succinate (Figure 2) in the reductive branch of its incomplete TCA cycle. However, the succinate yield is significantly lower than that of acetate or lactate under regular growth conditions and might only operate under combined elevated PH2 and PCO2 levels .
Understanding the regulation of the key glycolytic enzyme GAPDH in C. saccharolyticus may also contribute to a better understanding of the organism's ability to tolerate elevated PH2. In general, GAPDH is strongly regulated by the NADH/NAD ratio , and GAPDH in C. saccharolyticus proved to be no exception . However, the enzyme in C. saccharolyticus is more resistant to increased NADH levels than GAPDH in most other related bacteria. The NADH concentration required for 50% inhibition of the enzyme in C. saccharolyticus was 0.03 mM, as compared to 0.01 mM in T. thermohydrosulfuricus (formerly known as Cl. thermohydrosulfuricum)  and Cl. acetobutylicum. This observation would in theory have a significant impact on the organism's tolerance to H2, i.e., if GAPDH was less inhibited by NADH, higher NADH/NAD ratios could be tolerated in the cell without affecting the glycolytic flux. As discussed above, this would also render the hydrogenase reaction more energetically favourable (Eq. 1) . Consistently, the ethanol-adapted T. thermohydrosulfuricus strain possesses a GAPDH that tolerates approximately twice the amount of NADH and is more tolerant to H2 than the wild-type strain . Likewise, the NADH/NAD ratio in Cl. cellulyticum is significantly higher than in C. saccharolyticus, which is possibly due to a more relaxed inhibition of its GAPDH by NADH (50% inhibition at 0.1 mM NADH) [42, 43].
C. saccharolyticus has several desirable characteristics needed for a H2 cell factory, such as its high H2 yields on a wide spectrum of carbon sources, its relatively high tolerance to elevated PH2, and its inability to reduce S0, which therefore does not interfere with its H2 production capabilities. However, the organism also lacks several properties, which should be considered before it can be used industrially.
7.1 Sensitivity to high osmolalities
Primarily, the sensitivity of C. saccharolyticus to increased osmotic pressures is a major drawback that should be addressed. The critical concentration of salts and solutes at which the growth of the organism ceases completely was estimated to be 400-425 mM . Osmolalities above 0.218 osm/kg H2O were found to induce cell lysis in C. saccharolyticus, as indicated by increased protein and DNA concentrations in the culture supernatant . This low osmotolerance imposes limitations on sparging the culture with CO2 and on the maximum sugar concentration in the medium , with the latter obviously having a negative effect on H2 productivity . On the other hand, the hyperthermophiles Tm. neapolitana and P. furiosus can grow optimally in the presence of 0.46 M NaCl and 0.5 M NaCl, respectively [82, 83]. These salt concentrations correspond to an additional 0.92 and 1 osm/kg H2O, respectively, in the culture media, demonstrating that these two hyperthermophiles are better protected against osmotic stress than C. saccharolyticus. This higher osmotic tolerance is due to their ability to produce compatible solutes, or osmoprotectants, such as β-mannosylglycerate, di-myo-insitol phosphate and glutamate [82, 83]. It remains to be investigated whether C. saccharolyticus is also able to efficiently synthesize similar solutes when exposed to osmotic stress. The low salt concentration in its natural habitat  may have resulted in the loss of any capability to survive in an unfavourable osmotic environment . However, the presence of biosynthetic genes for some osmoprotectants, such as proline and glutamate, could open the way for directed evolution to render C. saccharolyticus more osmotolerant .
7.2 Low productivities
The low cell density of cultures of C. saccharolyticus and other thermophiles, is another major drawback for industrial-scale application. It results in a low volumetric H2 productivity , unless dialysis or cell-recycling methods are used to increase the cell mass . Especially dialysis was found to increase the cell density of Pyrococcus furiosus by an order of magnitude, indicating that the presence of metabolic products prevents the increase in cell densities. In continuous cultures of C. saccharolyticus, the volumetric productivity could be enhanced by increasing the dilution rates, but this comes at the expense of the H2 yield [13, 85]. The decrease in yield could be related to increased dissolved H2 concentrations resulting from higher H2 productivities. This can inhibit the hydrogenase activity and ultimately results in a metabolic shift to lactate. The same trade off between yield and productivity was also observed with other microorganisms. For instance, E. coli produces much lower H2 yields but its volumetric productivity is almost 100-fold higher than in C. saccharolyticus[13, 86]. The cell density is about 200 times higher for E. coli than for C. saccharolyticus, which contributes considerably to the higher volumetric productivity. The specific H2 productivity of E. coli, however, is low, which could be an undesirable consequence of the higher cell number, i.e., it enhances the H2 mass-transfer resistance .
7.3 Biofilm formation and reactor design
Since C. saccharolyticus exhibits a relatively high specific H2 productivity, its volumetric production rate can potentially be enhanced through increasing its cell density  by, for example, inducing biofilm formation. The reactor configuration is an important factor in enhancing biofilm formation. So far, most research on C. saccharolyticus has been carried out in continuously stirred tank reactors (CSTR) [2, 13, 14, 85], which do not allow for efficient biomass retention. Alternative reactors that enhance biofilm formation include trickling-bed bioreactors  and fluidized-bed systems with granules . Trickling-bed bioreactors promote biofilm growth by means of packing material with a high surface area within the trickling bed. The liquid passes continuously through the filter, such that it guarantees a good liquid-gas exchange. In the fluidized-bed system, the biofilm is also formed as granules. This reactor system increases the turbulence, thus providing an enhanced mass transfer, which potentially also could decrease the dissolved H2 concentration, and hence, improve H2 yields. It should be noted that the biofilm mode of growth also offers the surface-attached and matrix-encased bacteria a means of protection against several stressful environmental conditions , which could benefit an organism like C. saccharolyticus in tolerating higher osmotic pressures. Recently, another Caldicellulosiruptor sp., viz. Caldicellulosiruptor owensensis, was shown capable of biofilm formation in both trickling-bed and fluidized-bed reactors at 70°C . Moreover, the organism retained its ability to grow and produce H2 in the fluidized-bed system even in complete absence of gas sparging.
This review article has focused on C. saccharolyticus as having several desirable characteristics for efficient H2 production. This is not only due to the high growth temperature of this organism, but there are strong indications that its metabolic constitution is adapted to efficiently extract energy from carbohydrates, thereby allowing the production of H2 at yields close to the Thauer limit . The energy metabolism of C. saccharolyticus, based on maximum ATP production per sugar unit and the use of PPi as an alternative energy carrier, might be correlated with the vast number of ABC transporters it employs. The efficiency of the energy metabolism is further illustrated by the modulation of LDH activity in C. saccharolyticus through the levels of the energy carriers ATP and PPi ; an active LDH will significantly lower the ATP production flux and thus the growth and H2 production rates, in addition to draining the electrons required for H2 production.
C. saccharolyticus can simultaneously co-utilize a wide variety of different sugars  and produces efficient extracellular hydrolytic enzymes, including cellulases . It has a relatively high tolerance to partial hydrogen pressures that might be related to its inability to reduce S0.
The set of capabilities of C. saccharolyticus described above is the foundation to exploit this organism in a commercial process using various raw materials . However, for obvious economical reasons the performance of C. saccharolyticus needs to be further improved, i.e., both high H2 yields and productivities should be obtained at relatively high PH2.
Several metabolic engineering strategies can be foreseen to improve H2 yields of C. saccharolyticus beyond 3.5 mol/mol hexose, without the need for gas sparging. First, the NADH-dependent GAPDH in C. saccharolyticus could be replaced with an Fd-dependent GAPOR, similar to the one in P. furiosus making the corresponding H2-generation reaction spontaneous even at elevated PH2[9, 36]. Second, introducing the genes for the oxidative part of the PPP supplemented with an NADPH-dependent hydrogenase could allow the oxidation of one mole of hexose to one mole of acetate and four moles of CO2[14, 90]. This would in theory yield 8 mol H2/mol hexose, but would not help overcome the thermodynamic barrier.
C. saccharolyticus exhibits a considerably high specific H2 production rate compared to other H2 producers , but poor volumetric productivities are obtained since its maximum cell densities is in the range of 108-109 cells/mL . Strategies to increase the cell density by at least an order of magnitude would be through inducing biofilm formation and/or increasing the substrate concentration. The latter requires strains with at least 5-fold increased osmotolerance, which might be obtained through evolutionary engineering. It is noteworthy that C. saccharolyticus possesses all the essential genes necessary for biosynthesis of compatible solutes, such as glutamate and proline .
As a technical approach, oversaturation of H2 in the liquid phase should be avoided to stabilize the fermentation process. This can be solved by smart reactor design and process configuration. Different membrane reactors have been developed, which are capable of reducing dissolved H2 concentrations and have a positive effect on H2 yields [91–94]. Yet, it remains to be investigated how C. saccharolyticus would perform in these reactor systems.
All in all, it is vital to understand the physiology of H2 production, which can be facilitated through applying genetic engineering and state-of-the-art 'omics' tools. However, so far, genetic protocols have been developed only for a few thermophilic hydrogen producers [95–98], but not yet for C. saccharolyticus. Omics-based technologies are increasingly applied for studying thermophilic H2 producers [25, 99, 100], including C. saccharolyticus[24, 25]. Together with genome-wide metabolic models, now being developed for some thermophiles [101, 102], the systems biology approach can eventually be applied to accelerate our understanding of the physiology of C. saccharolyticus and other thermophiles to increase their potential for process applications.
The insights in the physiology of C. saccharolyticus, as covered in this review, should contribute to better strategies for the isolation and/or engineering of future superior H2 producers. Creating a superior H2 cell factory is a quintessential step towards a sustainable biological H2 production.
AAZ acknowledges support from the Ministry of Higher Education in Egypt. The research on biohydrogen production in our lab is financially supported by the Commission of European Communities, Sixth Framework Program, Priority 6, Sustainable Energy Systems (019825 HYVOLUTION) and the Swedish Energy Agency (Energimyndigheten; 31090-1).
- Claassen PAM, van Lier JB, Contreras AML, van Niel EWJ, Sijtsma L, Stams AJM, de Vries SS, Weusthuis RA: Utilisation of biomass for the supply of energy carriers. Appl Microbiol Biotechnol. 1999, 52: 741-755. 10.1007/s002530051586.Google Scholar
- de Vrije T, Bakker RR, Budde MAW, Lai MH, Mars AE, Claassen PAM: Efficient hydrogen production from the lignocellulosic energy crop Miscanthus by the extreme thermophilic bacteria Caldicellulosiruptor saccharolyticus and Thermotoga neapolitana. Biotech Biofuels. 2009, 2: 12-10.1186/1754-6834-2-12.Google Scholar
- Jen CJ, Chou CH, Hsu PC, Yu SJ, Chen WE, Lay JJ, Huang CC, Wen FS: Flow-FISH analysis and isolation of clostridial strains in an anaerobic semi-solid bio-hydrogen producing system by hydrogenase gene target. Appl Microbiol Biotechnol. 2007, 74: 1126-1134. 10.1007/s00253-006-0740-8.Google Scholar
- Ueno Y, Otsuka S, Morimoto M: Hydrogen production from industrial wastewater by anaerobic microflora in chemostat culture. J Ferment Bioeng. 1996, 82: 194-197. 10.1016/0922-338X(96)85050-1.Google Scholar
- Liu D, Zeng RJ, Angelidaki I: Hydrogen and methane production from household solid waste in the two-stage fermentation process. Water Res. 2006, 40: 2230-2236. 10.1016/j.watres.2006.03.029.Google Scholar
- Hallenbeck PC, Ghosh D: Advances in fermentative biohydrogen production: the way forward?. Trends Biotechnol. 2009, 27: 287-297. 10.1016/j.tibtech.2009.02.004.Google Scholar
- Kovács KL, Maróti G, Rákhely G: A novel approach for biohydrogen production. Int J Hydrogen Energy. 2006, 31: 1460-1468. 10.1016/j.ijhydene.2006.06.011.Google Scholar
- Claassen PAM, de Vrije T: Non-thermal production of pure hydrogen from biomass: HYVOLUTION. Int J Hydrogen Energy. 2006, 31: 1416-1423. 10.1016/j.ijhydene.2006.06.006.Google Scholar
- Thauer RK, Jungermann K, Decker K: Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev. 1977, 41: 100-180.Google Scholar
- Stams AJM: Metabolic interactions between anaerobic bacteria in methanogenic environments. Antonie Van Leeuwenhoek. 1994, 66: 271-294. 10.1007/BF00871644.Google Scholar
- van Groenestijn JW, Hazewinkel JHO, Nienoord M, Bussmann PJT: Energy aspects of biological hydrogen production in high rate bioreactors operated in the thermophilic temperature range. Int J Hydrogen Energy. 2002, 27: 1141-1147. 10.1016/S0360-3199(02)00096-4.Google Scholar
- Kleerebezem R, van Loosdrecht MCM: Mixed culture biotechnology for bioenergy production. Curr Opin Biotechnol. 2007, 18: 207-212. 10.1016/j.copbio.2007.05.001.Google Scholar
- Kengen SWM, Goorissen HP, Verhaart M, van Niel EWJ, Claassen PAM, Stams AJM: Biological hydrogen production by anaerobic microorganisms. Biofuels. Edited by: Soetaert W, Vandamme EJ. 2009, 197-221. full_text. Chichester: John Wiley & SonsGoogle Scholar
- de Vrije T, Mars AE, Budde MA, Lai MH, Dijkema C, de Waard P, Claassen PAM: Glycolytic pathway and hydrogen yield studies of the extreme thermophile Caldicellulosiruptor saccharolyticus. Appl Microbiol Biotechnol. 2007, 74: 1358-1367. 10.1007/s00253-006-0783-x.Google Scholar
- van Niel EWJ, Budde MAW, de Haas GG, van der Wal FJ, Claassen PAM, Stams AJM: Distinctive properties of high hydrogen producing extreme thermophiles, Caldicellulosiruptor saccharolyticus and Thermotoga elfii. Int J Hydrogen Energy. 2002, 27: 1391-1398. 10.1016/S0360-3199(02)00115-5.Google Scholar
- Willquist K: Physiology of Caldicellulosiruptor saccharolyticus: a hydrogen cell factory. 2010, PhD thesis Lund University, Applied MicrobiologyGoogle Scholar
- Gibbs MD, Reeves RA, Farrington GK, Anderson P, Williams DP, Bergquist PL: Multidomain and multifunctional glycosyl hydrolases from the extreme thermophile Caldicellulosiruptor isolate Tok7B.1. Curr Microbiol. 2000, 40: 333-340. 10.1007/s002849910066.Google Scholar
- Park AR, Oh DK: Effects of galactose and glucose on the hydrolysis reaction of a thermostable beta-galactosidase from Caldicellulosiruptor saccharolyticus. Appl Microbiol Biotechnol. 2009, 85: 1427-1435. 10.1007/s00253-009-2165-7.Google Scholar
- Morris DD, Gibbs MD, Ford M, Thomas J, Bergquist PL: Family 10 and 11 xylanase genes from Caldicellulosiruptor sp strain Rt69B.1. Extremophiles. 1999, 3: 103-111. 10.1007/s007920050105.Google Scholar
- Dwivedi PP, Gibbs MD, Saul DJ, Bergquist PL: Cloning, sequencing and overexpression in Escherichia coli of a xylanase gene, xynA from the thermophilic bacterium Rt8B.4 genus Caldicellulosiruptor. Appl Microbiol Biotechnol. 1996, 45: 86-93. 10.1007/s002530050653.Google Scholar
- Bergquist PL, Gibbs MD, Morris DD, Te'o VS, Saul DJ, Moran HW: Molecular diversity of thermophilic cellulolytic and hemicellulolytic bacteria. FEMS Microbiol Ecol. 1999, 28: 99-110. 10.1111/j.1574-6941.1999.tb00565.x.Google Scholar
- Ivanovaa G, Rakhely G, Kovacs KL: Hydrogen production from biopolymers by Caldicellulosiruptor saccharolyticus and stabilization of the system by immobilization. Int J Hydrogen Energy. 2008, 33: 6953-6961. 10.1016/j.ijhydene.2008.08.058.Google Scholar
- Kadar Z, De Vrije T, Budde MA, Szengyel Z, Reczey K, Claassen PAM: Hydrogen production from paper sludge hydrolysate. Appl Biochem Biotechnol. 2003, 105-108: 557-566. 10.1385/ABAB:107:1-3:557.Google Scholar
- Van Fossen AL, Verhaart MR, Kengen SWM, Kelly RM: Carbohydrate utilization patterns for the extremely thermophilic bacterium Caldicellulosiruptor saccharolyticus reveal broad growth substrate preferences. Appl Environ Microbiol. 2009, 25: 7718-7724. 10.1128/AEM.01959-09.Google Scholar
- van de Werken HJG, Verhaart MRA, van Fossen AL, Willquist K, Lewis DL, Nichols JD, Goorissen HP, Mongodin EF, Nelson KE, van Niel EWJ, Stams AJM, Ward DE, de Vos WM, van der Oost J, Kelly RM, Kengen SWM: Hydrogenomics of the extremely thermophilic bacterium Caldicellulosiruptor saccharolyticus. Appl Environ Microbiol. 2008, 74: 6720-6729. 10.1128/AEM.00968-08.Google Scholar
- Kataeva IA, Yang SJ, Dam P, Poole FL, Yin Y, Zhou F, Chou WC, Xu Y, Goodwin L, Sims DR, Detter JC, Hauser LJ, Westpheling J, Adams MW: Genome sequence of the anaerobic, thermophilic, and cellulolytic bacterium "Anaerocellum thermophilum" DSM 6725. J Bacteriol. 2009, 191: 3760-3761. 10.1128/JB.00256-09.Google Scholar
- Yang SJ, Kataeva I, Wiegel J, Yin Y, Dam P, Xu Y, Westpheling J, Adams MWW: Reclassification of 'Anaerocellum thermophilum' as Caldicellulosiruptor bescii strain DSM 6725T sp. nov. Int J Syst Evol Microbiol. 2009, 60: 2011-2015. 10.1099/ijs.0.017731-0.Google Scholar
- Sissons CH, Sharrock KR, Daniel RM, Morgan HW: Isolation of cellulolytic anaerobic extreme thermophiles from New-Zealand thermal sites. Appl Environ Microbiol. 1987, 53: 832-838.Google Scholar
- Bergquist PL, Gibbs MD, Saul DJ, Te'o VSJ: Molecular genetics of thermophilic bacterial genes coding for enzymes involved in cellulose and hemicellulose degradation. Genetics, biochemistry and ecology in biodegradation of lignocellulose. Edited by: Shimada K, Hoshino S, Ohmiya K, Sakka K, Kobayashi Y, Karita S. 1993, 276-285. Tokyo: Uni PublishersGoogle Scholar
- van Niel EWJ, Claassen PAM, Stams AJM: Substrate and product inhibition of hydrogen production by the extreme thermophile, Caldicellulosiruptor saccharolyticus. Biotechnol Bioeng. 2003, 81: 255-262. 10.1002/bit.10463.Google Scholar
- Willquist K, Claassen PAM, van Niel EWJ: Evaluation of the influence of CO2 on hydrogen production by Caldicellulosiruptor saccharolyticus. Int J Hydrogen Energy. 2009, 34: 4718-4726. 10.1016/j.ijhydene.2009.03.056.Google Scholar
- Rainey FA, Donnison AM, Janssen PH, Saul D, Rodrigo A, Bergquist PL, Daniel RM, Stackebrandt E, Morgan HW: Description of Caldicellulosiruptor saccharolyticus gen-nov, sp. nov. an obligately anaerobic, extremely thermophilic, cellulolytic bacterium. FEMS Microbiol Lett. 1994, 120: 263-266. 10.1111/j.1574-6968.1994.tb07043.x.Google Scholar
- Levin DB, Carere CR, Cicek N, Sparling R: Challenges for biohydrogen production via direct lignocellulose fermentation. Int J Hydrogen Energy. 2009, 34: 7390-7403. 10.1016/j.ijhydene.2009.05.091.Google Scholar
- Panagiotopoulos IA, Bakker RR, de Vrije T, Urbaniec K, Koukios EG, Claassen PAM: Prospects of utilization of sugar beet carbohydrates for biological hydrogen production in the EU. J Clean Prod. 2010, 18: S9-S14. 10.1016/j.jclepro.2010.02.025.Google Scholar
- Ivanova G, Rakhely G, Kovacs KL: Thermophilic biohydrogen production from energy plants by Caldicellulosiruptor saccharolyticus and comparison with related studies. Int J Hydrogen Energy. 2009, 34: 3659-3670. 10.1016/j.ijhydene.2009.02.082.Google Scholar
- Cantarel BL, Coutinho PM, Rancurel C, Bernard T, Lombard V, Henrissat B: The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics. Nucleic Acids Research. 2009, 37: D233-D238. 10.1093/nar/gkn663.Google Scholar
- Uyar B, Eroglu I, Yucel M, Gunduz U: Photofermentative hydrogen production from volatile fatty acids present in dark fermentation effluents. Int J Hydrogen Energy. 2009, 34: 4517-4523. 10.1016/j.ijhydene.2008.07.057.Google Scholar
- Ueno Y, Fukui H, Goto M: Operation of a two-stage fermentation process producing hydrogen and methane from organic waste. Environ Sci Technol. 2007, 41: 1413-1419. 10.1021/es062127f.Google Scholar
- Hallenbeck PC: Fundamentals of the fermentative production of hydrogen. Water Sci Technol. 2005, 52: 21-29.Google Scholar
- Akhtar MK, Jones PR: Construction of a synthetic YdbK-dependent pyruvate:H2 pathway in Escherichia coli BL21(DE3). Metab Eng. 2009, 11: 139-147. 10.1016/j.ymben.2009.01.002.Google Scholar
- Angenent LT, Karim K, Al-Dahhan MH, Domiguez-Espinosa R: Production of bioenergy and biochemicals from industrial and agricultural wastewater. Trends Biotechnol. 2004, 22: 477-485. 10.1016/j.tibtech.2004.07.001.Google Scholar
- Kraemer JT, Bagley DM: Supersaturation of dissolved H2 and CO2 during fermentative hydrogen production with N2 sparging. Biotechnol Lett. 2006, 28: 1485-1491. 10.1007/s10529-006-9114-7.Google Scholar
- Velt A, Kallm AM, Mizutani T, Jones PR: Constructing and testing the thermodynamic limits of synthetic NAD(P)H:H2 pathways. Microbiol Biotechnol. 2008, 1: 382-394. 10.1111/j.1751-7915.2008.00033.x.Google Scholar
- Smith ET, Blamey JM, Zhou ZH, Adams MWW: A variable-temperature direct electrochemical study of metalloproteins from hyperthermophilic microorganisms involved in hydrogen production from pyruvate. Biochemistry. 1995, 34: 7161-7169. 10.1021/bi00021a030.Google Scholar
- Soboh B, Linder D, Hedderich R: A multisubunit membrane-bound [NiFe] hydrogenase and an NADH-dependent Fe-only hydrogenase in the fermenting bacterium Thermoanaerobacter tengcongensis. Microbiology. 2004, 150: 2451-2463. 10.1099/mic.0.27159-0.Google Scholar
- Schut GJ, Adams MWW: The iron-hydrogenase of Thermotoga maritima utilizes ferredoxin and NADH synergistically: a new perspective on anaerobic hydrogen production. J Bacteriol. 2009, 191: 4451-4457. 10.1128/JB.01582-08.Google Scholar
- Willquist K, van Niel EWJ: Lactate formation in Caldicellulosiruptor saccharolyticus is regulated by the energy carriers pyrophosphate and ATP. Metab Eng. 2010, 12: 282-290. 10.1016/j.ymben.2010.01.001.Google Scholar
- Payot S, Guedon E, Gelhaye E, Petitdemange H: Induction of lactate production associated with a decrease in NADH cell content enables growth resumption of Clostridium cellulolyticum in batch cultures on cellobiose. Res Microbiol. 1999, 150: 465-473. 10.1016/S0923-2508(99)00110-2.Google Scholar
- Abbad Andaloussi S, Durr C, Raval G, Petitdemange H: Carbon and electron flow in Clostridium butyricum grown in chemostat culture on glycerol and on glucose. Microbiology. 1996, 142: 1149-1158. 10.1099/13500872-142-5-1149.Google Scholar
- Meyer CL, Papoutsakis ET: Increased Levels of ATP and NADH are associated with increased solvent production in continuous cultures of Clostridium acetobutylicum. Appl Microbiol Biotechnol. 1989, 30: 450-459. 10.1007/BF00263849.Google Scholar
- Kraemer JT, Bagley DM: Improving the yield from fermentative hydrogen production. Biotechnol Lett. 2007, 29: 685-695. 10.1007/s10529-006-9299-9.Google Scholar
- Pauss A, Andre G, Perrier M, Guiot SR: Liquid-to-gas mass transfer in anaerobic processes: inevitable transfer limitations of methane and hydrogen in the biomethanation process. Appl Environ Microbiol. 1990, 56: 1636-1644.Google Scholar
- Fiala G, Stetter KO: Pyrococcus furiosus sp-nov represents a novel genus of marine heterotrophic archaebacteria growing optimally at 100 degrees C. Arch Microbiol. 1986, 145: 56-61. 10.1007/BF00413027.Google Scholar
- Mukund S, Adams MWW: Glyceraldehyde-3-phosphate ferredoxin oxidoreductase, a novel tungsten-containing enzyme with a potential glycolytic role in the hyperthermophilic archaeon Pyrococcus furiosus. J Biol Chem. 1995, 270: 8389-8392. 10.1074/jbc.270.15.8389.Google Scholar
- Kengen SWM, Stams AJM: Growth and energy conservation in batch cultures of Pyrococcus furiosus. FEMS Microbiol Lett. 1994, 117: 305-309. 10.1111/j.1574-6968.1994.tb06784.x.Google Scholar
- Sapra R, Bagramyan K, Adams MWW: A simple energy-conserving system: proton reduction coupled to proton translocation. Proc Natl Acad Sci USA. 2003, 100: 7545-7550. 10.1073/pnas.1331436100.Google Scholar
- Kengen SWM, Stams AJM: Formation of L-alanine as a reduced end-product in carbohydrate fermentation by the hyperthermophilic archaeon Pyrococcus furiosus. Arch Microbiol. 1994, 161: 168-175. 10.1007/BF00276479.Google Scholar
- Lovitt RW, Shen GJ, Zeikus JG: Ethanol production by thermophilic bacteria - biochemical basis for ethanol and hydrogen tolerance in Clostridium thermohydrosulfuricum. J Bacteriol. 1988, 170: 2809-2815.Google Scholar
- Adams MWW: The metabolism of hydrogen by extremely thermophilic, sulfur-dependent bacteria. FEMS Microbiol Rev. 1990, 75: 219-237. 10.1111/j.1574-6968.1990.tb04096.x.Google Scholar
- Ravot G, Ollivier B, Fardeau ML, Patel BKC, Andrews KT, Magot M, Garcia JL: L-Alanine production from glucose fermentation by hyperthermophilic members of the domains Bacteria and Archaea: A remnant of an ancestral metabolism?. Appl Environ Microbiol. 1996, 62: 2657-2659.Google Scholar
- Janssen PH, Morgan HW: Heterotrophic sulfur reduction by Thermotoga sp strain Fjss3.B1. FEMS Microbiol Lett. 1992, 96: 213-218. 10.1111/j.1574-6968.1992.tb05419.x.Google Scholar
- Huber R, Langworthy TA, Konig H, Thomm M, Woese CR, Sleytr UB, Stetter KO: Thermotoga maritima sp. nov. represents a new genus of unique extremely thermophilic eubacteria growing up to 90 degrees Celcius. Arch Microbiol. 1986, 144: 324-333. 10.1007/BF00409880.Google Scholar
- Johnson MR, Conners SB, Montero CI, Chou CJ, Shockley KR, Kelly RM: The Thermotoga maritima phenotype is impacted by syntrophic interaction with Methanococcus jannaschii in hyperthermophilic coculture. Appl Environ Microbiol. 2006, 72: 811-818. 10.1128/AEM.72.1.811-818.2006.Google Scholar
- Schröder C, Selig M, Schönheit P: Glucose fermentation to acetate, CO2 and H2 in the anaerobic hyperthermophilic eubacterium Thermotoga maritima - Involvement of the Embden-Meyerhof Pathway. Arch Microbiol. 1994, 161: 460-470.Google Scholar
- Postec A, Le Breton C, Fardeau ML, Lesongeur FO, Pignet P, Querellou J, Ollivier B, Godfroy A: Marinitoga hydrogenitolerans sp nov., a novel member of the order Thermotogales isolated from a black smoker chimney on the Mid-Atlantic Ridge. Int J Syst Evolution Microbiol. 2005, 55: 1217-1221. 10.1099/ijs.0.63550-0.Google Scholar
- Zeidan AA, van Niel EWJ: A quantitative analysis of hydrogen production efficiency of the extreme thermophile Caldicellulosiruptor owensensis OLT. Int J Hydrogen Energy. 2010, 35: 1128-1137. 10.1016/j.ijhydene.2009.11.082.Google Scholar
- Bredholt S, Sonne-Hansen J, Nielsen P, Mathrani IM, Ahring BK: Caldicellulosiruptor kristjanssonii sp nov., a cellulolytic extremely thermophilic, anaerobic bacterium. Int J Syst Bacteriol. 1999, 49: 991-996. 10.1099/00207713-49-3-991.Google Scholar
- Mandal B, Nath K, Das D: Improvement of biohydrogen production under decreased partial pressure of H2 by Enterobacter cloacae. Biotechnol Lett. 2006, 28: 831-835. 10.1007/s10529-006-9008-8.Google Scholar
- Jones PM, George AM: The ABC transporter structure and mechanism: perspectives on recent research. Cell Molec Life Sciences. 2004, 61: 682-699. 10.1007/s00018-003-3336-9.Google Scholar
- Linton KJ, Higgins CF: Structure and function of ABC transporters: the ATP switch provides flexible control. Pflugers Arch - Eur J Physiol. 2007, 453: 555-567. 10.1007/s00424-006-0126-x.Google Scholar
- Bielen AAM, Willquist K, Engman J, van der Oost J, van Niel EWJ, Kengen SWM: Pyrophosphate as a central energy carrier in the hydrogen-producing extremely thermophilic Caldicellulosiruptor saccharolyticus. FEMS Microbiol Lett. 2010, 307: 48-54. 10.1111/j.1574-6968.2010.01957.x.Google Scholar
- Mertens E: Pyrophosphate-dependent phosphofructokinase, an anaerobic glycolytic enzyme. FEBS Lett. 1991, 285: 1-5. 10.1016/0014-5793(91)80711-B.Google Scholar
- Ding YR, Ronimus RS, Morgan HW: Thermotoga maritima phosphofructokinases: expression and characterization of two unique enzymes. J Bacteriol. 2001, 183: 791-794. 10.1128/JB.183.2.791-794.2001.Google Scholar
- Heinonen JK: Biological role of inorganic pyrophosphate. 2001, Boston/Dordrecht/London: Kluwer Academic PublishersGoogle Scholar
- Chen J, Brevet A, Fromant M, Leveque F, Schmitter JM, Blanquet S, Plateau P: Pyrophosphatase is essential for growth of Esherichia coli. J Bacteriol. 1990, 172: 5686-5689.Google Scholar
- Heinonen JK, Drake HL: Comparative assessment of inorganic pyrophosphate and pyrophosphatase levels of Escherichia coli, Clostridium pasteurianum and Clostridium thermoaceticum. FEMS Microbiol Lett. 1988, 52: 205-208. 10.1111/j.1574-6968.1988.tb02596.x.Google Scholar
- Girbal L, Soucaille P: Regulation of Clostridium acetobutylicum metabolism as revealed by mixed-substrate steady-state continuous cultures - role of NADH/NAD ratio and ATP Pool. J Bacteriol. 1994, 176: 6433-6438.Google Scholar
- Cornish Bowden A: Fundamentals of Enzyme kinetics. 2004, Marseilles: Portland Press, 3Google Scholar
- Sode K, Watanabe M, Makimoto H, Tomiyama M: Construction and characterization of fermentative lactate dehydrogenase Escherichia coli mutant and its potential for bacterial hydrogen production. Appl Biochem Biotechnol. 1999, 77-9: 317-323. 10.1385/ABAB:77:1-3:317.Google Scholar
- Burdette D, Zeikus JG: Purification of acetaldehyde dehydrogenase and alcohol dehydrogenases from Thermoanaerobacter ethanolicus 39e and characterization of the secondary alcohol dehydrogenase (2-segrees ADH) as a bifunctional alcohol dehydrogenase acetyl-CoA reductive thioesterase. Biochemical J. 1994, 302: 163-170.Google Scholar
- Garrigues C, Loubiere P, Lindley ND, Cocaign-Bousquet M: Control of the shift from homolactic acid to mixed-acid fermentation in Lactococcus lactis: predominant role of the NADH/NAD+ ratio. J Bacteriol. 1997, 179: 5282-5287.Google Scholar
- Santos H, da Costa MS: Compatible solutes of organisms that live in hot saline environments. Environ Microbiol. 2002, 4: 501-509. 10.1046/j.1462-2920.2002.00335.x.Google Scholar
- Chou CJ, Jenney FE, Adams MWW, Kelly RM: Hydrogenesis in hyperthermophilic microorganisms: implications for biofuels. Metab Eng. 2008, 10: 394-404. 10.1016/j.ymben.2008.06.007.Google Scholar
- Holst O, Manelius Å, Krahe M, Märkl H, Raven N, Sharp R: Thermophiles and fermentation technology. Comp BiochemPhysiol. 1997, 118: 415-422.Google Scholar
- Yoshida A, Nishimura T, Kawaguchi H, Inui M, Yukawa H: Enhanced hydrogen production from formic acid by formate hydrogen lyase-overexpressing Escherichia coli strains. Appl Environ Microbiol. 2006, 72: 1716-1716. 10.1128/AEM.72.2.1716.2006.Google Scholar
- Kotsopoulos TA, Zeng RJ, Angelidaki I: Biohydrogen production in granular up-flow anaerobic sludge blanket (UASB) reactors with mixed cultures under hyper-thermophilic temperature (70 degrees C). Biotechnol Bioeng. 2006, 94: 296-302. 10.1002/bit.20844.Google Scholar
- Flemming HC: Biofilms and environmental protection. Water Sci Technol. 1993, 27: 1-10.Google Scholar
- Peintner C, Zeidan AA, Schnitzhofer W: Bioreactor systems for thermophilic fermentative hydrogen production: evaluation and comparison of appropriate systems. J Cleaner Prod.Google Scholar
- Lynd LR, van Zyl WH, McBride JE, Laser M: Consolidated bioprocessing of cellulosic biomass: an update. Curr Opin Biotechnol. 2005, 16: 577-583. 10.1016/j.copbio.2005.08.009.Google Scholar
- Verhaart MRA, Bielen AAM, van der Oost J, Stams AJM, Kengen SWM: Hydrogen production by hyperthermophilic and extremely thermophilic bacteria and archaea: mechanisms for reductant disposal. EnvironTechnol. 2010, 31: 993-1003.Google Scholar
- Tanisho S, Suzuki Y, Wakao N: Fermentative hydrogen evolution by Enterobacter aerogenes strain E-82005. Int J Hydrogen Energy. 1987, 12: 623-627. 10.1016/0360-3199(87)90003-6.Google Scholar
- Kumar N, Das D: Continuous hydrogen production by immobilized Enterobacter cloacae IIT-BT 08 using lignocellulosic materials as solid matrices. Enzyme Microbiol Technol. 2001, 29: 280-287. 10.1016/S0141-0229(01)00394-5.Google Scholar
- Kataoka N, Miya A, Kiriyama K: Studies on hydrogen production by continuous culture system of hydrogen-producing anaerobic bacteria. Water Sci Technol. 1997, 36: 41-47.Google Scholar
- Chin HL, Chen ZS, Chou CP: Fedbatch operation using Clostridium acetobutylicum suspension culture as biocatalyst for enhancing hydrogen production. Biotechnol Prog. 2003, 19: 383-388. 10.1021/bp0200604.Google Scholar
- Peng H, Fu B, Mao Z, Shao W: Electrotransformation of Thermoanaerobacter ethanolicus JW200. Biotechnol Lett. 2006, 28: 1913-1917. 10.1007/s10529-006-9184-6.Google Scholar
- Sato T, Fukui T, Atomi H, Imanaka T: Improved and versatile transformation system allowing multiple genetic manipulations of the hyperthermophilic archaeon Thermococcus kodakaraensis. Appl Environ Microbiol. 2005, 71: 3889-3899. 10.1128/AEM.71.7.3889-3899.2005.Google Scholar
- Santangelo TJ, Cubonova L, Reeve JN: Shuttle vector expression in Thermococcus kodakaraensis: contributions of cis elements to protein synthesis in a hyperthermophilic archaeon. Appl Environ Microbiol. 2008, 74: 3099-3104. 10.1128/AEM.00305-08.Google Scholar
- Tyurin MV, Desai SG, Lynd LR: Electrotransformation of Clostridium thermocellum. Appl Environ Microbiol. 2004, 70: 883-890. 10.1128/AEM.70.2.883-890.2004.Google Scholar
- Conners SB, Montero CI, Comfort DA, Shockley KR, Johnson MR, Chhabra SR, Kelly RM: An expression-driven approach to the prediction of carbohydrate transport and utilization regulons in the hyperthermophilic bacterium Thermotoga maritima. J Bacteriol. 2005, 187: 7267-7282. 10.1128/JB.187.21.7267-7282.2005.Google Scholar
- Wang J, Xue Y, Feng X, Li X, Wang H, Li W, Zhao C, Cheng X, Ma Y, Zhou P, Yin J, Bhatnagar A, Wang R, Liu S: An analysis of the proteomic profile for Thermoanaerobacter tengcongensis under optimal culture conditions. Proteomics. 2004, 4: 136-150. 10.1002/pmic.200300504.Google Scholar
- Zhang Y, Thiele I, Weekes D, Li Z, Jaroszewski L, Ginalski K, Deacon AM, Wooley J, Lesley SA, Wilson IA, Palsson B, Osterman A, Godzik A: Three-dimensional structural view of the central metabolic network of Thermotoga maritima. Science. 2009, 325: 1544-1549. 10.1126/science.1174671.Google Scholar
- Roberts SB, Gowen CM, Brooks JP, Fong SS: Genome-scale metabolic analysis of Clostridium thermocellum for bioethanol production. BMC Syst Biol. 2010, 4: 31- 10.1186/1752-0509-4-31.Google Scholar
- Bothun GD, Knutson BL, Berberich JA, Strobel HJ, Nokes SE: Metabolic selectivity and growth of Clostridium thermocellum in continuous culture under elevated hydrostatic pressure. Appl Microbiol Biotechnol. 2004, 65: 149-157. 10.1007/s00253-004-1554-1.Google Scholar
- Munro SA, Zinder SH, Walker LP: The fermentation stoichiometry of Thermotoga neapolitana and influence of temperature, oxygen, and pH on hydrogen production. Biotechnol Prog. 2009, 25: 1035-1042. 10.1002/btpr.201.Google Scholar
- Hild HM, Stuckey DC, Leak DJ: Effect of nutrient limitation on product formation during continuous fermentation of xylose with Thermoanaerobacter ethanolicus JW200 Fe(7). Appl Microbiol Biotechnol. 2003, 60: 679-686.Google Scholar
- Kanai T, Imanaka H, Nakajima A, Uwamori K, Omori Y, Fukui T, Atomi H, Imanaka T: Continuous hydrogen production by the hyperthermophilic archaeon, Thermococcus kodakaraensis KOD1. J Biotechnol. 2005, 116: 271-282. 10.1016/j.jbiotec.2004.11.002.Google Scholar
- de Souza AM, Sutherland IW: Exopolysaccharide and storage polymer production in Enterobacter aerogenes type-8 strains. J Appl Bacteriol. 1994, 76: 463-468.Google Scholar
- Hutkins RW, Kashket ER: Phosphotransferase activity in Clostridium acetobutylicum from acidogenic and solventogenic phases of growth. Appl Environ Microbiol. 1986, 51: 1121-1123.Google Scholar
- Hernandez PE: Transport of D-glucose in Clostridium thermocellum ATCC-27405. J Gen Appl Microbiol. 1982, 28: 469-477. 10.2323/jgam.28.469.Google Scholar
- Galperin MY, Noll KM, Romano AH: The glucose transport system of the hyperthermophilic anaerobic bacterium Thermotoga neapolitana. Appl Environ Microbiol. 1996, 62: 2915-2918.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.