- Open Access
Development of a genetic system for the deep-sea psychrophilic bacterium Pseudoalteromonas sp. SM9913
© Yu et al.; licensee BioMed Central Ltd. 2014
- Received: 9 September 2013
- Accepted: 17 January 2014
- Published: 22 January 2014
Pseudoalteromonas species are a group of marine gammaproteobacteria frequently found in deep-sea sediments, which may play important roles in deep-sea sediment ecosystem. Although genome sequence analysis of Pseudoalteromonas has revealed some specific features associated with adaptation to the extreme deep-sea environment, it is still difficult to study how Pseudoalteromonas adapt to the deep-sea environment due to the lack of a genetic manipulation system. The aim of this study is to develop a genetic system in the deep-sea sedimentary bacterium Pseudoalteromonas sp. SM9913, making it possible to perform gene mutation by homologous recombination.
The sensitivity of Pseudoalteromonas sp. SM9913 to antibiotic was investigated and the erythromycin resistance gene was chosen as the selective marker. A shuttle vector pOriT-4Em was constructed and transferred into Pseudoalteromonas sp. SM9913 through intergeneric conjugation with an efficiency of 1.8 × 10-3, which is high enough to perform the gene knockout assay. A suicide vector pMT was constructed using pOriT-4Em as the bone vector and sacB gene as the counterselective marker. The epsT gene encoding the UDP-glucose lipid carrier transferase was selected as the target gene for inactivation by in-frame deletion. The epsT was in-frame deleted using a two-step integration–segregation strategy after transferring the suicide vector pMT into Pseudoalteromonas sp. SM9913. The ΔepsT mutant showed approximately 73% decrease in the yield of exopolysaccharides, indicating that epsT is an important gene involved in the EPS production of SM9913.
A conjugal transfer system was constructed in Pseudoalteromonas sp. SM9913 with a wide temperature range for selection and a high transfer efficiency, which will lay the foundation of genetic manipulation in this strain. The epsT gene of SM9913 was successfully deleted with no selective marker left in the chromosome of the host, which thus make it possible to knock out other genes in the same host. The construction of a gene knockout system for Pseudoalteromonas sp. SM9913 will contribute to the understanding of the molecular mechanism of how Pseudoalteromonas adapt to the deep-sea environment.
- Gene Knockout
- Selective Plate
- Homologous Fragment
- sacB Gene
- Intergeneric Conjugation
The deep-sea floor constitutes almost 60% of the earth’s surface , most of which is covered with fine-grained sediments . The deep-sea sediments are a greatly dynamic geo- and biosphere, where no light is present, the temperature is as low as −1°C to 4°C and the pressure is up to 1,100 bar . Despite these extreme conditions, various microorganisms flourish in deep-sea sediments. Approximately 13% of the total global bacteria have been found in the upper 10 cm of deep-sea sediments [3, 4], which play an important role in the deep-sea ecosystem.
The extreme characteristics of the deep-sea sediments have compelled various bacteria to evolve special features to adapt to the deep-sea environment. However, the molecular mechanism of deep-sea bacteria adapted to deep-sea sediments is still largely unknown. By far, only several strains, such as Photobacterium profundum SS9 and Shewanella piezotolerans WP3, have been well studied in their adaptation to the deep sea. Photobacterium profundum SS9, which was isolated from the Sulu Sea in Philippines at a depth of 2.5 km , was found to have many special genetic features in DNA replication, fidelity and structure [6, 7], as well as membrane integrity and fluidity [8–10] to adapt to the high-pressure environment by Tn5 gene replacement mutagenesis. The environmental adaptation mechanisms of Shewanella piezotolerans WP3, a bacterium isolated from a western Pacific Ocean sediment sample at a depth of 1914 m , was also studied in the genomic level . Furthermore, many genes of this strain were found to be regulated by cold shock , and the regulation of fatty acid biosynthesis and NAP-α system in response to different temperatures and pressures were studied by gene knockout [14, 15].
Pseudoalteromonas are widespread in various marine environments. Over 30 marine species with a large number of strains have been reported in this genus. Studies on these marine bacteria have suggested that they play important roles in marine ecosystem. However, by far in this genus, only one strain, Pseudoalteromonas haloplanktis TAC125 from the Antarctic seawater, has been reported to have a gene knockout genetic system . Pseudoalteromonas strains are also frequently encountered in the analysis of deep-sea sedimentary bacterial diversity [17–19], implying that some bacteria in this genus may also play an important role in deep-sea sediment ecosystem. Some Pseudoalteromonas strains isolated from deep-sea sediments have been shown to be good extracellular enzyme producers or exopolysaccharide (EPS) producers [18, 20–23]. It is reported that an electroporation transformation system was developed in Pseudoalteromonas sp. PS1M3 from deep-sea sediments . Nevertheless, gene deletion has not been performed in this strain. Thus, gene knockout genetic system has not yet constructed in a deep-sea Pseudoalteromonas strain. Due to the lack of such genetic systems, little is yet known how Pseudoalteromonas adapt to the deep-sea environment at molecular level.
Pseudoalteromonas sp. SM9913 (hereafter called SM9913), isolated from the deep-sea sediment at 1855 m depth near the Okinawa Trough , is a psychrophilic strain capable of producing a great quantity of proteases [20, 26, 27] and EPS . The genome of SM9913 has been sequenced, and some specific features implying how Pseudoalteromonas sp. SM9913 adapts to the deep-sea environment have been revealed in gene level . However, it is still difficult to verify the predicted features by experiments due to the lack of a genetic system in SM9913. Therefore, it is necessary to develop a genetic system for the reverse genetics in SM9913 to investigate the molecular mechanism of how this bacterium adapts to the deep-sea sedimentary environment. In this study, a conjugal transfer system with high efficiency was constructed, and a gene knockout system in SM9913 was developed with the epsT gene encoding the initial UDP-glucose lipid carrier transferase as the target.
Sensitivity of SM9913 to six antibiotics
Sensitivity of SM9913 to different antibiotics
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Construction of the conjugal transfer system with high efficiency
Generation of the epsT mutant strain
As shown in Figure 1B, the suicide vector pMT was constructed using pOriT-4Em as the bone vector by eliminating RepA and its flanking sequences, inserting fragments (up and down) that flanks the epsT gene, and adding counter selective marker sacB gene. sacB encodes levansucrase, whose activity will not permit the host to survive in sucrose-containing medium.
Effect of epsT knockout on the EPS production of SM9913
The epsT gene of SM9913 encodes the UDP-glucose lipid carrier transferase, which may play an important role in the EPS synthesis in SM9913. To determine the effect of epsT knockout on the EPS production of SM9913, wild-type SM9913 and the ΔepsT mutant were cultured in marine LB broth, and the EPS yields were measured. The EPS produced by wild SM9913 in marine LB broth were 96 mg/l, and those produced by the ΔepsT mutant were only 26 mg/l. Therefore, knockout of espT severely affected the EPS production of SM9913, indicating that epsT is an important gene involved in the EPS biosyntheis of SM9913. The residual level of EPS in the ΔepsT mutant suggests that there may be either other gene(s) homologous to epsT or other pathway involved in EPS biosynthesis in SM9913.
In genus Pseudoalteromonas, a gene knockout genetic system has been developed in psychrophilic Pseudoalteromonas haloplanktis TAC125 from the Antarctic seawater . In this study, a gene knockout genetic system was successfully developed in the deep-sea psychrophilic strain Pseudoalteromonas sp. SM9913. In the genetic system of Pseudoalteromonas haloplanktis TAC125, 4°C was used to select the transconjugants to avoid the growth of the donor cells [16, 33]. In contrast, the transconjugants of SM9913 could be obtained at a wide range of temperatures below 20°C without the growth of the donor cells. This can save time because SM9913 grows much faster at its optimal temperature 15-20°C than at 4°C. Moreover, a wide temperature range for transconjugant selection would be helpful for studying the function of genes related to cold-adaptation of psychrophilic bacteria. For some key genes associated with bacterial cold-adaptation, the disruption of them may make bacterial cells difficult to grow at temperature as low as 4°C, which would disable the selection of transconjugants that have undergone first or double cross-over. In SM9913, this situation can be avoided by selecting the transconjugants at 20°C.
Pseudoalteromonas sp. SM9913 is a model strain to study the mechanism of how Pseudoalteromonas adapt to extreme deep-sea environment. In this study, the antibiotic sensitivity of Pseudoalteromonas sp. SM9913 was investigated. Erythromycin was selected for the screening of the transconjugants and the mutants that have underwent the first homologous recombination. A conjugal transfer system was constructed in SM9913 with a wide range of selection temperatures below 20°C and a high transfer efficiency of 1.8 × 10-3, which is high enough for the genetic manipulation such as heterologous expression and gene knockout in Pseudoalteromonas strains. The epsT gene of SM9913 was successfully deleted with a two-step homologous recombination without introducing any selective marker, making it possible to knock out other genes in the same host. Thus, a method for gene knockout in Pseudoalteromonas sp. SM9913 was successfully constructed, which will facilitate the functional analysis of genes associated with the deep-sea environment adaption of Pseudoalteromonas.
Plasmids, bacterial strains and growth conditions
Strains and plasmids used in this study
Strains or plamids
Genotype or markers; characteristics and uses
Source or reference
Escherichia coli DH5α
supE 44, △lac U169 (θ80lacZ△M15) endA1, recA1, hsdR17, thi-1 l − gyrA96, relA1; gene cloning
Escherichia coli ET12567
dam, dcm, hsdM, hsdS, hsdR, cat, tet; donor for the conjugal transfer
Pseudoalteromonas sp. SM9913
tra, neo, RP4; a derivative of RK2 with a mutation in oriT
R6K-derived suicide plasmid containing Str and sacB; template for oriT and sacB amplification
Cryptic plasmid of Pseudoalteromonas sp. Bsi20429; template for RepA
EmR, pWV01 origin, expression vector for L. lactis; template for EmR amplification
Antibiotics sensitivity assay
Ampicillin, kanamycin, chloromycetin, erythromycin, tetracycline and streptomycin were used for the antibiotics sensitivity assay of SM9913. SM9913 was grown in marine LB broth at 20°C to late exponential phase, and then 1% of the culture was inoculated to marine LB broth containing one of the six antibiotics in the final concentration of 10 μg/ml, 50 μg/ml or 100 μg/ml. The culture containing no antibiotic was used as the control. The cultures were incubated at 20°C with shaking for 48 h, and then were collected to determine their absorbance of OD600 using a V550 spectrophotometer (Jasco, Japan).
Construction of the shuttle vector pOriT-4Em
Primers used in this article
Expected size (bp)
RepA and its flanking sequences
EmR in pOriT-4Em
Upstream homologous fragment of epsT
Downstream homologous fragment of epsT
EmR in pMT
Confirmation of the second recombination
Construction of the suicide vector for epsT gene knockout in SM9913
Construction of the suicide vector used for gene knockout was based on the shuttle vector pOriT-4Em. An 834 bp upstream homologous fragment was amplified from the upstream of SM9913 epsT gene using primers UPF/UPR and inserted into the Sal I and Bam HI sites in pOriT-4Em to replace the EmR fragment. A downstream homologous fragment was obtained by PCR from the downstream of SM9913 epsT gene using primers DnF/DnR. EmR gene with its promoter used as the selective marker for the first homologous recombination was amplified from pMG36e with the primers EmF/EmR. Primers DnR and EmF was reverse complement with introducing an Xba I site between the downstream homologous fragment and the EmR expression cassette. These two DNA fragments were fused by overlap PCR and Bam HI and Nhe I sites were introduced at the 5′ and 3′ ends, respectively. The overlapped PCR product was cloned into pOriT-4EM to replace the RepA and its flanking sequences. Finally, sacB gene containing its promoter used as the counter selective marker for the second homologous recombination was amplified from pKNG101 using primers sacBF/sacBR and inserted into the vector at the Nco I and Apa I sites. The constructed suicide vector for epsT gene knockout was named as pMT.
Construction of conjugal transfer system using pOriT-4Em
The shuttle vector pOriT-4Em was transferred from E. coli ET12567 (pUZ8002) cells (donor strain) to SM9913 (recipient strain) by interspecific conjugation. The donor cells were grown to logarithmic phase of OD600 ≈ 0.6 in LB broth containing ampicillin (100 μg/ml), chloromycetin (25 μg/ml) and kanamycin (100 μg/ml) and recipient strains were grown to logarithmic phase of OD600 ≈ 0.6 in marine LB broth. The cells were washed twice using LB broth for the donor and marine LB broth for the recipient, and then were mixed under different proportions (donor : recipient =1 : 100, 1 : 10, 1 : 5, 1 : 1, 10 : 1 and 100 : 1). The mixed cells were spread onto a sterile 0.45 μm-pore-size membrane laid on a marine LB plate, which was then incubated at 20°C for mating. After 24 h, the cells were resuspended in 1 ml marine LB medium and spread onto marine LB plates containing 100 μg/ml erythromycin. The plates were incubated at 20°C for 36–48 h until the transconjugant colonies were visible. The transconjugants were inoculated into 5 ml marine LB broth containing 100 μg/ml erythromycin. After the cultures were shaken at 20°C overnight, plasmids were extracted using the High-purity Plasmid DNA Mini-preparation Kit (Bioteke, China).
To confirm that E. coli ET12567 could not survive on the selective plate at 20°C after mating with SM9913, the RepA gene in pOriT-4Em was disrupted by digestion with Nhe I and Xba I, and the derivative vector was named pOriT-4Em-ΔRepA, which could not replicate in SM9913. E. coli ET12567 harboring pOriT-4Em-ΔRepA was mixed with SM9913 under the proportion of 100 : 1. After mating at 20°C, the cells were spread onto marine LB plates containing 100 μg/ml erythromycin, which were then incubated at 20°C for at least 7 days. In the meantime, a control experiment was performed, in which E. coli ET12567 harboring pOriT-4Em-ΔRepA was mixed with marine LB medium and then spread onto the same selective plate, which was also incubated at 20°C for about 7 days until the colonies were visible.
The transfer efficiency was defined as the amount of transconjugants/the amount of donor cells in the mating assay.
Construction of the ΔepsT mutant strain
The suicide vector pMT was mobilized into SM9913 by interspecific conjugation. After mating, the cells were spread onto marine LB plates containing 100 μg/ml erythromycin to screen the clones in which a single recombination of pMT inserting into SM9913 genome occurred. The colonies were inoculated into 5 ml marine LB broth and shaken for 24 h, and then the pMT insertion mutants were verified by PCR using primers UPF/DnR after genomic DNA was extracted with the Bacterial DNA Extraction Kit (Bioteke, China). The mutants were then grown at 20°C with shaking in liquid marine LB broth containing no antibiotic, and the culture of late logarithmic phase was inoculated into 5 ml marine LB broth containing no antibiotic and grown at 20°C with shaking until OD600 was 0.6. To select the mutants in which the second recombination occurred, the culture was serially diluted, spread onto marine LB plates containing 30% sucrose, and grown at 20°C until colonies appeared. After the colonies were inoculated into 5 ml marine LB broth and shaken for 24 h, the genomic DNA of the mutants was extracted and PCR was performed to verify the recombination event to be back mutation or deletion mutation. The deletion mutation was then tested by southern blot hybridization.
Southern blot hybridization
Genomic DNA of the mutants was extracted with Bacterial DNA Extraction Kit and treated with the restriction endonuclease Hin dIII. The digested DNA was separated on 0.8% agarose gel by electrophoresis, and transferred to positively-charged nylon membrane (GE, UK) by capillary action. The probe containing part of epsT gene and its downstream was amplified from SM9913 genome DNA with primers EpsTF/DnR and labeled with digoxigenin-UTP. Detection of target DNA was performed using the DIG High Prime DNA Labeling and Detection kit (Roche, Switzerland) according to the manufacturer’s instructions.
Fermentation and yield determination of the EPS of SM9913 and its mutant
The EPS yields of SM9913 and its ΔepsT mutant in marine LB broth were determined. SM9913 and the mutant were grown in the medium at 15°C for 72 h with shaking. The cultures were then centrifuged (10,000 rpm, 10 min) and the supernatants were dialyzed in deionized water. The concentration of the EPS in the supernatants was determined using the phenol-sulfuric acid method as previously reported with glucose as standard .
The work was supported by the National Natural Science Foundation of China (grants 31290231, 91228210, 31025001, 31170055, 41176130, 81271896 and 31270064), the Hi-Tech Research and Development Program of China (grants 2011AA090703, 2011AA090704 and 2012AA092103), the China Ocean Mineral Resources R & D Association (COMRA) Special Foundation (grants DY125-15-T-05), the Special Fund of China for Marine-scientific Research in the Public Interest (grant 201005032–6).
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