Directly mining a fungal thermostable α-amylase from Chinese Nong-flavor liquor starter
© The Author(s) 2018
Received: 28 September 2017
Accepted: 12 February 2018
Published: 22 February 2018
Chinese Nong-flavor (NF) liquor is continuously and stably produced by solid-state fermentation technology for 1000 years, resulting in enrichment of special microbial community and enzymes system in its starter. Based on traditional culture-dependent methods, these functional enzymes are hardly obtained. According to our previous metatranscriptomic analysis, which identifies plenty of thermostable carbohydrate-active enzymes in NF liquor starter, the aim of this study is to provide a direct and efficient way to mine these thermostable enzymes.
In present study, an alpha-amylase (NFAmy13A) gene, which showed the highest expression level of enzymes in starch degradation at high temperature stage (62 °C), was directly obtained by functional metatranscriptomics from Chinese Nong-flavor liquor starter and expressed in Pichia pastoris. NFAmy13A had a typical signal peptide and shared the highest sequence identity of 64% with α-amylase from Aspergillus niger. The recombinant enzyme of NFAmy13A showed an optimal pH at 5.0–5.5 and optimal temperature at 60 °C. NFAmy13A was activated and stabilized by Ca2+, and its half-lives at 60 and 70 °C were improved significantly from 1.5 and 0.4 h to 16 and 0.7 h, respectively, in the presence of 10 mM CaCl2. Meanwhile, Hg2+, Co2+ and SDS largely inhibited its activity. NFAmy13A showed the maximum activity on amylopectin, followed by various starches, amylose, glycogen, and pullulan, and its specificity activity on amylopectin was 200.4 U/mg. Moreover, this α-amylase efficiently hydrolyzed starches (from corn, wheat, and potato) at high concentrations up to 15 mg/ml.
This study provides a direct way to mine active enzymes from man-made environment of NF liquor starter, by which a fungal thermostable α-amylase (NFAmy13A) is successfully obtained. The good characteristics of NFAmy13A in degrading starch at high temperature are consistent with its pivotal role in solid-state fermentation of NF liquor brewing. This work would stimulate mining more enzymes from NF liquor starter and studying their potentially synergistic roles in NF liquor brewing, thus paving the way toward the optimization of liquor production and improvement of liquor quality in future.
Chinese liquor accounts for more than one-third of all spirits consumed in the world according to the International Wine and Spirit Research Group. Chinese liquor is produced by a solid-state simultaneous saccharification and fermentation (SSF) in an environment-friendly way for 1000 years, and Nong-flavor (NF, also called strong aroma type) liquor accounts for more than 70% of Chinese liquor production [1, 2]. Its manufacture mainly contains two steps: 4 months of liquor starter (daqu) production and 40–45 days of alcohol solid-state fermentation [3, 4]. Special and stable microbial communities are enriched during the NF liquor starter production process , and in the mature NF liquor starter . These microbes would secret various enzymes, e.g., amylase, acid protease, cellulase, lipase, and esterase, to efficiently hydrolyze carbohydrates and proteins [7, 8].
Recently, great efforts have been made to mine enzymes by culture-independent method of metagenomics using either sequence-based or function-based screening from environmental systems, e.g. soil, rumen, ocean, spring, gut, activated sludge, skin surface, compost, most of which are from prokaryotic microbes . And, it is still very difficult to obtain enzymes of eukaryotic microorganisms from environments, due to difficulties in extracting polyadenylated messenger RNA (metatranscriptomics), and the lack of efficient and compatible hosts. At present time, only a few enzymes are reported to be identified by functional metatranscriptomics of eukaryotes from soil, rumen and the gut of the termite [10–13], or by sequence-based metatranscriptomics of eukaryotes from forest soil . Same as soil, eukaryotic microbial communities also play pivotal roles in man-made environmental NF liquor starter, since NF liquor starter is mainly made from wheat [3, 8]. However, in a long time, the complicities in this man-made environment of NF liquor starter, e.g., the high content of starch and other polysaccharides, thousands of fermentation products at high temperature, limit the acquisition and characterization of active enzymes from this environment, and only crude enzymes are analyzed until now . Recently, a breakthrough on NF liquor starter is made by metatranscriptomic analysis in our previous work, and it is found that fungi are the most abundant and active community members and total 932 carbohydrate-active enzymes are identified at the high temperature stage (N3) of 62 °C . Moreover, many active enzymes with whole length gene sequences are identified. Therefore, metatranscriptomic analysis provides a direct and efficient sequence-based method to mine these fungal functional enzymes from NF liquor starter.
To verify the feasibility of this method, enzymes related to starch degradation are selected, since starch is the main composition of wheat material in NF liquor starter . In the liquor starter, alpha-amylase makes the largest contribution to liquefaction of starch, and works efficiently with glucoamylase to produce fermentable reducing sugars [4, 8]. And thermostable α-amylases are more attractive in biotechnological processes, since they are stable over 60 °C and allow a higher operation temperature which result in higher reactivity, higher process yield, fewer contamination, and so on . NF liquor starter is a promising resource for thermostable fungal α-amylase, since its making process is subjected to high temperature (N3) of 62 °C for 8 days. Moreover, based on previous metatranscriptomics analysis of NF liquor starter, enzymes related to starch metabolism, e.g., α-amylase, β-glucosidase and glucoamylase, showed relatively high expression level at high temperature stage (N3), and α-amylases exhibited the second highest RPKM (Reads Per Kilobase per Million) value up to 465.7, which stands for the second highest expressional enzymes in N3 . Therefore, thermostable α-amylase is finally selected to be directly mined from NF liquor starter, which should have high efficiency in liquefaction of starch.
In the present study, we provided a direct and efficient way to mine enzymes from man-made environment of Chinese NF liquor starter, by which one fungal thermostable α-amylase was successfully obtained and characterized. This α-amylase was the highest expression enzymes related to starch hydrolysis at high temperature period (62 °C), and showed interesting characteristics, such as Ca2+-dependent on activity and thermostability, high stability at 60 °C, acidic pH optima at 5.0–5.5, the more efficient hydrolysis on amylopectin than on amylose, high activity on starches and tolerances of high substrates concentrations (15 mg/ml). This study would shell light on understanding the important role of this thermostable α-amylase in NF liquor starters and pave the way toward the optimization of liquor production and improvement of liquor quality. To the best of our knowledge, this is the first report of directly mining enzymes from NF liquor starter.
Escherichia coli DH5α strain (Sangon Biotech, Shanghai) was used for gene cloning and plasmid maintenance throughout the study, and Pichia pastoris X33 strain (Invitrogen, Carlsbad, CA, USA) was used for protein expression. The pGAPZαA vector (Invitrogen, Carlsbad, CA, USA) was used for gene cloning. Potato starch, wheat starch, corn starch, amylose (potato) and amylopectin (potato) were obtained from Sigma-Aldrich (St. Louis, MO). The Mix (Green) for PCR amplification was from TsingKe (Beijing, China). The QIAprep Spin Miniprep Kit and RNeasy@ Midi Kit were obtained from Qiagen (Valencia, CA). SMART® cDNA Library Construction Kit, Advantage® 2 PCR Kit and the Talon metal affinity resin were purchased from Clontech Laboratories, Inc. (Mountain View, CA). The Amicon@ ultra centrifugal filters were obtained from Millipore (Billerica, MA). All other reagents were purchased from general commercial suppliers and used without further purification.
Liquor starter sampling, RNA extraction and cDNA library construction
NF liquor starter was sampled from a liquor fermentation factory in Yibing, Sichuan, China. As described in our previous work , sample N3 was collected after 9 days of liquor starter fermentation with temperature around 62 °C. Briefly, samples were frozen in liquid nitrogen immediately after obtained in factory, transferred to 50 ml RNase free tubes and kept in dry ice. Finally, all samples were transferred to Chengdu Biology Institute, Chinese Academy of Sciences and stored at − 80 °C for further research.
A previously published protocol  was used to extract total RNA from liquor starter with some modifications. In short, 1 g of liquor starter was homogenized into fine powder in a precooled mortar. Next, 4 ml borate buffer [200 mM sodium borate (pH 9.0), 30 mM ethyleneglycoltetraacetic acid (EGTA), 1% (w/v) sodium dodecyl sulfate (SDS), 4% (w/v) polyvinylpyrrolidone (PVP), and 0.5% (v/v) Nonidet-40 (NP-40), 10 mM β-mercaptoethanol and 0.03% (v/v) RNase inhibitor] and 280 µl of proteinase K (20 mg/ml) were mixed and incubated at room temperature for 2 min. The RNA of this crude lysate was then centrifuged, precipitated with 70% ethanol, and cleaned according to the RNeasy Midi Kit protocol. An extra treatment with DNase I (Fermentas, USA) on RNA mixture was also performed according to the manufacturer’s protocol.
Three microliters of total RNA (around 1 µg) was used as template for first-strand synthesis with MMLV Reverse Transcriptase, after which the cDNAs were amplified via 20 cycles of a long distance PCR (LD-PCR) using the SMART® cDNA Library Construction Kit. The resulting environmental cDNAs were used as template to specifically amplify α-amylase gene sequence.
Gene cloning, expression and protein purification
The recombinant plasmid with correct insert (pGAPZaA/NFAmy13A) was linearized by Avr II and transformed into P. pastoris X33 using MicroPulser Electroporator (Bio-Rad Laboratories, Hercules, CA, USA) for gene expression. After 3 days incubation on YPD medium (10 g/l yeast extract, 20 g/l peptone and 20 g/l dextrose) supplemented with 1 M sorbitol and 100 μg/ml zeocin at 30 °C, single colonies were inoculated into 25 ml YPD medium with same concentrations of sorbitol and zeocin at 30 °C with vigorous shaking at 250 rpm for 2 days, and transformants with correct inserts were analyzed by PCR amplification with pGAP Forward (5′-GTCCCTATTTCAATCAATTGAA-3′) and 3′ AOX (5′-GCAAATGGCATTCTGACATCC-3′) primers according to Invitrogen protocol. The correct transformants were further verified by activity assays in supernatants after centrifugation at 6000g for 5 min at 4 °C.
The transformants with correct inserts were expressed in 500 ml YPD medium supplemented with same amount of sorbitol and zeocin at 30 °C and 250 rpm for 2 days. After centrifuge, supernatants were heated twice at 55 °C for 15 min since proteins from N3 were expected to be thermostable, and the precipitated host proteins were pelleted by centrifugation at 12,000×g for 10 min at 4 °C. Then, supernatants were filtered through 0.45 μm MF-Millipore membrane and adjusted to Tris–HCl buffer (pH 7.5, 50 mM Tris–HCl, 300 mM NaCl). The resulting supernatants were applied to the talon metal affinity resin and the recombinant proteins with N-terminal 6-Histidine-tag were purified according to the manufacturer’s instruction (Clontech). The bound proteins were eluted with the elution buffer (150 mM imidazole, 50 mM Tris–HCl, 300 mM NaCl, pH 7.5), and the fractions were analyzed by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE). The fractions containing the purified NFAmy13A proteins were concentrated, the buffer of which was changed to a protein storage buffer (50 mM Tris–HCl, 150 mM NaCl, pH 7.5) with Amicon Ultra-10 centrifugal filters. The protein concentrations were measured using a NanoDrop 2000c (Thermo Fisher Scientific Inc., Waltham, MA) and the Beer-Lambert law with the extinction coefficients of 91,010/M/cm for NFAmy13A.
Zymogram analysis and plate-based activity assay of NFAmy13A
For zymogram analysis, around 20 μg purified NFAmy13A was loaded onto 10% native-PAGE gel (without SDS). After electrophoresis, the gel was washed with 50 mM citrate buffer (pH 5.5) for three times. Then the gel was overlaid on a sheet containing 1% soluble starch with 1.5% agar and 0.01% Trypan Blue in 50 mM citrate buffer (pH 5.5) for 1 h at 60 °C. Finally, amylase activity was visualized as a clear zone by staining this sheet with Lugol’s iodine solution.
For plate-based activity assay, around 20 μg purified NFAmy13A was added onto the center hole of plate containing 0.1% AZCL-amylose (Megazyme) with 1% agarose in 50 mM citrate buffer (pH 5.5), and the plate was kept at 60 °C for 2 h. Then the amylase activity was visualized with blue zone around the hole.
The optimal pH of NFAmy13A was determined by incubating 40 nM NFAmy13A with 5 mg/ml potato starch between pH 4.0 and 9.0 (50 mM citrate buffer for pH 4.0–6.0, 50 mM sodium phosphate buffer for pH 6.0–8.0, 50 mM Tris–HCl for pH 8.0–9.0) at 55 °C for 30 min. The reducing sugars released were measured using the para-hydroxybenzoic acid hydrazide (pHBAH, Sigma-Aldrich, St. Louis, MO) assay  with glucose as the standard. Meanwhile, the optimal temperature was determined by incubation of 40 nM NFAmy13A and 5 mg/ml potato starch at its optimal pH at different temperatures ranging from 30 to 80 °C for 30 min.
The specific activity of NFAmy13A was determined by incubating 20 nM enzymes with 5 mg/ml potato starch at 60 °C and pH 5.5 for different time intervals, within the range where the slopes of released glucose equivalents versus time were linear. One unit of alpha-amylase activity was defined as the quantity of enzyme capable of releasing 1 μmol glucose equivalent per minute under its optimized conditions. The digestion of various substrates was also characterized by incubating 100 nM NFAmy13A with 5 mg/ml substrates at 60 °C and pH 5.5 for 30 min.
To determine the thermostability of NFAmy13A, enzymes (80 nM) were incubated in a citrate buffer (pH 5.5) at 50, 60 and 70 °C in THERMO SHAKER. Samples were taken out at different time points and placed on ice. The residual enzymatic activity was determined by incubating 40 nM enzymes with 5 mg/ml amylopectin at 60 °C in a citrate buffer (pH 5.5) for 30 min.
Effect of metal salts and chemical additives on amylase activity
The effect of various metal salts was studied by adding 1 and 10 mM metal salts and additives to the reaction mixture of 100 nM enzymes with 5 mg/ml amylopectin under standard assay. Relative activities were calculated as a percentage of the activity of the unadded control as 100%.
Kinetics hydrolysis of NFAmy13A on starch substrates
The kinetics studies of NFAmy13A were determined by incubating purified NFAmy13A with different concentrations of starch substrates, i.e., amylopectin, amylose, potato starch, corn starch or wheat starch, ranging from 0.1 to 18 mg/ml. The reducing ends were measured after incubation under normal condition for 30 min in the presence of 10 mM CaCl2, and the velocities were kept in a constant scope under every condition by using low concentration of 20 nM enzyme.
Application of NFAmy13A in the hydrolysis of raw potato starch substrates
To measure the effect of concentrations of starch substrates, i.e., potato starch, corn starch or wheat starch, their concentrations were varied from 1 to 18 mg/ml in citrate buffer (pH 5.5) containing high concentration of 1 μM enzymes and 10 mM CaCl2. After incubation at 60 °C for 20 h, the concentration of reducing ends was estimated using the pHBAH assay as described above. Then, the end products was analyzed by thin-layer chromatography (TLC) with glucose (M1) and maltose-oligosaccharides (M2–M6) as standards and n-butanol-acetic acid-H2O (10:5:1, vol/vol/vol) as developing mobile phase. The sugars were visualized by spraying with a 1:1 (vol/vol) mixture of methanolic orcinol (0.2% wt/vol) and sulfuric acid (20% vol/vol) followed by heating at 100 °C for 5 min .
Nucleotide sequence accession numbers
The nucleotide sequence of NFAmy13A was deposited at the GenBank database with accession number MF765801.
RNA extraction and cDNA library construction
Total RNA was extracted from 1 g of liquor starter sample N3 and approximately 15 μg RNA was obtained with high purity. Full-length cDNA was synthesized by the initial reverse transcription and enriched by subsequent LD PCR. When analyzed by agarose gel, environmental double strands cDNA appeared as a strong smear ranging from 100 bp to 4 kb, and it was adequate for the subsequent specific amplification.
Cloning, expression, and purification of NFAmy13A
ORF17588 was identified to predictively encode an alpha-amylase, which was designated as NFAmy13A since it was the first characterized alpha-amylase in NF liquor starter. Based on our previous metatranscriptomics analyses of NF liquor starter, NFAmy13A was the only alpha-amylase in the top 20 highest expression level of glycoside hydrolases in N3 (Additional file 1: Table S1) with RPKM value of 293.5, and accounted for around 63% of total alpha-amylases in N3 (Additional file 1: Table S2), thus being the highest expression level of alpha-amylases in starch degradation of N3. In addition, NFAmy13A also showed active expression with RPKM value of 30.9 in mature stage of NF liquor starter according to our previous metatranscriptomic analysis (Additional file 1: Table S2). The wheat material of NF liquor starter is rich in starch. Therefore, NFAmy13A could play a pivotal role in liquefaction of NF liquor starter at high temperature stage and mature stage, and it was characterized in present work.
The amino acid sequence of NFAmy13A was analyzed by the Pfam server (http://pfam.sanger.ac.uk/), and it had alpha-amylase domain and DUF1966 domain (Fig. 1a). The product of NFAmy13A gene had a signal peptide when predicted on SignalP 4.1 Server (http://www.cbs.dtu.dk/services/SignalP/) (Fig. 1a). The NFAmy13A gene sequence (1431 bp), without signal peptide sequence, was successfully obtained by specific amplification with primers NFAf/NFAr from ds cDNA of N3, and one colony with correct gene integration into genome of P. pastoris X33 was identified by PCR with primers pGAP Forward/3′ AOX from three colonies (Fig. 1b). This colony showed the highest activity of 28.3 U/ml when cultured for 72 h. NFAmy13A was purified to near homogeneity, and the apparent molecular masses of the purified recombinant NFAmy13A corresponded well with its calculated values (56.1 KD) (Fig. 1c). Obviously, purified NFAmy13A showed strong amylase activity in degrading starch in a native-PAGE gel (Fig. 1c) and an agarose plate (Fig. 1d), when analyzed with zymogram method and plate-based activity assays, respectively.
Characterization of NFamy13A
The hydrolysis of various substrates catalyzed by NFAmy13A
Relative activity (%)
α(1 → 4)–α(1 → 6) glucose
100.0 ± 4.9
α(1 → 4) glucose
15.5 ± 1.1
α(1 → 4)–α(1 → 6) glucose
62.6 ± 9.4
α(1 → 4)–α(1 → 6) glucose
21.8 ± 1.8
α(1 → 4)–α(1 → 6) glucose
30.7 ± 1.6
α(1 → 4) glucose
18.9 ± 1.9
White dextrin (corn)
α(1 → 4)–α(1 → 6) glucose
66.1 ± 4.8
α(1 → 6)–α(1 → 4) glucose
2.3 ± 1.5
α(1 → 6)–α(1 → 3) glucose
α(1 → 4)–α(1 → 6) glucose
11.2 ± 0.6
β(1 → 4) glucose
β(1 → 4) glucose
Effects of different metal salts and chemical additives on activity of NFAmy13A
Relative activity (%)
α-Amylase (no additives)
100.0 ± 2.5
100.0 ± 1.1
98.1 ± 1.1
147.5 ± 5.1
96.4 ± 5.0
98.9 ± 5.1
94.3 ± 3.2
90.8 ± 2.7
64.6 ± 0.8
47.5 ± 3.9
93.2 ± 1.7
81.1 ± 5.9
95.0 ± 0.6
83.9 ± 0.0
97.7 ± 0.9
95.7 ± 0.5
95.5 ± 2.8
115.8 ± 3.2
97.2 ± 0.4
90.9 ± 1.4
95.0 ± 2.6
84.2 ± 5.4
94.4 ± 2.0
92.3 ± 1.4
49.0 ± 4.4
2.2 ± 0.6
97.8 ± 0.8
87.2 ± 3.9
80.0 ± 3.7
61.7 ± 6.7
Application of NFAmy13A in the hydrolysis of starch substrates
NF liquor starter is enriched with special and stable microbial communities after several 1000 years’ evolution, and plenty of active enzymes are found with efficient capacity in degrading carbohydrates and protein. However, in a pretty long time, few active enzymes were mined and characterized from NF liquor starter by traditional culture based methods. Recently, our previous metatranscriptomic study on NF liquor starter might provide a direct and easy sequence-based method to mine those functional enzymes and understand their roles in NF liquor brewing. Among these enzymes, α-amylases play a pivotal role in the liquefaction of starch, and thermostable α-amylases gains more attentions due to their potential applications at a high operation temperature (> 60 °C) compared to mesophilic α-amylases. Therefore, this study was performed to verify the feasibility of directly mining enzymes from NF liquor starter, and a thermostable α-amylase (NFAmy13A) was successfully obtained from high temperature period (N3).
Comparison of enzymatic characteristics among NFAmy13A and previously reported fungal α-amylases
Specificity activity (U/mg)
Optimal temperature (°C)
Liquor starter (Fungus)
t1/2: 1.5 h at 60 °C, 0.4 h at 70 °C; in the presence of 0.01 M CaCl2, t1/2: 16 h at 60 °C, 0.7 h at 70 °C
Co2+, Hg2+, SDS
Aspergillus awamori KT-11
Zn2+, Cu2+, Hg2+
Aspergillus flavus var. columnaris
96% loss of activity in absence of Ca2+, 10% loss of activity in presence of 0.01 M CaCl2 after incubation at 60 °C for 10 min
t1/2: 17 min at 45 °C
Co2+, Mn2+, Fe3+
Aspergillus niger CBS 513.88
Lost rapidly at above 35 °C for 10 min
Escherichia coli BL21
Aspergillus niger JGI 24
Around 20% loss of activity after incubation at 30 °C for 50 min
t1/2: 20 min at 70 °C
Hg2+, Ag+, Fe3+
Ca2+, NH4+, Na+, K+, Mn2+, Mg2+
Aspergillus oryzae ATCC 76080
Lost 80% activity after incubation at 50 °C for 30 min
Hg2+, DNFB, NBSI
Aspergillus oryzae EMS-18
Mg2+, Mn2+, Na+, Zn2+, Ni2+, Fe2+, Cu2+, Co2+ and Ba2+
Aspergillus oryzae S2
t1/2: 60 min at 50 °C
Mg2+, Fe2+, Ba2+, Cu2+, Co2+, Mo2+, and Mn2+
t1/2: 30 min at 70 °C
Pb2+, Cu2+, Ag+, Fe3+
40% loss of activity after incubation at 50 °C for 10 min
Ni2+, EDTA, Methanol, Teween-20/80
Malbranchea cinnamomea S168 amylose
Around 50% loss of activity after incubation at 60 °C for 30 min
t1/2: 53 min at 60 °C
Cu2+, Al3+Fe3+, EDTA, K+, Pb2+, Zn2+
Ca2+, Co2+, Mn2+
20% loss of activity after incubation at 50 °C for 30 min
Cd2+, Cu2+, Hg2+, Al3+, and Zn2+
Preussia minima EL-14
50% loss of activity after incubation at 60 °C for 5 min
Independence of Ca2+
Rhizomucor pusillus GX-3
t1/2: 75 min at 60 °C
Saccharomycopsis fibuligera KZ, amylose
Around 80% loss of activity after incubation at 55 °C for 30 min
Cu2+, Mn2+, Ba2+, Fe2+
Weakly stimulated by Ca2+
t1/2: 12 min at 60 °C
Independence of Ca2+
t1/2: 2 h at 70 °C
Ag+, Ba2+, Co2+, Cu2+, EDTA, Hg2+, Mg2+, Pb2+, Zn2+
Thermobifida fusca NTU22
25% loss of activity after incubation at 60 °C for 3 h
32 and 94% loss of activity after incubation at 50 °C for 2 and 18 h
Ba2+, Ca2+, Cd2+, Mg2+, Mn2+
At 65 °C (t1/2: 0.6 h) the enzyme is nearly 8 times more stable in presence of Ca2+
t1/2: 140 min at 60 °C, 10 min at 70 °C
Talaromyces pinophilus 1–95
60% loss of activity after incubation at 55 °C for 1 h
Ag+, Cu2+, Mn2+
Co2+, Fe2+, Fe3+
Similar to most of fungal α-amylases, NFAmy13A had acidic pH optima at < 5.5 (Table 3), which is preferred in starch industries [28–30]. On the contrary, some fungal α-amylases showed high pH optima at > 7.0 [26, 31, 32], which could be used in detergent industry. As shown in Table 3, most of fungal α-amylases are unable to work at temperatures more than 50–60 °C. Meanwhile, NFAmy13A had an optimum temperature at 60 °C and was stable with half-life of 1.5 h at 60 °C. Similar or higher thermostabilities were also found in a few fungal amylases from Aspergillus niveus , Paecilomyces variotii , Rhizomucor pusillus , Streptomyces megasporus  and Thermomyces lanuginosus . Thermostable fungal α-amylases are mostly used in the starch hydrolysis of baking and brewing industries [8, 37].
Among the cation and additives tested, 10 mM Hg2+ largely inhibited NFAmy13A activity, which has been well observed on some fungal alpha-amylases [33, 35, 38–42]. The stimulation of Ca2+ was also found in other fungal alpha-amylases [22, 31–34, 43–48]. The ‘high-affinity’ Ca2+-binding sites (Asn121, Glu162, Asp175, His210) in 2GUY-A were highly conserved in NFAmy13A (Asn123, Glu164, Asp177, His212) (Fig. 6), indicating that NFAmy13A was a metalloenzyme and strongly bound Ca2+. Similar as some α-amylases reported previously [22, 30, 33, 49], NFAmy13A was insensitive to EDTA, and one of the possible reason might be that the affinity of calcium to NFAmy13A was stronger than that of EDTA. Moreover, the stabilizing effect of Ca2+ on thermostability was observed in NFAmy13A, which might be explained due to the formation of a calcium–sodium–calcium metal triad in the main Ca2+-binding site of the enzyme , and has also been found in some fungal alpha-amylases [43, 47].
As shown in Table 1 and Fig. 4, NFAmy13A showed the maximum activity on amylopectin, followed by starch, amylose, glycogen, and pullulan at all detected concentrations, and its specificity activity on amylopectin was 200.4 U/mg, which was within the range values of the reported fungal α-amylases (Table 3). In general, amylopectin has α-1,4 glycosidic bond in the main chain and α-1,6 glycosidic bond in the branching chain, resulting in many end points onto which enzymes can easily attach. Meanwhile, amylose only has α-1,4 glycosidic bond in the main chain and forms tightly packed helical structure. Possibly, their structural differences were one of the reasons that NFAmy13A was more efficient to degrade amylopectin than amylose. This preference of NFAmy13A on amylopectin further verified its important role in NF liquor starter, since wheat material of NF liquor starter has higher amylopectin content of its starch than its amylose content . Moreover, this preference of NFAmy13A potentially enhance its pivotal role in the following stage of alcohol fermentation, because the main material of alcohol fermentation is sorghum  and sorghum also has higher amylopectin content . Similar preference between amylopectin and amylose was also found in other fungus α-amylase [22, 25]. Whereas, some fungal amylases showed higher activity on amylose than on amylopectin [21, 40, 49, 53]. Similar as amylopectin, glycogen is also composed with main chain of α-1,4 glycosidic bond and side chain of α-1,6 glycosidic bond, but being more branched and compact. This might be the reason that NFAmy13A could catalyze glycogen effectively and the degradation efficiency on glycogen is lower than that on amylopectin, which was also observed in other fungal α-amylases [22, 25, 48]. In addition, NFAmy13A exhibited very low activity toward pullulan, which perhaps resulted from the resistant structure that maltotriose (α-1,4 glycosidic bond) unites are connected to each other by α-1,6 glycosidic bond in pullulan. Most other fungal α-amylases also showed weak activity toward pullulan [22, 48, 49, 53], except for fungal α-amylase from Malbranchea cinnamomea, which showed high activity on pullulan .
NFAmy13A showed high activity toward soluble starches from corn, wheat, and potato, and worked efficiently at high concentrations up to 15 mg/ml. Its end products were maltose, glucose and minor maltotriose. Among them, main products of maltose and glucose can be easily uptake by yeast in the following alcohol fermentation stage, which further verified its pivotal role in the liquor fermentation. Therefore, as shown in Table 3, compared with other fungal α-amylases, NFAmy13A showed some advantageous characteristics in hydrolyzing starch substrates, e.g., high thermostability at 60 °C, acidic pH optima at 5.0–5.5, Ca2+-dependent, high activity on wheat starch, the more efficient hydrolysis on amylopectin than on amylose, and tolerances at high substrates concentrations (15 mg/ml), which to some extent proved previous finding that NFAmy13A was the highest expressed α-amylase at 62 °C and relatively high expressed α-amylase at mature stage in NF liquor starter, thus being the largest contribution in liquefying starch into glucose and maltose at solid state at high temperature stage and mature stage . Moreover, as we know, corn and wheat, are also widely used for fuel ethanol production , and high activity toward corn and wheat highlights the potential applications of NFAmy13A in ethanol industrial. In addition, taking into account the safe advantage of fungal α-amylase, NFAmy13A was a good candidate in starch hydrolysis in food and pharmaceutical industries.
A direct and efficient sequence-based method of metatranscriptomics is provided to mine active enzymes from NF liquor starter in present work. And by this way, a thermostable fungal α-amylase (NFAmy13A) gene is successfully obtained from environmental cDNA library of NF liquor starter, and expressed in P. pastoris. The recombinant enzyme of NFAmy13A has optimal pH of 5.0–5.5 and optimal temperature as high as 60 °C. When compared with other fungal α-amylases, NFAmy13A shows interesting characteristics, such as high thermostability, Ca2+-dependent on activity and thermostability, high activity on amylopectin, starches (from corn, wheat, and potato), amylose and glycogen, the more efficient hydrolysis on amylopectin than on amylose, and tolerances of high substrates concentrations. Therefore, NFAmy13A not only plays pivotal role in the solid-state SSF of starch liquefaction in NF liquor brewing, but also has potential application in the solid-state SSF process of other food industries, and pharmaceutical industries. Successfully mining α-amylase (NFAmy13A) from NF liquor starter will stimulate the characterization of more enzymes related to polysaccharides degradation in future, such as starch, cellulose, and hemicellulose. Their synergistic roles in degrading polysaccharides in liquor starter will also be studied, thus paving the way toward the optimization of liquor production and improvement of liquor quality, and stimulating potential application as safe additive for other industrial applications, such as bioenergy production, food or feed preservation and high valued-added products.
ZY, HZ, YJ, KH, DL, HL and YF designed the experiment; ZY, DZ and HH collected liquor starter samples; ZY performed the experiment and analyzed data; ZY wrote the main manuscript; ZY, YJ and HZ revised the manuscript. All authors read and approved the final manuscript.
We thank Professors Zhongyan Wang for providing valuable suggestions concerning liquor starter research.
The authors declare that they have no competing interests.
Availability of data and materials
All the data generated or analyzed during this study have been included in this published article.
Ethics approval and consent to participate
This study does not contain any experiment with human participants or animals performed by any of the authors.
This study was supported by China Agriculture Research System (CARS-10-B22); the National Key Technology R&D Program of China (No. 2015BAD15B01); the National Natural Science for Youth Foundation of China (Nos. 31400685 and 21606218); the National Natural Science for General Foundation of China (No. 31770395); Science & Technology Program of Sichuan Province (2017NZ0018 and 2017HH0077); Key Laboratory of Environmental and Applied Microbiology, Chengdu Institute of Biology, Chinese Academy of Sciences (Nos. KLEAMCAS201501, KLCAS-2016-02 and KLCAS-2016-06).
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