Molecular Cloning and Characterization of a Novel α-Amylase from Antarctic Sea Ice Bacterium Pseudoalteromonas sp. M175 and Its Primary Application in Detergent

A novel cold-adapted and salt-tolerant α-amylase gene (amy175) from Antarctic sea ice bacterium Pseudoalteromonas sp. M175 was successfully cloned and expressed. The open reading frame (ORF) of amy175 had 1722 bp encoding a protein of 573 amino acids residues. Multiple alignments indicated Amy175 had seven highly conserved sequences and the putative catalytic triad (Asp244, Glu286, and Asp372). It was the first identified member of GH13_36 subfamily which contained QPDLN in the CSR V. The recombinant enzyme (Amy175) was purified to homogeneity with a molecular mass of about 62 kDa on SDS-PAGE. It had a mixed enzyme specificity of α-amylase and α-glucosidase. Amy175 displayed highest activity at pH 8.0 and 25°C and exhibited extreme salt-resistance with the maximum activity at 1 M NaCl. Amy175 was strongly stimulated by Mg2+, Ni2+, K+, 1 mM Ca2+, 1 mM Ba2+, 1 mM Pb2+, 1 mM sodium dodecyl sulphate (SDS), and 10% dimethyl sulfoxide (DMSO) but was significantly inhibited by Cu2+, Mn2+, Hg2+, 10 mM β-mercaptoethanol (β-ME), and 10% Tween 80. Amy175 demonstrated excellent resistance towards all the tested commercial detergents, and wash performance analysis displayed that the addition of Amy175 improved the stain removal efficiency. This study demonstrated that Amy175 would be proposed as a novel α-amylase source for industrial application in the future.

Most -amylases belong to glycoside hydrolase family 13 (GH13). Among classification systems of glycoside hydrolases (GHs), the family GH13 forms the clan GH-H together with the families 70 and 77 [6]. The classification system of GH has been incorporated into the Carbohydrate-Active enZymes database (CAZy) [7]. As the largest GH family, the family GH13 consists of more than 30 different enzyme specificities and more than 55,500 sequences (http://www.cazy.org/GH13.html). It was officially divided into 35 subfamilies by the CAZy curators in 2006 [8]. The number of GH13 subfamilies has reached 42 currently and is still updating [9,10]. Although the overall sequences of family GH13 members own very low identity, they possess 4-7 conserved sequence regions (CSRs) and a catalytic triad (Asp, Glu, and Asp) [11,12].

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The oligo-1,6-glucosidase subfamily includes mainly oligo-1,6-glucosidase, -glucosidase, trehalose synthase, sucrose isomerase, trehalose-6-phosphate hydrolase, and dextran glucosidase, and the neopullulanase subfamily consists of cyclomaltodextrinase, maltogenic amylase, and neopullulanase [13], whereas the members of GH13 36 subfamily were reported to possess a mixture of enzyme specificity ofamylase and some others from the two above-mentioned subfamilies [12]. There were efforts to define them based on specific features in their CSRs [12]. Originally oligo-1,6glucosidase and neopullulanase subfamily were distinguished using specific sequence motif QPDLN and MPKLN in their CSR V, respectively. The subfamily GH13 36 was described with the sequence MPDLN discriminating the former two subfamilies [13]. Therefore CSR V can be used as a selection marker. The GH13 36 enzymes also possess other additional sequence features, such as an invariant tryptophan in the CSR VI and a tyrosine preceding the tripeptide "GEE" at the end of the CSR VII. Moreover, some GH13 36 members have furthermore a histidine at the end of the CSR II and a tryptophan (or other aromatic residues) in the CSR III [14]. These features can be used as reference information for subfamily assignment of GH13 36-like protein without additional biochemical characterization.
To improve the productivities of various industries, novel -amylases with extreme properties such as activity at low/high-temperatures and salt-tolerance need be continuously sought for and applied in harsh industrial processing conditions. Cold-adapted enzymes that catalyze the reaction at low temperatures but lose activities by a moderate heating are highly beneficial to industries and biotechnology and have obtained increasing attentions in recent years [15][16][17][18]. For example, cold-adapted -amylases can be added to detergents for cold washing to save the energy, reduce the wear, and protect the color of fabrics [19][20][21]. In baking processes, they can be used to shorten the dough fermentation time, quickly terminate the reaction of other enzymes, and improve the properties of the bread [19]. In addition, salt-tolerant enzymes have been widely used in detergent industry and bioremediation process. Many stains on fabrics have high salt concentration that requires salt-tolerant enzymes to remove them completely. Although several cold-adapted -amylases [22][23][24][25][26][27][28][29] or salt-tolerant -amylases [22,24,[30][31][32][33] have been found, to the best of our knowledge, very few -amylases possess both properties.
Antarctic is a unique ecosystem on earth, which is composed of a combination of extreme cold, high salt, and strong radiations. Organisms of Antarctic have evolved their specialized cold and high salt tolerant enzymes to adapt to and survive in this harsh environment. In this work, a novel -amylase-producing strain Pseudoalteromonas sp. M175 (KU726544) was isolated and identified from Antarctic ice cover. A novel -amylase gene of GH13 36 subfamily, amy175, isolated from Pseudoalteromonas sp. M175 was cloned and expressed in E. coli, and then the recombinant protein was purified and fully characterized. In addition, the primary application of Amy175 was tested as detergent additives.

Gene
Cloning and Sequence Analysis. The genomic DNA of Pseudoalteromonas sp. M175 was prepared using Bacterial DNA Extraction Kit (Sangon Biotech, China). PCR primers were designed based on the sequence of the putative -amylase gene of Pseudoalteromonas haloplanktis TAC125, whose genome sequence was released in GenBank (CR954246) by Médigue et al. [34], as follows: forward primer 5 -TGTTAATAGGCGCGGTGTC-3 and reverse primer 5 -GGAGCTGTGCGTAGTAAC-3 . PCR was performed with the following conditions: 94 ∘ C, 5 min; 30 cycles of 94 ∘ C, 45 s; 55 ∘ C, 1 min; 72 ∘ C, 1 min and finally 72 ∘ C, 10 min. The PCR product was inserted into pGM-T and sequenced (Sangon Biotech, China).

Expression and Purification of the Recombinant -Amylase.
The plasmid of pGM-amy175 was used as the template. To obtain the mature -amylase, the -amylase gene (amy175) was amplified using forward primer 5 -CGCGGATCCCCA-TCAACAAATACTAAC-3 and reverse primer 5 -CCG-CTCGAGCAGTGTGTTATTTAGTAACAAT-3 (BamH I and Xho I sites underlined, respectively). The PCR product was gel purified, digested with BamH I and Xho I, and then ligated into the vector pET-28a(+) and transformed into competent E. coli DH5 cells. The recombinant plasmid pET-amy175 was transformed into competent E. coli BL21 (DE3) for protein expression and purification.
E. coli BL21 (DE3) cells with pET-amy175 were grown overnight at 37 ∘ C in LB medium containing 100 g/mL kanamycin. Subsequently, 1 mL culture was inoculated into BioMed Research International 3 50 mL LB medium and cultured at 37 ∘ C to an optical density of 0.6 at 600 nm. Expression was induced with 0.3 mM isopropyl -D-1-thiogalactopyranoside (IPTG) at 15 ∘ C for 12 h. Cells were collected by centrifugation at 7500 rpm for 20 min at 4 ∘ C and washed twice with the sterile water before being resuspended in the buffer (20 mM Tris-HCl pH 8.0, 0.5 M NaCl, 1 mM EDTA, 1 mg/mL lysozyme). The suspended solids were lysed using ultrasonic sonicator (Scientz, China) and then centrifuged at 12000 rpm for 15 min at 4 ∘ C. The supernatant was collected and applied to Ni-NTA resin affinity chromatography according to the manufacturer's instructions. Bound proteins were eluted with buffer containing 20 mM Tris-HCl, 0.5 M NaCl, 100 mM imidazole, pH 8.0.
The purity of the recombinant -amylase was analyzed by 12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and the protein concentration was measured according to the Bradford method [35]. For zymogram study, the purified -amylase was electrophoresed by SDS-free PAGE containing 1% (w/v) soluble starch. After electrophoresis, the gel was incubated in 50 mM Tris-HCl buffer (pH 8.0) for 1 h and then stained by iodine solution until a clear band appeared. The purified recombinant protein was analyzed by tandem mass spectrometry with MALDI-TOF (Bruker Daltonics, Germany) using the parameters described by Li et al. [36].

-Amylase Activity
Assay. The amylase activity was measured principally according to the Miller method [37], using the 3,5-dinitrosalicylic acid (DNS). In brief, 500 L of 50 mM Tris-HCl buffer (pH 8.0) containing 1% (w/v) soluble starch was maintained for 5 min at the desired temperature, and then 500 L of the purified enzyme was added to the buffer. After incubation for 10 min at 25 ∘ C, the reaction was stopped by the addition of 1 mL of DNS and the mixture was boiled for 5 min. The absorbance was measured at 540 nm using a UV/visible spectrophotometer (MAPADA, China). One unit of amylase activity was defined as the amount of enzyme that released 1 mg/mL maltose equivalent to reducing sugars per minute under the assay conditions.

Effects of Temperature and pH on Enzymatic Activity and
Stability. The optimum temperature of the enzyme against the soluble starch was investigated by incubating the reaction mixture at different temperatures (0-60 ∘ C) in 50 mM Tris-HCl buffer (pH 8.0). To study the thermostability, the purified recombinant -amylase was held at 30, 40, and 50 ∘ C for different time periods and the residual activity was measured as described above.
The optimum pH of the enzyme was analyzed by incubating the reaction mixture in the range of pH 5.0-11.0 at 25 ∘ C using the following buffers (50 mM): Na 2 HPO 4 -citric acid (pH 5.0-7.0), Tris-HCl (pH 7.0-9.0), and glycine-NaOH (pH 9.0-11.0). The pH stability test was performed by incubating the enzyme in the different buffers at 25 ∘ C for 1 h. The remaining activity was measured under standard conditions as described above.

Effects of NaCl on Enzymatic Activity and Stability.
The effect of NaCl on enzyme activity was tested in the range of 0-5 M at 25 ∘ C in 50 mM This-HCl buffer (pH 8.0). The effects of NaCl on enzyme stability were studied by preincubating the enzyme in 50 mM This-HCl buffer (pH 8.0) with 1 M NaCl and without NaCl, respectively, at 25 ∘ C for 0-120 min. The remaining activity was measured under standard conditions as described above. The enzyme activity at 0 min was defined as 100%.

Effects of Metal Ions and Chemical
Reagents. The effects of different metal ions, sodium dodecyl sulphate (SDS), EDTA, dithiothreitol (DTT), -mercaptoethanol ( -ME), and urea on enzyme activity were determined at the final concentration of 1 mM and 10 mM. The effects of Tween 80, Triton X-100, and dimethyl sulfoxide (DMSO) on enzyme activity were tested at 1% and 10% concentrations. The enzyme activity was measured in 50 mM This-HCl buffer (pH 8.0) containing 1% (w/v) soluble starch at 25 ∘ C.

Determination of Kinetic Parameters.
The kinetic parameters were determined by incubating the enzyme with different concentrations of soluble starch ranging from 0.125% to 2% (w/v) in 50 mM Tris-HCl buffer (pH 8.0) under standard conditions. V max and K m values were calculated from Lineweaver-Burk plot.

Substrate Specificity and Products Analysis by Thin Layer
Chromatography (TLC). The activities on -, -, and rcyclodextrin (CD), soluble starch, glycogen, amylose, amylopectin, pullulan, and several raw starches such as potato starch, corn starch, wheat starch, and pea starch were detected using DNS method at 1% (w/v) concentration during the enzyme assay. The enzyme activity for soluble starch was defined as 100%. The activity on several oligosaccharides (maltose, maltotriose, maltotetraose, sucrose, isomaltose, trehalose, raffinose, panose, and melibiose) at 1% (w/v) concentration was determined by assaying the release of glucose at 25 ∘ C for various periods with a glucose assay kit (Sigma Diagnostics no. 510). Additionally, degradation of pnitrophenyl--D-glucopyranoside (pNPG) was evaluated by measuring the release of p-nitrophenol at 410 nm after the reaction was terminated by adding an equal volume of 1 M Na 2 CO 3 .
To analyze the end hydrolysis product, the recombinant enzyme was incubated with 1% (w/v) soluble starch, maltose, maltotriose, and maltotetraose, in 50 mM Tris-HCl buffer (pH 8.0) at 25 ∘ C for various periods and 10 L of the reaction mixtures was submitted to TLC on 0.25-mm silica gel plates (GF254, 20 cm × 20 cm). Ethyl acetate-acetic acid-methanolwater (12:3:3:2, v/v) was used as the mobile phase, and the products were detected by exposing the plate to 2.0% aniline-2.0% diphenylamine-10.0% phosphate in acetone, followed by drying at 80 ∘ C for 15 min.

Compatibility Test with Various Commercial Detergents.
To confirm the potential of the recombinant enzyme as a laundry detergent additive, its compatibility and stability against various Chinese liquid commercial detergents, such as Liby5, Walch5, OMO5, Blue Moon5, Diaopai5, Tide5, Keon5, Ariel5, and Chaoneng5, were checked. All detergents at 1% (v/v) concentration were heated at 100 ∘ C for 60 min to inactivate the endogenous enzyme prior to addition of enzyme preparation. The purified recombinant enzyme was incubated with individual detergent solution for 1 h at 25 ∘ C, respectively, and then the residual activity was determined. The reaction solution without detergents was considered as the control.

Wash Performance Analysis.
Application of the recombinant enzyme as a detergent additive was evaluated on white cotton fabrics (4×4 cm 2 ) stained with chocolate and tomato sauce. To determine stain removal efficiency, each piece of stained cloth was soaked separately in any one of the following flasks containing (a) distilled water (25 mL), (b) distilled water (20 mL) and 5 mL Tide5 detergent (1%), and (c) distilled water (20 mL) and 5 mL Tide5 detergent (1%) containing 12.6 U/mL of purified recombinant enzyme. The above flasks were kept at room temperature (25 ∘ C) for 1 h. After treatment, cloth pieces were rinsed with distilled water and dried. The wash performance of the purified enzyme was judged by visual examination.

Data Analysis.
All data are expressed as mean value ± standard errors of at least triplicate determinations. The figures were drawn using Origin 8.0 software (OriginLab Corporation, USA) and statistical difference significance was analyzed using the SPSS 16.0 (SPSS, Chicago, IL) package for Windows.

Identification of Strain M175.
Strain M175, the -amylase producing strain, isolated from Antarctic sea ice is aerobic, Gram-negative. It forms smooth and bright yellow colonies on nutrient medium. Growth occurs at 0 ∘ C-40 ∘ C (optimal temperature, 15 ∘ C) and pH 3.0-11.0 (optimal pH, 8.0). NaCl is not essential for growth, but growth is enhanced in the presence of NaCl (optimal NaCl, 6%, tolerated up to 12%). It is positive for catalase, indol production, gelatin hydrolysis, and Voges-Proskaeur (VP) test. However, Methyl-Red (MR) test and nitrate reduction are all negative. The result of Oxidation/Fermentation (O/F) Test is oxidation. It can utilize the following substrates as carbon sources: D-glucose, Dlactose, D-maltose, D-xylose, sucrose, and starch ( Table 1).
The 16S rDNA analysis indicated that it was closely related to the genus Pseudoalteromonas with the highest levels of similarity (99%) to Pseudoalteromonas distincta KMM 638 T (AF082564), Pseudoalteromonas elyakovii KMM 162 T (AF082562), and Pseudoalteromonas paragorgicola KMM 3548 T (AY040229) (Figure 1). Based on the results including physiological, biochemical, and 16S rDNA alignment analyses, the strain was identified to be a member of Pseudoalteromonas, as Pseudoalteromonas sp. M175. The sequence has been submitted in GenBank with accession number KU726544.  tryptophan in the CSR VI and a tyrosine preceding the tripeptide "GEE" in its CSR VII. The tyrosine also often existed in the neopullulanase subfamily members [13]. But there was a phenylalanine rather than a histidine at the end of the CSR II, and a glycine not an aromatic residue in the CSR III. To analyze the evolutionary relationships of Amy175, 27 amylolytic enzymes that have already been biochemically characterized from these three subfamilies were selected and phylogenic tree was generated based on the neighbor-joining method by MEGA 6.0 software ( Figure 3). The result revealed that Amy175 showed a closer relationship with GH13 36 members.

Expression and
Purification of Amy175. The amy175 gene was successfully expressed in E. coli BL21 (DE3) as a Histagged fusion protein (Figure 4(a)). A clear target band was found in the induced cells (lane 5), but not in the noninduced cells (lane 2) by SDS-PAGE analysis. The purified recombinant enzyme using Ni-NTA affinity chromatography showed a single band (lane 3) with approximate molecular mass of 62 kDa and the recombinant protein was confirmed by native-PAGE with -amylase activity staining (lane 1). The enzyme was purified with the protein concentration of 385.1 g/mL and a specific activity of 337.9 U/mg that was higher than that of -amylases, e.g., Pseudoalteromonas arctica GS230 (25.5 U/mg) [23], Zunongwangia profunda (270.6 U/mg) [24], and Pseudoalteromonas sp. MY-1 (44.4 U/mg) [27], but lower than that of -amylase from Geomyces pannorum (9.72×10 3 U/mg) [38]. Additionally, the purified enzyme obtained on SDS-PAGE was excised and was submitted for MALDI-TOF-MS analysis. The peptide mass fingerprint (Figure 4(b)) was matched with the available bacteria database and revealed significant matches against -amylases from Pseudoalteromonas nigrifaciens KMM661 and Pseudoalteromonas haloplanktis TAC125 with scores of 186 and 131, respectively.

The Effects of Temperature and pH on Enzymatic Activity
and Stability. The influence of temperature on the activity of Amy175 was measured in the range of 0-60 ∘ C ( Figure 5(a)). The result showed that Amy175 exhibited high activity at low temperature with maximum activity observed at 25 ∘ C and retained about 53.2% activity at 0 ∘ C, but its activity decreased sharply above 50 ∘ C. According to temperaturestability profile depicted in Figure 5(b), Amy175 was highly stable at 30 ∘ C and could keep about 88.6% activity after 60 min incubation, whereas at 40 ∘ C and 50 ∘ C it showed poor stability, losing about 35.5% and 72.3% activity, respectively, after 10 min incubation.
25 ∘ C, while the activity sharply decreased after preincubated at pH 10.0.

The Effects of NaCl Concentration on Enzyme Activity and
Stability. The effect of NaCl on the activity of Amy175 was analyzed in the range of 0-5 M (Figure 6(a)). The enzyme exhibited the highest activity in the presence of 1 M NaCl, showing 127.5% of original activity without NaCl. It could display 87.7% of original activity even at 5 M NaCl, suggesting that Amy175 was halotolerant. In addition, the stability of enzyme was detected under the presence of 0 M and 1 M NaCl for 2 h. As shown in Figure 6(b), the presence of NaCl could improve the stability of Amy175. The activity of Amy175 was rapidly lost when preincubated without NaCl at 40 ∘ C for 120 min. However, the residual activity was increased to 82.7% and 76.7%, respectively, after preincubated with 1 M NaCl for 60 min and 120 min.

The Effects of Metal Ions and Chemical Reagents on Enzymatic
Activity. Of metal ions tested (  (Table 3). -ME (10 mM) and Tween 80 (10%) strongly inhibited the enzyme activity by 31.9% and 48.4%, while DMSO (10%) and SDS (1 mM) increased the activity by 141.9% and 118.8%, and the enzyme activities were retained more than 69.0% in the presence of EDTA, DTT, Urea, and Triton X-100 at both tested concentrations.

Kinetics Parameters.
Kinetic studies of Amy175 were determined under standard conditions using different concentrations of soluble starch (0.125%-2%) as substrate. As obtained from the Lineweaver-Burk plot, the K m and V max values were 2.53 mg/mL and 0.125 mg/mL/min, respectively. The K m value for Amy175 was lower than that of the -amylases from Pseudoalteromonas arctica GS230 (7.28 mg/mL) [23] and Zunongwangia profunda (2.74 mg/mL) [24], but higher than that of -amylase from Exiguobacterium sp. SH3 (2.29 mg/mL) [25].

Analysis of Substrate Specificity and Hydrolysis Products.
Substrate specificity of -amylase varies with the source of microorganism [39]. In Figure 7, Amy175 displayed the highest specificity towards amylose (131.4%), which is a linear glucose polymer connected by -1,4 glycosidic bonds, followed by soluble starch (100%), while amylopectin (78.7%) and glycogen (29.7%) had much lower rate of hydrolysis due to more branches connected by -1,6 glycosidic bonds  in them. Moreover, Amy175 could not hydrolyze pullulan, -, -, and r-CD. Therefore, it is suggested that Amy175 prefers -(1,4) linkage cleaving. Amy175 displayed the highest rate of hydrolysis towards pea starch (92.8%), followed by potato starch (82.1%), wheat starch (68.3%), and corn starch (53.1%). Amy175 showed different hydrolysis abilities towards various starches, due to the difference in particle size and shape, the ratio of amylose and amylopectin, and structure of the amylose and amylopectin molecules [40]. The result of oligosaccharides hydrolysis showed that the enzyme could not degrade other oligosaccharides except maltooligosaccharides and no glucose was observed even after incubation for 48 h. In addition, the enzyme was not able to hydrolyze pNPG. It is further indicated that the enzyme only cleaved -(1,4) linkage.
The hydrolysis products of soluble starch analyzed by TLC for various periods were shown in Figure 8(a). At the early stage of hydrolysis, soluble starch was hydrolyzed into maltose (G2), maltotriose (G3), maltotetraose (G4), and a small amount of higher molecular weight oligosaccharides. As the reaction proceeded, glucose (G1) gradually increased; however, G2 was still the main hydrolysis product after incubation for 48 h. These hydrolysis patterns suggest that Amy175 mainly cleave -1,4-glycosidic linkage in the interior of the starch, having great demands in the food and starch industry, such as bio-ethanol production and baking industry.
To determine whether Amy175 could perform transglycosylation, the hydrolysis products of maltooligosaccharides were analyzed by TLC (Figure 8(b)). Amy175 released a small amount of glucose from maltose at 1 h. When maltotriose and maltotetraose were degraded, Amy175 also produced oligosaccharides that were one-glucose unit smaller than the substrates. It is noteworthy that the oligosaccharides that were larger than the original substrates were produced by Amy175, especially when maltotriose was hydrolyzed for 1 h. The results suggested that Amy175 possessed transglycosylation activity.

Detergency Characteristics.
To confirm the application of Amy175 in detergent formulations, its stability was investigated in presence of various commercial detergents (Figure 9). The result revealed that Amy175 exhibited extreme stability with all the tested commercial laundry detergents and more than 76.9% residual amylase activity was retained.
Chaoneng5 was most compatible, since after 1 h of incubation at 25 ∘ C, 99.3% of its initial activity remained. of Amy175 (with 12.6 U/mL of activity) improved the stain removal efficiency. This result indicated that Amy175 could be employed as potential laundry detergent additive.

Discussion
In this study, a novel cold-adapted, salt-tolerant, and detergent-stable -amylase gene (amy175) from Antarctic sea ice bacterium Pseudoalteromonas sp. M175 was cloned, expressed, and characterized.
Amy175 had seven highly conserved regions and the putative catalytic triad. It contained QPDLN in the CSR V features for oligo-1,6-glucosidase subfamily. Although CSR V was often used as a selection marker, CSR V alone could not be enough to identify a GH13 protein's subfamily. Several GH13 amylolytic enzymes and proteins with MPDLN were assigned to the oligo-1,6-glucosidase subfamily, such as the proteins from Lactobacillus sakei (UniProt: Q38WC9), Grosmannia clavigera (UniProt: F0XH23), and Sordaria macrospora (UniProt: D1ZB31) [14]. Furthermore, the mammalian amino acid transporter also contained the oligo-1,6-glucosidasetype of QPDLN [12]. Of course, no QPDLN-containing proteins have been assigned to the GH13 36 subfamily so far. Amy175 behaved like the member of the GH13 36 subfamily in the CSR VI and CSR VII. However, unlike most GH13 36 members, it did not have a histidine at the end of the CSR II, which was similar to the intermediary GH13 36amylase from Bacillus clarkii (UniProt: B9A1J7). Moreover, it did not contain an aromatic residue in the CSR III, and several GH13 36 enzymes from Xanthomonas campestris (UniProt: Q60102), Thermotoga maritima (UniProt: P96107), and uncultured bacterium (UniProt: Q6TXT5) also had similar characteristics. The evolutionary relationships among 27 amylolytic enzymes from GH13 family showed that Amy175 possessed a closer relationship with GH13 36 subfamily.
For most GH13 36 members, the intermediary GH13 36 -amylase AmyA (PDB: 1WZA) from Halothermothrix orenii [40] was recognized as the best template, while the best templates for a few GH13 36 members were also identified from oligo-1,6-glucosidase subfamily [14]. The best structural template of Amy175 for homology modeling showed by SWISS-MODEL was a trehalose synthase (PDB: 5H2T) from the oligo-1,6-glucosidase subfamily. Its coverage value (0.87) was higher than AmyA with coverage value of 0.74. However, its sequence identity with Amy175 was only 31.59, lower than 41.37 of AmyA. On the other hand, this trehalose synthase was described as a homotetramer, while the result of native-PAGE indicated that Amy175 should be a monomer. Therefore, -amylase AmyA was more suitable as the template, and Amy175 was similar to GH13 36 -amylase structurally. The result that Amy175 degraded the soluble starch to several maltooligosaccharides suggests that Amy175 mainly hydrolyze starch internally (Figure 8(a)). It could not hydrolyze pNPG and other oligosaccharides except maltooligosaccharides, which demonstrated Amy175 could not cleave -1,6-, -1,1, and -1,2 bond, but could catalyze the hydrolysis of terminal -1,4-glucosidic linkages. Moreover, Amy175 possessed transglycosylation activity. These hydrolysis patterns suggest that Amy175 have not onlyamylase activity, but also -glucosidase activity from oligo-1,6-glucosidase subfamily. Thus, Amy175 should be a novel member of -amylase GH13 36 subfamily, which often possess a mixed enzyme specificity of -amylase, oligo-1,6glucosidase subfamily, and neopullulanase subfamily [12].
To date, several cold-adapted -amylases which have been cloned and expressed were listed in Table 4. Amy175 showed lower optimal temperature (25 ∘ C) than other coldadapted -amylases, with exceptions of AHA (25 ∘ C) from the psychrophilic bacterium Alteromonas haloplanktis and Amy 13 6 (10-15 ∘ C) from a metagenomic library. Furthermore, Amy175 could still keep 53.2% maximum activity at 0 ∘ C, while the activities retained at 0 ∘ C by AmyZ from Zunongwangia profunda [24], ParAmy from Pseudoalteromonas arctica GS230 [23], and AHA from Alteromonas haloplanktis [22] were 39.0%, 34.5%, and 20.0%, respectively. However, the  The compositions of arginine and lysine in -amylases were obtained from Genbank. The amino acid compositions of -amylases were obtained from Genbank. activity of Amy175 decreased sharply above 50 ∘ C and only about 64.5% and 27.7% activity were retained, respectively, after 10 min incubation at 40 ∘ C and 50 ∘ C, indicating relatively low thermostability, which is the typical characteristic of cold-adapted enzymes and makes inactivating the enzyme in special applications more easy and rapid [41]. Cold-adapted enzymes can carry out their functions at very low temperature because of their flexible structures [22]. Cold-adapted enzymes usually possess less arginine residues or a lower arginine/(arginine and lysine) ratio than the mesophilic and thermophilic enzymes [42]. Arginine is famous as a stabilizing residue and can reduce the flexibility by forming hydrogen bands and salt bridges with the guanidinium group [42,43]. Analysis of the amino acid sequence showed that Amy175 has less arginine residues and a lower arginine/(arginine and lysine) ratio than some other coldactive, mesophilic, or thermophilic -amylases, which may partly explain its cold activity (Table 5).
Another noticeable characteristic of Amy175 was its salttolerance. Amy175 exhibited the activity in a wide range of 0-5 M NaCl with the highest activity in the presence of 1 M NaCl (127.5% of original activity) and 87.7% activity was retained even at 5 M NaCl (Figure 6(a)). However, Amy175 is a salt-tolerant enzyme, but not a halophilic enzyme, because halophilic enzymes would be unstable and rapidly lose the activities in the absence of the salt [46], such as the halophilic -amylases produced by Marinobacter sp. EMB8 [30] and Halorubrum xinjiangense [31]. In addition, the stability of Amy175 could be dramatically improved by NaCl (Figure 6(b)), which was similar to that of theamylases from marine bacterium Zunongwangia profunda [24,32] and halophile bacterium Halothermothrix orenii [33]. Some researches showed that the hydrophobic interactions of enzyme core structures were possibly enhanced by saltingout effect under high salinity and made enzymes more compact and stable [26], which might be helpful to enhance the stability of these enzymes.
Halophilic and salt-tolerant -amylases have more acidic amino acids residues (Asp and Glu) than basic amino acids residues (Lys and Arg) [47]. An abundance of acidic amino acids produces a negative surface potential, promoting the formation of the hydrated salt ions network that reduces the tendency of aggregation and keeps the enzyme activity and stability under high salinity [48][49][50]. The proportion of acidic amino acid excess of Amy175 is 5.0%, which was higher than that of AHA (4.2%) from Alteromonas haloplanktis and Amy13A (4.8%) isolated from a pilot-plant biogas reactor, but lower than that of AmyZ (5.7%) from Zunongwangia profunda, AmyH (10.4%) from the halophilic archaeon Haloarcula hispanica, and -amylase A (18.9%) from the archaebacterium Natronococcus sp. strain Ah-36 (Table 6). In addition, Amy175 was predicted to be an extracellular enzyme with N-terminal signal peptide of 23 amino acids. Qin et al. [24] found that the extracellular proteins were more salttolerant than intracellular proteins by studying the proteins from Zunongwangia profunda.
Nies reported that Hg 2+ could bind to thiol groups in the -amylase structure to reduce its activity [57]. Amy175 was also inhibited by -ME (10 mM) and Tween 80 (10%). In contrast, the -amylase of Arthrobacter agilis PAMC 27388 was enhanced by -ME [58]. Interestingly, DMSO (10%) and SDS (1 mM) increased the activity of Amy175. The enzyme resistance towards SDS is a good characteristic, particularly in detergent industry, and SDS-stable amylases have been rarely reported [59]. Furthermore, Amy175 exhibited the tolerance to other chemical reagents and could keep more than 69.0% of the original activity. Despite loss of activity of the most -amylases with EDTA [60,61], Amy175 had completely retained its original activity with 1 mM EDTA and kept 88.9% of its original activity even with 10 mM EDTA, which was similar to the result on Bacillus KSM-K38 -amylase [62]. In addition, the activity of the -amylase from Bacillus licheniformis AT70 increased about 145% in the presence of EDTA [56]. Arikan reported that some alkaline amylases were unaffected by chelator EDTA [63]. It is probable that some metal ions can activate Amy175, but they are not essential for the catalytic reaction process.
Amy175 demonstrated not only good tolerance towards some chemical reagents, but also excellent stability against all the tested commercial detergents. In contrast, theamylase from marine Streptomyces sp. D1 retained only 35-70% of its original activity in the presence of commercial detergents [64]. Some components of commercial detergents, for example, anionic surfactants, water softening builders, and stabilizers, may have inhibitory effect on the -amylase activity, while some other ingredients such as ethoxylated surfactants and nonionic copolymeric builders may stimulate the -amylase activity [65]. Therefore, the residual amylase activity is the result of combining effects of different ingredients in the detergents.
Furthermore, the addition of Amy175 led to better stain removal from cotton fabrics than that of detergent and water alone. The amylases can help to enhance wash performance by effectively breaking down starch rich stains, protect the environment due to the biodegradability of enzymes, and make laundry detergent more sustainable [20]. All above results suggested that Amy175 could be added to laundry detergent formulations, for enhancing the ability of detergents to clean clothes in cold water.

Conclusion
In summary, a novel -amylase-producing strain Pseudoalteromonas sp. M175 (KU726544) was isolated from Antarctic ice cover and identified by physiological, biochemical, and 16S rDNA alignment analyses. A novel -amylase, Amy175, from Pseudoalteromonas sp. M175, was expressed and purified. To our knowledge, it was the first identified member of GH13 36 subfamily containing QPDLN in CSR V. It was found to have a mixed enzyme specificity of -amylase and -glucosidase and possess several remarkable extremecondition tolerance characteristics: cold-active, salt-tolerant, and relatively stable in various detergents. Such distinctive characteristics suggest that this enzyme has potential industrial applications in which low temperature-processing is required, and/or the high concentration of salts is present, and/or the residue solvents remained from prior treatments. With the global trend of using low temperature processing to save energy, cold-active amylases such as Amy175 would be a promising enzyme candidate to be used for industries such as food, detergent, and textile.

Data Availability
The data used to support the findings of this study are available from the corresponding author upon request.