TY - JOUR
T1 - Novel α- L -Arabinofuranosidase from Cellulomonas fimi ATCC 484 and Its Substrate-Specificity Analysis with the Aid of Computer
AU - Yang, Ying
AU - Zhang, Lujia
AU - Guo, Mingrong
AU - Sun, Jiaqi
AU - Matsukawa, Shingo
AU - Xie, Jingli
AU - Wei, Dongzhi
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/4/15
Y1 - 2015/4/15
N2 - In the process of gene mining for novel α-l-arabinofuranosidases (AFs), the gene Celf-3321 from Cellulomonas fimi ATCC 484 encodes an AF, termed as AbfCelf, with potent activity, 19.4 U/mg under the optimum condition, pH 6.0 and 40 C. AbfCelf can hydrolyze α-1,5-linked oligosaccharides, sugar beet arabinan, linear 1,5-α-arabinan, and wheat flour arabinoxylan, which is partly different from some previously well-characterized GH 51 AFs. The traditional substrate-specificity analysis for AFs is labor-consuming and money costing, because the substrates include over 30 kinds of various 4-nitrophenol (PNP)-glycosides, oligosaccharides, and polysaccharides. Hence, a preliminary structure and mechanism based method was applied for substrate-specificity analysis. The binding energy (ΔG, kcal/mol) obtained by docking suggested the reaction possibility and coincided with the experimental results. AbfA crystal 1QW9 was used to test the rationality of docking method in simulating the interaction between enzyme and substrate, as well the credibility of the substrate-specificity analysis method in silico.
AB - In the process of gene mining for novel α-l-arabinofuranosidases (AFs), the gene Celf-3321 from Cellulomonas fimi ATCC 484 encodes an AF, termed as AbfCelf, with potent activity, 19.4 U/mg under the optimum condition, pH 6.0 and 40 C. AbfCelf can hydrolyze α-1,5-linked oligosaccharides, sugar beet arabinan, linear 1,5-α-arabinan, and wheat flour arabinoxylan, which is partly different from some previously well-characterized GH 51 AFs. The traditional substrate-specificity analysis for AFs is labor-consuming and money costing, because the substrates include over 30 kinds of various 4-nitrophenol (PNP)-glycosides, oligosaccharides, and polysaccharides. Hence, a preliminary structure and mechanism based method was applied for substrate-specificity analysis. The binding energy (ΔG, kcal/mol) obtained by docking suggested the reaction possibility and coincided with the experimental results. AbfA crystal 1QW9 was used to test the rationality of docking method in simulating the interaction between enzyme and substrate, as well the credibility of the substrate-specificity analysis method in silico.
KW - binding energy
KW - docking
KW - substrate specificity
KW - α-L-arabinofuranosidase
UR - https://www.scopus.com/pages/publications/84927918010
U2 - 10.1021/jf5059683
DO - 10.1021/jf5059683
M3 - 文章
C2 - 25797391
AN - SCOPUS:84927918010
SN - 0021-8561
VL - 63
SP - 3725
EP - 3733
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 14
ER -