Novel α- L -Arabinofuranosidase from Cellulomonas fimi ATCC 484 and Its Substrate-Specificity Analysis with the Aid of Computer

  • Ying Yang
  • , Lujia Zhang
  • , Mingrong Guo
  • , Jiaqi Sun
  • , Shingo Matsukawa
  • , Jingli Xie*
  • , Dongzhi Wei
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)3725-3733
Number of pages9
JournalJournal of Agricultural and Food Chemistry
Volume63
Issue number14
DOIs
StatePublished - 15 Apr 2015
Externally publishedYes

Keywords

  • binding energy
  • docking
  • substrate specificity
  • α-L-arabinofuranosidase

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