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酒酒球菌β-葡萄糖苷酶基因克隆及生物信息学分析

杨世玲 刘叶 薛楚然 王玲 何玲 刘树文

中国食品学报2017,Vol.17Issue(7):199-207,9.
中国食品学报2017,Vol.17Issue(7):199-207,9.DOI:10.16429/j.1009-7848.2017.07.025

酒酒球菌β-葡萄糖苷酶基因克隆及生物信息学分析

Cloning and Bioinformatic Analysis of the β-glucosidase Gene in Oenococcus oeni

杨世玲 1刘叶 1薛楚然 1王玲 1何玲 2刘树文1

作者信息

  • 1. 西北农林科技大学葡萄酒学院 陕西杨凌712100
  • 2. 西北农林科技大学园艺学院 陕西杨凌712100
  • 折叠

摘要

Abstract

[Objective]The aim of the work is to reveal the construction features ofβ3-glucosidase gene (bgl) in Oenococcus oeni in the molecular level and to provide a theoretical direction for further exploring the β-glucosides metabolism in O.oeni cells.[Methods] The target gene was cloned by PCR from the genomic DNA of four O.oeni strains (SD-ld,SD-2gf,31-DH and NM-2c),and the encoded productions were analyzed by bioinformatics technology.[Results] The results showed that the bgl gene has a completely open reading frame,being 2215 bp and encoding 737 amino acids.The initiation codon is TTG and the termination codon is TAA.Bioinformatic analysis indicated that the encoded protein was of weak hydrophobicity,no signal peptide and transmembrane helice,stabilization and heat-resistance,belonging to the superfamily of Glyco_hydro_3.[Conclusion] The encoded productions of bgl gene were a protein of 81625.3 u and showed BGL activity.It was considered to be non-secretory cytoplasmic protein and located in cytoplasm.

关键词

酒酒球菌/β-葡萄糖苷酶/基因克隆/生物信息学分析

Key words

Oenococcus oeni/β-glucosidase/gene cloning/bioinformatics technology

引用本文复制引用

杨世玲,刘叶,薛楚然,王玲,何玲,刘树文..酒酒球菌β-葡萄糖苷酶基因克隆及生物信息学分析[J].中国食品学报,2017,17(7):199-207,9.

基金项目

国家重点研发计划项目(2016YFD0400504) (2016YFD0400504)

国家现代农业产业技术体系建设专项(nycytx-30-ch-03) (nycytx-30-ch-03)

中国食品学报

OA北大核心CSCDCSTPCD

1009-7848

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