[1]向亚萍,罗楚平,周华飞,等.枯草芽孢杆菌分泌表达极耐热木聚糖酶及其酶学性质[J].江苏农业学报,2016,(05):1037-1042.[doi:10.3969/j.issn.1000-4440.2016.05.013]
　XIANG Ya-ping,LUO Chu-ping,ZHOU Hua-fei,et al.Expression of xylanse B gene of Thermotoga maritima in Bacillus subtilis and the properties of recombinase[J].,2016,(05):1037-1042.[doi:10.3969/j.issn.1000-4440.2016.05.013]
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枯草芽孢杆菌分泌表达极耐热木聚糖酶及其酶学性质()
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江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2016年05期
页码:
1037-1042
栏目:
植物保护
出版日期:
2016-11-22

文章信息/Info

Title:
Expression of xylanse B gene of Thermotoga maritima in Bacillus subtilis and the properties of recombinase
作者:
向亚萍12; 罗楚平3; 周华飞12; 刘永锋2; 陈志谊12
1. 江苏省农业科学院植物保护研究所 江苏南京210014；2. 南京农业大学植物保护学院 江苏南京210095；3. 淮阴工学院生化学院 江苏淮安223001
Author(s):
XIANG Ya-ping12; LUO Chu-ping3; ZHOU Hua-fei 12; LIU Yong-feng 1; CHEN Zhi-yi 12
1.Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China；2. College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, China；3. College of Chemical Technology, Huaiyin Institute of Technology, Huai’an 223001, China
关键词:
重组枯草芽孢杆菌; 海栖热袍菌; 极耐热木聚糖酶; 基因融合; 分泌表达
Keywords:
recombinant Bacillus subtilis; Thermotoga maritima; thermostable xylanase; gene fusion; secretory expression
分类号:
S936
DOI:
10.3969/j.issn.1000-4440.2016.05.013
文献标志码:
A
摘要:
为将海栖热袍菌极耐热木聚糖酶基因xynB（GenBank 登录号AY340789）在枯草芽孢杆菌Bs916中进行异源分泌表达，并阐明工程菌分泌重组木聚糖酶的酶学性质。克隆极耐热木聚糖酶基因xynB，将其与罗克霉素启动子融合，构建融合质粒载体pXYNB2，将其转化到枯草芽孢杆菌Bs916中，获得重组枯草芽孢杆菌(Bs916/pXYNB2)，并对重组芽孢杆菌分泌表达的极耐热木聚糖酶的酶学性质进行了研究。SDS-PAGE法测定重组枯草芽孢杆菌分泌的蛋白在相对分子质量 43 000处有明显的蛋白表达条带。重组木聚糖酶的最适反应pH值为5.0～ 5.8，重组木聚糖酶的最适反应温度大于或等于100 ℃，重组极耐热木聚糖酶在pH值4.6～7.8比较稳定，重组木聚糖酶的温度稳定性在90 ℃下保温2 h 后残存酶活83%。可见，生防枯草芽孢杆菌Bs916能有效分泌表达极耐热木聚糖酶，为以后构建多种纤维素和半纤维素在其中的协同表达，拓宽其碳源利用范围奠定基础。
Abstract:
To heterogeneously express the gene xynB encoding extremely thermostable xylanase from Thermotoga maritima in Bacillus subtilis916(Bs916) and characterize the properties of recombinant enzymes, the xynB gene with the promoter of a novel gene cluster for locillomycin were fused and resulted in a recombinant expression plasmid pXYNB2 which was then transformed into Bs916 and achieved the genetically engineered strain B. subtilis(Bs916/pXYNB2). SDS-PAGE revealed a protein with 43 000 molecular mass yielded by Bs916/pXYNB2, and the protein showed thermostable xylanase activity. The recombinant xylanase exerted activity at pH 5.0-5.8 above 100 ℃, and kept 84% of its activity after incubated at 90 ℃ for 2 h. The strain B. subtilis 916 is able to heterologouly express xynB, which lays a foundation for co-expressing cellulose and semi-cellulose.

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备注/Memo

备注/Memo:
收稿日期：2016-02-26 基金项目：国家自然科学基金项目（31570061）；国家“863”计划项目（2011AA10A201）；江苏省农业科技自主创新基金项目[CX(12)5001] 作者简介：向亚萍(1990-)，女，湖北钟祥人，硕士研究生，主要从事枯草芽孢杆菌生物防治研究。(E-mail)xiangyaping393@163.com 通讯作者：陈志谊， (Tel)025-84390393;(E-mail) chzy84390393@163.com
更新日期/Last Update: 2016-11-22