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碱性木聚糖酶产生菌的筛选、XynG1-3基因克隆表达及酶学性质研究 被引量:7

Screening of Alkaline Xylanase Producing Strains and Cloning,Expression and Characterization of Xylanase Gene XynG1-3
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摘要 从造纸厂周边碱性土壤中分离、筛选到一株产碱性木聚糖酶的细菌G1-3,根据形态和生理、生化特性并结合16SrDNA序列分析,鉴定菌株G1-3为短小芽孢杆菌,命名为Bacillus pumilusG1-3。利用克隆表达载体pET-22b(+),实现了Bacillus pumilusG1-3碱性木聚糖酶基因XynG1-3在E.coliBL21中的表达。经氨基酸序列分析,木聚糖酶XynG1-3属于GH11家族的小分子木聚糖酶。重组木聚糖酶XynG1-3经镍离子亲和层析一步纯化后,获得凝胶电泳条带单一的蛋白样品,经SDS-PAGE检测其分子量为24 kD。对酶学性质进行分析,重组酶XynG1-3最适作用温度为55℃,最适作用pH为8.0;该酶在60℃保温1 h,残余酶活保持为原来的56%,pH作用范围较广,在pH10.0下保存1 h,残余酶活仍能保持75%,为耐碱性木聚糖酶。 A new alkaline xylanase-producing strain was isolated from alkaline soil around paper mill and was identified as Bacillus pumilus G1-3 based on the evidence from its physiological and biochemical characteristics and 16S rDNA sequences.The gene coding for XynG1-3 consists of 687 bp was cloned into the expression vector pET-22b and expressed in E.coli BL21(DE3).XynG1-3 was determined to be a new xylanase belonging to glycoside hydrolase family 11 based on its amino acid sequence.The recombinant xylanase was purified by Ni2+-NTA affinity chromatography.The molecular weight of the purified XynG1-3 was estimated to be 24 kD by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.It revealed optimal activity at 55℃ and pH8.0 and remained high activity over a large range of pH(6.0-10.0)which remained at least 75% residual activity at pH 10.0 for 1 h.
出处 《生物技术通报》 CAS CSCD 北大核心 2012年第10期106-113,共8页 Biotechnology Bulletin
基金 国家自然科学基金项目(31101219)
关键词 短小芽孢杆菌 碱性木聚糖酶 筛选 鉴定 克隆 表达 酶学性质 Bacillus pumilus Alkaline xylanase Screening Identification Cloning Expression Enzymic properties
作者简介 郑宏臣,男,博士研究生,研究方向:发酵工程,E-mail:hongchenzheng@yahoo.cn;通讯作者:路福平,男,教授,博士生导师,研究方向:微生物生物活性物质开发与工业微生物育种等,E-mail:lfp@tust.edu.cn
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  • 1Beg QK, Kapoor M, Mahajan L, et al. Microbial xylanases and their industrial applications : a review. Appl Microbiol Biotechnol, 2001, 56 : 326-338.
  • 2Ouyang J, Wang S, Wang Y, et al. Production of a Trichoderma reesei QM9414 xylanase in Pichia pastoris and its application in biobleaehing of wheat straw pulp. World J Mierobiol Biotechnol, 2011,27 (4) : 751-758.
  • 3Polizeli ML, Rizzatti AC, Monti R, et al. Xylanases from fungi : properties and industrial applications. Appl Microbiol Bioteehnol, 2005, 67 : 577-591.
  • 4de Ara6jo JH, de Moraes FF, Zanin GM. Bleaching of kraft pulp with commercial xylanases. Appl Bioehem Bioteehnol, 1999, 79 ( 1-3 ) : 713-722.
  • 5Sharma A, Adhikari S, Satyanarayana T. Alkali-thermostable and cellulase-free xylanase production by an extreme thermophile Geobacillus thermoleovorans. World Journal of Microbiology and Biotechnology, 2006, 23 ( 4 ) : 483-490.
  • 6Ko C, Chen W, Tsai C, et al. Paenibacillus campinasensis BL11 : A wood material-utilizing bacterial strain isolated from black liquor. Bioresource Teehnology, 2007, 98 ( 14 ) : 2727-2733.
  • 7Alves-Prado HF, Pavezzi FC, Leite RS, et al. Screening and production study of microbial xylauase producers from Brazilian Cerrado. Applied Biochemistry and Bioteehnology, 2010, 161 ( 1-8 ):333-346.
  • 8. Menon G, Mody K, Keshri J, et al. Isolation, purification, and characterization of haloalkaline xylanase from a marine Bacillus pumilus strain, GESF-1. Biotechnology and Bioprocess Engineering, 2011, 15 (6) : 998-1005.
  • 9代义,吕淑霞,林英,黄益,马丽.高产木聚糖酶菌株筛选、鉴定及产酶条件的研究[J].生物技术,2008,18(2):70-73. 被引量:8
  • 10包怡红,李雪龙.木聚糖酶产生菌——类芽孢杆菌的筛选及其酶学性质研究[J].中国食品学报,2008,8(2):36-41. 被引量:19

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