Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology
研究报告     
Cloning chitinase gene of the entomopathogene fungus Metarhizium anisopliae HN1 and high-level expression in Escherichia . coli
Download: HTML   PDF(0KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  Chitinases genes from Metarhizium anisopliae which is an important entomopathogenic fungus were considered one of the key factors to invade their hosts. One Metarhizium anisopliae HN1 strain was isolated and screened by our lab. A chitinase gene was amplified by RT-PCR from Metarhizium anisopliae HN1, The whole length of this gene was 1275bp,and the nucleotide sequence of the gene was 96% similarity to that of the M. anisopliae E6 accessed in GenBank(AF02749).The gene has been registered in GenBank and its accession number is DQ011865.The gene was subcloned into prokaryon expression vector pET-22b(+),transformed this recombinant expression plasmid into E. coli strain BL 21 and effective expressed. The SDS-PAGE analysis indicated that the recombinant protein was 42kDa which is same to the reported article.The expression level of recombinant protein was about 63.3% of whole expressed proteins ,And when recombinant E.coli were crushed by freeze and supersonic wave , the activity assay indicates that the chitinase expressed in bacteria possesses biological activity.

Key wordsE. coli      Metarhizium anisopliae ,chitinase gene     
Received: 24 February 2006      Published: 25 July 2006
Cite this article:

. Cloning chitinase gene of the entomopathogene fungus Metarhizium anisopliae HN1 and high-level expression in Escherichia . coli. China Biotechnology, 2006, 26(07): 31-36.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2006/V26/I07/31

[1] WU Hong-xuan, YANG Jin-hua, SHEN Pei-jie, LI Qing-chen, HUANG Jian-zhong, QI Feng. Study on the Production of Indole-3-acetic Acid Using E. coli Cell Factory[J]. China Biotechnology, 2021, 41(1): 12-19.
[2] YAN Wei-huan,HUANG Tong,HONG Jie-fang,MA Yuan-yuan. Recent Advances in Butanol Biosynthesis of Escherichia coli[J]. China Biotechnology, 2020, 40(9): 69-76.
[3] Cheng-cheng ZHAO,Chang-po SUN,Xiao-jiao CHANG,Song-ling WU,Zhen-quan LIN. Construction and Application of Cell Lysis Systems in the Expression of Mycotoxin Degrading Enzyme in Escherichia coli[J]. China Biotechnology, 2019, 39(4): 69-77.
[4] HAN Hui-ming, LI Yong-mei. Secretory Expression of Nattokinase from Bacillus natto in Escherichia coli[J]. China Biotechnology, 2014, 34(10): 49-54.
[5] GENG Men-tin, YAO Yuan, HU Xin-wen, GUO Jian-chun, MIN Yi. Isolation of Cassava ftsZ Plastid Division Family Genes and Preliminary Identification Their Functions in E. coli[J]. China Biotechnology, 2013, 33(6): 24-29.
[6] HE Jie, SU Ling-qia, WU Jing. Optimization of Fermentation in Shake Flasks for the Xylanase in Recombinant E. coli[J]. China Biotechnology, 2013, 33(2): 41-46.
[7] XU Yi-gang, LI Dan-dan, LIU Zhong-mei, CUI Li-chun, LI Su-long. Development and Application of DPO-PCR Detection method for Enterotoxigenic E.coli[J]. China Biotechnology, 2013, 33(11): 75-80.
[8] JI Li-ping, WU Dan, WU Jing, CHEN Jian. Optimization of Fermentation in Shake Flasks for Recombinant γ-CGTase Expression in E. coli[J]. China Biotechnology, 2011, 31(10): 50-56.
[9] HUANG Jing, SHI Jian-ming, HUO Wen-ting, XU Qing-yang, XIE Xi-xian, WEN Ting-yi, CHEN Ning. The Effects of NH4+ on L-tryptophan Fermentation[J]. China Biotechnology, 2011, 31(03): 55-60.
[10] ZHANG Shu, WANG Min, HAN Mei-Lin, MA Rong-Cai, CHEN Jiang, GAO Dun-Lian. Optimization of Fermentation and Induction Conditions of Recombinant E.coli BL21(DE3)/pET30a(+)hrpNEcc[J]. China Biotechnology, 2009, 29(10): 44-49.
[11] Jian Chen . Strategies for high-level expression of recombinant protein in Escherichia coli[J]. China Biotechnology, 2007, 27(9): 103-109.