枯草芽孢杆菌
木聚糖酶
纤维素酶
生物
基因
质粒
生物化学
微生物学
DNA
杆菌科
葡聚糖酶
酶
遗传学
细菌
作者
M. Wolf,A. Geczi,O. Simon,Rainer Borriss
出处
期刊:Microbiology
[Microbiology Society]
日期:1995-02-01
卷期号:141 (2): 281-290
被引量:75
标识
DOI:10.1099/13500872-141-2-281
摘要
SUMMARY: The gene encoding extracellular xylanase (xynA) was amplified as a 770 bp DNA fragment from Bacillus subtilis 168 chromosomal DNA by PCR. The genes encoding endo-β-1,4-glucanase (eglS) and endo-β-1,3-1,4-glucanase (bglS) were isolated from a genomic library of B. subtilis 168. The sequences of xynA and eglS were identical to those of the xylanase and cellulase genes from B. subtilis PAP115. Integrative plasmids containing DNA fragments with deletions in the coding region of the genes were constructed and used to replace the chromosomal eglS, bglS and xynA genes of B. subtilis 168. Strains without any detectable activity against xylan (Xyn−), carboxymethylcellulose (Egl−) or mixed linked β-1,3-1,4-glucan (Egl− Bgl−) were obtained. The genes were mapped at 170° (eglS), 175° (xynA) and 340° (bglS) on theB. subtilischromosome.
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