Wolf M, Geczi A, Simon O, Borriss R
Institut für Biologie, Humboldt Universität, Berlin, Germany.
Microbiology (Reading). 1995 Feb;141 ( Pt 2):281-90. doi: 10.1099/13500872-141-2-281.
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-beta-1,4-glucanase (eglS) and endo-beta-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 beta-1,3-1,4-glucan (Egl- Bgl-) were obtained. The genes were mapped at 170 degrees (eglS), 175 degrees (xynA) and 340 degrees (bglS) on the B. subtilis chromosome.
通过PCR从枯草芽孢杆菌168染色体DNA中扩增出编码胞外木聚糖酶(xynA)的基因,其为一个770 bp的DNA片段。从枯草芽孢杆菌168的基因组文库中分离出编码内切β-1,4-葡聚糖酶(eglS)和内切β-1,3-1,4-葡聚糖酶(bglS)的基因。xynA和eglS的序列与枯草芽孢杆菌PAP115的木聚糖酶和纤维素酶基因的序列相同。构建了在基因编码区带有缺失的DNA片段的整合质粒,并用于替换枯草芽孢杆菌168的染色体eglS、bglS和xynA基因。获得了对木聚糖(Xyn-)、羧甲基纤维素(Egl-)或混合连接的β-1,3-1,4-葡聚糖(Egl- Bgl-)没有任何可检测活性的菌株。这些基因在枯草芽孢杆菌染色体上分别定位在170度(eglS)、175度(xynA)和340度(bglS)处。