Ben-Dov E, Einav M, Peleg N, Boussiba S, Zaritsky A
Department of Life Sciences, Ben-Gurion University of the Negev, Be'er-Sheva, Israel.
Appl Environ Microbiol. 1996 Sep;62(9):3140-5. doi: 10.1128/aem.62.9.3140-3145.1996.
A large plasmid containing all delta-endotoxin genes was isolated from Bacillus thuringiensis subsp. israelensis; restricted by BamHI, EcoRI, HindIII, KpnI, PstI, SacI, and SalI; and cloned as appropriate libraries in Escherichia coli. The libraries were screened for inserts containing recognition sites for BamHI, SacI, and SalI. Each was labeled with 32P and hybridized to Southern blots of gels with fragments generated by cleaving the plasmid with several restriction endonucleases, to align at least two fragments of the relevant enzymes. All nine BamHI fragments and all eight SacI fragments were mapped in two overlapping linkage groups (with total sizes of about 76 and 56 kb, respectively). The homology observed between some fragments is apparently a consequence of the presence of transposons and repeated insertion sequences. Four delta-endotoxin genes (cryIVB-D and cytA) and two genes for regulatory polypeptides (of 19 and 20 kDa) were localized on a 21-kb stretch of the plasmid; without cytA, they are placed on a single BamHI fragment. This convergence enables subcloning of delta-endotoxin genes (excluding cryIVA, localized on the other linkage group) as an intact natural fragment.
从苏云金芽孢杆菌以色列亚种中分离出一个包含所有δ-内毒素基因的大质粒;用BamHI、EcoRI、HindIII、KpnI、PstI、SacI和SalI进行酶切;并在大肠杆菌中构建了合适的文库。筛选文库中含有BamHI、SacI和SalI识别位点的插入片段。每个片段都用32P标记,并与用几种限制性内切酶切割质粒产生的凝胶Southern印迹杂交,以使至少两个相关酶的片段对齐。所有九个BamHI片段和所有八个SacI片段被定位在两个重叠的连锁群中(总大小分别约为76 kb和56 kb)。一些片段之间观察到的同源性显然是转座子和重复插入序列存在的结果。四个δ-内毒素基因(cryIVB - D和cytA)和两个调节多肽基因(分别为19 kDa和20 kDa)定位在质粒的一段21 kb区域;如果没有cytA,它们位于单个BamHI片段上。这种聚集使得δ-内毒素基因(不包括位于另一个连锁群上的cryIVA)能够作为一个完整的天然片段进行亚克隆。