Adams L F, Mathewes S, O'Hara P, Petersen A, Gürtler H
Novo Nordisk Biotech, Inc., Davis, California 95616.
Mol Microbiol. 1994 Oct;14(2):381-9. doi: 10.1111/j.1365-2958.1994.tb01298.x.
NB176 is a Bacillus thuringiensis mutant derived by gamma-irradiation of NB125 Bacillus thuringiensis var. tenebrionis (Krieg). It exhibits two interesting phenotypes: (i) oligosporogeny and (ii) twofold to threefold overproduction of the CryIIIA protein. Southern profiles of the NB176 strain showed an additional copy(s) of the cryIIIA gene located on a 4 kb HindIII fragment, in addition to the expected cryIIIA gene on a 3 kb HindIII fragment. Each cryIIIA gene-bearing HindIII fragment was cloned from NB176. The restriction map of the 3 kb HindIII fragment was identical to that published by Donovan and coworkers. Sequencing of the 4 kb HindIII fragment showed no alterations in the promoter region of the cryIIIA gene but did show replacement of the region immediately following the cryIIIA open reading frame with a sequence encoding a transposase with 50% amino acid homology to that of Tn1000. These findings suggest that the overproduction phenotype of NB176 results from extra copies of the cryIIIA gene produced from a transposition event(s) induced or stabilized by gamma-irradiation. Integration of additional copies of the cryIIIA gene into the native 90 MDa plasmid of the wild-type B. thuringiensis var. tenebrionis strain resulted in strains that made enormous crystals, many possessing greatly enhanced insecticidal activity.
NB176是通过对苏云金芽孢杆菌变种暗黑变种(Krieg)的NB125进行γ射线辐照而获得的苏云金芽孢杆菌突变体。它表现出两种有趣的表型:(i)少孢形成,以及(ii)CryIIIA蛋白产量增加两到三倍。NB176菌株的Southern杂交图谱显示,除了位于3 kb HindIII片段上预期的cryIIIA基因外,在4 kb HindIII片段上还存在cryIIIA基因的额外拷贝。从NB176中克隆了每个携带cryIIIA基因的HindIII片段。3 kb HindIII片段的限制性图谱与Donovan及其同事发表的图谱相同。对4 kb HindIII片段的测序表明,cryIIIA基因的启动子区域没有改变,但确实显示cryIIIA开放阅读框之后的区域被一个编码转座酶的序列所取代,该转座酶与Tn1000的氨基酸同源性为50%。这些发现表明,NB176的过量生产表型是由γ射线辐照诱导或稳定的转座事件产生的cryIIIA基因额外拷贝所致。将cryIIIA基因的额外拷贝整合到野生型苏云金芽孢杆菌变种暗黑变种菌株的天然90 MDa质粒中,产生了形成巨大晶体的菌株,其中许多菌株具有大大增强的杀虫活性。