Donovan W P, Rupar M J, Slaney A C, Malvar T, Gawron-Burke M C, Johnson T B
Ecogen Inc., Langhorne, Pennsylvania 19047.
Appl Environ Microbiol. 1992 Dec;58(12):3921-7. doi: 10.1128/aem.58.12.3921-3927.1992.
Bacillus thuringiensis EG2838 and EG4961 are highly toxic to Colorado potato beetle larvae, and only strain EG4961 is toxic to southern corn rootworm larvae. To investigate the cause of the different insecticidal activities of EG2838 and EG4961, cryIII-type genes toxic to coleopterans were cloned from each strain. The cryIIIB gene, cloned as part of an 8.0-kb EcoRI fragment of EG2838 DNA, encoded a crystal protein (CryIIIB) of 74,237 Da. The cryIIIB2 gene, cloned as part of an 8.3-kb PstI-Asp718 fragment of EG4961 DNA, encoded a crystal protein (CryIIIB2) of 74,393 Da that was 94% identical to CryIIIB. Analysis of the transcriptional start sites showed that cryIIIB and cryIIIB2 were initiated from a conserved region located within 130 nucleotides upstream from the translation start sites of both genes. Although the CryIIIB and CryIIIB2 proteins were similar in sequence, they displayed distinct insecticidal activities: CryIIIB was one-third as toxic as CryIIIB2 to Colorado potato beetle larvae, and CryIIIB2, but not CryIIIB, was toxic to southern corn rootworm larvae. Genes encoding crystal proteins of approximately 32 and 31 kDa were located adjacent to the cryIIIB and cryIIIB2 genes, respectively. The 32- and 31-kDa crystal proteins failed to enhance the insecticidal activities of CryIIIB and CryIIIB2.
苏云金芽孢杆菌EG2838和EG4961对科罗拉多马铃薯甲虫幼虫具有高毒性,并且只有菌株EG4961对南部玉米根虫幼虫有毒性。为了研究EG2838和EG4961杀虫活性不同的原因,从每个菌株中克隆了对鞘翅目昆虫有毒的cryIII型基因。作为EG2838 DNA的一个8.0 kb EcoRI片段的一部分克隆的cryIIIB基因,编码一种74,237 Da的晶体蛋白(CryIIIB)。作为EG4961 DNA的一个8.3 kb PstI-Asp718片段的一部分克隆的cryIIIB2基因,编码一种74,393 Da的晶体蛋白(CryIIIB2),它与CryIIIB有94%的同一性。转录起始位点分析表明,cryIIIB和cryIIIB2从位于两个基因翻译起始位点上游130个核苷酸内的一个保守区域起始。尽管CryIIIB和CryIIIB2蛋白在序列上相似,但它们表现出不同的杀虫活性:CryIIIB对科罗拉多马铃薯甲虫幼虫的毒性是CryIIIB2的三分之一,并且CryIIIB2对南部玉米根虫幼虫有毒性,而CryIIIB则没有。分别与cryIIIB和cryIIIB2基因相邻定位了编码约32 kDa和31 kDa晶体蛋白的基因。32 kDa和31 kDa的晶体蛋白未能增强CryIIIB和CryIIIB2的杀虫活性。