Unité de Biochimie Microbienne, Institut Pasteur, 28, rue du Docteur Roux, 75724 Paris Cedex 15, and Station de Recherches de Lutte Biologique, Institut National de la Recherche Agronomique, La Minière, 78280 Guyancourt, France.
Appl Environ Microbiol. 1988 Nov;54(11):2689-98. doi: 10.1128/aem.54.11.2689-2698.1988.
At least three different insecticidal crystal protein genes were shown to be expressed in Bacillus thuringiensis subsp. aizawai 7.29, a strain that is potentially active against the cotton leafworm Spodoptera littoralis Bdv. Among crude K-60 fractions (60- to 70-kilodalton [kDa] molecules) that were products of proteolysed crystals containing the active domains of the protoxin molecules, we were able to distinguish several distinct components on the basis of their antigenic relationship and their larvicidal properties. A purified fraction designated SF2 was a 61-kDa component specifically active against Pieris brassicae L. and homologous to the B. thuringiensis subsp. berliner 1715 plasmid-encoded crystal protein. A second fraction designated SF1 was composed of 63- and 65-kDa polypeptides and was specifically active against S. littoralis. The SF1 fraction and particularly the 65-kDa component were not antigenically related to the 61-kDa component. The purified fractions were compared with the products of three different crystal protein genes we previously cloned from total DNA of B. thuringiensis subsp. aizawai, among them a new type of crystal protein gene encoding a protein that is specifically active against S. littoralis and other insects of the Noctuidae family. This approach led us to consider the 65-kDa component as a minimum active part of a delta-endotoxin that is encoded by this new gene. Products of the two other cloned genes can be correlated with the 61- and 63-kDa components, respectively. Thus, in B. thuringiensis subsp. aizawai 7.29, multiple delta-endotoxin genes of different structural types direct the synthesis of several delta-endotoxins with different host specificities which were identified as components of the insecticidal crystals.
苏云金芽孢杆菌亚种 aizawai 7.29 至少表达了三种不同的杀虫晶体蛋白基因,该菌株可能对棉铃虫 Spodoptera littoralis Bdv 有效。在含有原毒素分子活性结构域的晶体蛋白被蛋白水解后产生的粗 K-60 级分(60-70 千道尔顿 [kDa] 分子)中,我们能够根据其抗原关系和杀虫特性区分出几种不同的成分。一种纯化的 SF2 级分是一种 61-kDa 成分,对 Pieris brassicae L. 具有特异性活性,与 B. thuringiensis 亚种 berliner 1715 质粒编码的晶体蛋白同源。第二个级分 SF1 由 63-和 65-kDa 多肽组成,对 S. littoralis 具有特异性活性。SF1 级分,特别是 65-kDa 成分,与 61-kDa 成分没有抗原关系。纯化的级分与我们之前从苏云金芽孢杆菌亚种 aizawai 的总 DNA 中克隆的三个不同的晶体蛋白基因的产物进行了比较,其中包括一种新的晶体蛋白基因,该基因编码一种对 S. littoralis 和其他夜蛾科昆虫具有特异性活性的蛋白质。这种方法使我们认为 65-kDa 成分是由该新基因编码的 delta-内毒素的最小活性部分。两个其他克隆基因的产物可以分别与 61-和 63-kDa 成分相关联。因此,在苏云金芽孢杆菌亚种 aizawai 7.29 中,不同结构类型的多个 delta-内毒素基因指导合成了几种具有不同宿主特异性的 delta-内毒素,这些内毒素被鉴定为杀虫晶体的组成部分。