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来自台湾粮仓的苏云金芽孢杆菌G10-01A杀虫晶体蛋白基因Cry1Ca9的克隆与表达

Cloning and expression of the insecticidal crystal protein gene Cry1Ca9 of Bacillus thuringiensis G10-01A from Taiwan granaries.

作者信息

Kao Suey-Sheng, Hsieh Feng-Chia, Tzeng Ching-Chou, Tsai Yeong-Sheng

机构信息

Biopesticide Department, Taiwan Agricultural Chemicals and Toxic Substances Research Institute, Council of Agriculture, Wufeng, Taichung Hsien 41301, Taiwan.

出版信息

Curr Microbiol. 2003 Oct;47(4):295-9. doi: 10.1007/s00284-002-3982-4.

Abstract

A new cry gene (cry1Ca9) was cloned and sequenced from a Bacillus thuringiensis isolate native to Taiwan (G10-01A). The cry1C-type gene, designated cry1Ca9, consisted of an open reading frame of 3,567 bp, encoding a protein of 1,189 amino acid residues. The polypeptide has the deduced amino acid sequences predicting molecular masses of 134.7 kDa. The gene sequence was compared against the GenBank nucleotide sequence data base. It was found that the cry1Ca9 gene coded for a 134.7-kDa protoxin which had greater than 99.8% homology with the previously reported cry1Ca1 gene, as only three mismatches were found between the two amino acid sequences. When the Cry1Ca9 toxin was expressed in a crystal-negative strain of B. thuringiensis (cryB-), elliptical crystals were produced. Cell extracts from this recombinant strain appear to have high insecticidal activity against lepidopteran larvae (Plutella xylostella).

摘要

从台湾本地的苏云金芽孢杆菌分离株(G10 - 01A)中克隆并测序了一个新的cry基因(cry1Ca9)。这个cry1C型基因,命名为cry1Ca9,由一个3567 bp的开放阅读框组成,编码一个含有1189个氨基酸残基的蛋白质。该多肽推导的氨基酸序列预测分子量为134.7 kDa。将该基因序列与GenBank核苷酸序列数据库进行比较。发现cry1Ca9基因编码一种134.7 kDa的原毒素,与先前报道的cry1Ca1基因具有大于99.8%的同源性,因为在两个氨基酸序列之间仅发现三个错配。当Cry1Ca9毒素在苏云金芽孢杆菌的一个晶体阴性菌株(cryB -)中表达时,产生了椭圆形晶体。该重组菌株的细胞提取物似乎对鳞翅目幼虫(小菜蛾)具有高杀虫活性。

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