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表达来自苏云金芽孢杆菌以色列亚种杀蚊毒素基因的鱼腥藻PCC7120在生物技术应用中的适用性。

Suitability of Anabaena PCC7120 expressing mosquitocidal toxin genes from Bacillus thuringiensis subsp. israelensis for biotechnological application.

作者信息

Lluisma A O, Karmacharya N, Zarka A, Ben-Dov E, Zaritsky A, Boussiba S

机构信息

Microalgal Biotechnology Laboratory, Blaustein Institute for Desert Research, Ben-Gurion University of the Negev, Israel.

出版信息

Appl Microbiol Biotechnol. 2001 Oct;57(1-2):161-6. doi: 10.1007/s002530100776.

Abstract

We present evidence that Anabaena PCC7120 (A.7120) strains expressing mosquitocidal toxin genes from Bacillus thuringiensis subsp. israelensis (Bti) have a strong potential for biotechnological application. Characterization of two 4-year-old recombinant A.7120 clones constructed previously in our laboratory [clone 7 and clone 11, each carrying three Bti genes (cry4Aa, cry11Aa, and p20)] revealed three facts. First, the Bti genes were stable in A.7120 even in the absence of antibiotic selection when the genes were integrated in the chromosome (in clone 11); and the genes were also stable as plasmid-borne constructs (in clone 7), provided the cultures were maintained under continued selection. Second, clone 7 (kept under selection) and clone 11 (either kept or not kept under selection) continued to be mosquitocidal through 4 years of culture. Third, growth of the recombinant clones was comparable to the wild type under optimal growth conditions, indicating that growth was not compromised by the expression of toxin genes. These results clear the way for the development of mass production techniques for A.7120 strains expressing Bti toxin genes.

摘要

我们提供的证据表明,表达来自苏云金芽孢杆菌以色列亚种(Bti)杀蚊毒素基因的鱼腥藻PCC7120(A.7120)菌株具有很强的生物技术应用潜力。对我们实验室之前构建的两个4岁重组A.7120克隆(克隆7和克隆11,每个携带三个Bti基因(cry4Aa、cry11Aa和p20))的表征揭示了三个事实。第一,当基因整合到染色体中时(在克隆11中),即使在没有抗生素选择的情况下,Bti基因在A.7120中也是稳定的;并且作为质粒携带构建体(在克隆7中),只要培养物在持续选择下维持,基因也是稳定的。第二,克隆7(保持在选择条件下)和克隆11(无论是否保持在选择条件下)经过4年培养仍具有杀蚊活性。第三,在最佳生长条件下,重组克隆的生长与野生型相当,这表明生长不受毒素基因表达的影响。这些结果为开发表达Bti毒素基因的A.7120菌株的大规模生产技术扫清了障碍。

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