将曲霉霉根特异性Asy启动子及编码几丁质酶42 kDa的基因克隆到植物表达载体上

Nguyen Hoang Tue, Tran Gia Cat Tuong, P. Trang, Nguyen-Duc Chung, hung Thi Bich Hoa, Nguyen Quang Duc Tien, N. Loc
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引用次数: 4

摘要

本研究的目的是构建含有几丁质酶基因和根特异性启动子的植物抗植物病原真菌表达载体。几丁质酶的信号肽基因Chi42、syncodChi42-1和syncodChi42-2被用于本研究。Chi42是曲霉木霉(Trichoderma asperellum) SH16的一个野生型基因,syncodChi42-1和syncodChi42-2基因均来源于Chi42,并经过优化,可以使用密码子进行植物表达。本研究采用分子克隆的方法。成功构建了几丁质酶基因表达载体pNHL20、Chi42基因表达载体pNHL20.1、syncodChi42-1基因表达载体pNHL20.2、syncodChi42-2基因表达载体pNHL20.3,并将其转入农杆菌LBA 4404中。携带几丁质酶基因的瘤胃杆菌已准备好进行花生(arachhis hypogaea L.)的遗传转化,以供后续应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning the root-specific Asy promoter and genes encoding chitinase 42 kDa of Trichoderma asperellum into the plant expression vector
The objective of the present study was to construct plant expression vectors containing chitinase genes and root-specific promoters for resistance to phytopathogenic fungi. Chitinase genes with a signal peptide sequence, such as Chi42 , syncodChi42-1 , and syncodChi42-2 , were used in this work. Chi42 is a wild-type gene of Trichoderma asperellum SH16, and both syncodChi42-1 and syncodChi42-2 genes are derived from Chi42, which have been optimized for the use of codon for plant expression. Methods of molecular cloning were applied in this study. The plant expression vectors pNHL20 containing chitinase genes, pNHL20.1 for Chi42 , pNHL20.2 for syncodChi42-1 , and pNHL20.3 for syncodChi42-2 , were successfully constructed and transferred into Agrobacterium tumefaciens LBA 4404. Bacteria A. tumefaciens harboring the chitinase genes are ready for genetic transformation to peanuts ( Arachis hypogaea L.) for subsequent applications.
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