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用于固氮蓝藻鱼腥藻PCC7120菌株改良及环境应用的整合表达载体。

An integrative expression vector for strain improvement and environmental applications of the nitrogen fixing cyanobacterium, Anabaena sp. strain PCC7120.

作者信息

Chaurasia Akhilesh Kumar, Parasnis Anjali, Apte Shree Kumar

机构信息

Molecular Biology Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400 085, India.

出版信息

J Microbiol Methods. 2008 May;73(2):133-41. doi: 10.1016/j.mimet.2008.01.013. Epub 2008 Feb 11.

Abstract

An integrative expression vector, incorporating a cassette for genomic integration and expression of gene of interest into Anabaena sp. strain PCC7120 was constructed. The cassette comprised of the following elements: (a) an intergenic non-coding region from Anabaena to facilitate its genomic integration (b) a strong functional PpsbA1 promoter from Anabaena for desired gene expression and (c) neomycin phosphotransferase gene with its own promoter for the selection of transformants. The cassette was cloned in the plasmid pBluescript II SK (+), which served as a suicide vector for Anabaena. The resultant plasmid designated as pFPN, when transferred into Anabaena by electrotransformation, integrated the cassette into Anabaena genome at the defined location. The vector was evaluated by cloning, transfer, integration and expression of the native hetR gene encoding a regulator of heterocyst differentiation. Formation of multiple heterocysts and enhanced nitrogenase activity of constitutively expressing hetR transformants of Anabaena established the utility of pFPN for basic molecular biology research and strain improvement. A transgene phoN encoding a non-specific acid phosphatase from Salmonella typhi was also transferred into Anabaena using pFPN. Strong constitutive expression of PhoN from PpsbA1 facilitated easier and sensitive visual screening of PhoN for tracking of transgenic Anabaena. The vector pFPN offers a stable integrative expression system for environmental application of genetically modified Anabaena strains.

摘要

构建了一种整合表达载体,该载体包含一个用于将感兴趣基因基因组整合并表达至鱼腥藻PCC7120菌株的盒式结构。该盒式结构由以下元件组成:(a) 来自鱼腥藻的基因间非编码区,以促进其基因组整合;(b) 来自鱼腥藻的强功能性PpsbA1启动子,用于所需基因的表达;(c) 带有自身启动子的新霉素磷酸转移酶基因,用于转化体的筛选。该盒式结构被克隆到质粒pBluescript II SK(+)中,该质粒用作鱼腥藻的自杀载体。所得质粒命名为pFPN,通过电转化转移到鱼腥藻中时,该盒式结构在特定位置整合到鱼腥藻基因组中。通过对编码异形胞分化调节因子的天然hetR基因进行克隆、转移、整合和表达来评估该载体。鱼腥藻组成型表达hetR的转化体中多个异形胞的形成和固氮酶活性的增强,证实了pFPN在基础分子生物学研究和菌株改良中的实用性。还使用pFPN将编码来自伤寒沙门氏菌的非特异性酸性磷酸酶的转基因phoN转移到鱼腥藻中。来自PpsbA1的PhoN的强组成型表达便于对PhoN进行更简便且灵敏的视觉筛选,以追踪转基因鱼腥藻。载体pFPN为转基因鱼腥藻菌株的环境应用提供了一个稳定的整合表达系统。

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