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Polycistronic strategy for cyanobacterial expression vector construction: Co-transcription of a human gene and a selective marker gene

机译:蓝细菌表达载体构建的多顺反子策略:人类基因和选择标记基因的共转录

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A polycistronic expression vector, pKGA-NTFl, was constructed for the cyanobacterium. Within this vector, the spectinomycin/streptomycin resistance gene (aadA) facilitated the selection of transformants when co-transcribed with favorite genes. A natural glnA gene was selected as the platform to introduce the plasmid into a neutral site of the Synechncoccus sp. PCC 7002 chromosome. Function of the vector was demonstrated by the insertion of a modified human Trefoil factor 3 gene (NTF1) to upstream ofthe aadA gene and by the analyses of the transformed strains. Antibiotics resistance assays showed that the dicistronic expression cassette conferred high spectinomycin resistance to both the E. coli cells and the Synechococcus cells. PCR analysis and Western-blot analysis were carried out to confirm the integration and expression of the NTF1 gene, respectively. Through simple molecular manipulations, the artificial polycistronic structure described here can be conveniently used to express other favorable genes or operons in cyanobacteria, and to study the cyanobacterial gene expression as well.
机译:为蓝细菌构建了多顺反子表达载体pKGA-NTF1。在该载体内,大观霉素/链霉素抗性基因(aadA)与喜好的基因共转录时有助于转化子的选择。选择天然的glnA基因作为平台,以将质粒引入到Syneechncoccus sp的中性位点。 PCC 7002染色体。通过将修饰的人三叶因子3基因(NTF1)插入aadA基因上游并通过分析转化菌株来证明载体的功能。抗生素抗药性分析表明,双顺反子表达盒对大肠杆菌细胞和Synocococcus细胞均具有高壮观霉素抗性。进行PCR分析和蛋白质印迹分析以分别确认NTF1基因的整合和表达。通过简单的分子操作,此处描述的人工多顺反子结构可方便地用于在蓝细菌中表达其他有利的基因或操纵子,以及研究蓝细菌基因的表达。

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