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嗜盐真养芽孢杆菌betH基因的克隆与特性分析,该基因编码相容性溶质甘氨酸甜菜碱的转运系统。

Cloning and characterization of the Halobacillus trueperi betH gene, encoding the transport system for the compatible solute glycine betaine.

作者信息

Lu Weidong, Zhao Baisuo, Feng Deqin, Yang Susheng

机构信息

Department of Microbiology, College of Biological Sciences, China Agricultural University and Key Laboratory of Agro-Microbial Resources and Application, Ministry of Agriculture, Beijing 100094, PR China.

出版信息

FEMS Microbiol Lett. 2004 Jun 15;235(2):393-9. doi: 10.1016/j.femsle.2004.05.015.

Abstract

Halobacillus trueperi accumulates glycine betaine under condition of high osmolarity. A fragment of the glycine betaine transporter betH gene was obtained from the genome of H. trueperi with degenerate primers. Through Southern blot hybridization and inverse PCR, a 5.1 kb EcoRI fragment containing the complete betH gene was identified and subsequently sequenced. The betH gene was predicted to encode a 55.2 kDa protein (504 amino acid residues) with 12 transmembrane regions. BetH showed 56% identity to the OpuD of Bacillus subtilis which belongs to the betaine/carnitine/choline transporter (BCCT) family. Its putative promoter region was highly homologous to sigmaB-dependent promoter of B. subtilis. A 2.6 kb fragment containing the betH gene was cloned into pUC18 and transformed into the Escherichia coli MKH13. The accumulation of glycine betaine in transformed E. coli MKH13 bacteria was confirmed using 13C nuclear magnetic resonance spectroscopy.

摘要

特鲁珀嗜盐芽孢杆菌在高渗透压条件下积累甘氨酸甜菜碱。利用简并引物从特鲁珀嗜盐芽孢杆菌基因组中获得了甘氨酸甜菜碱转运蛋白betH基因的一个片段。通过Southern杂交和反向PCR,鉴定出一个包含完整betH基因的5.1 kb EcoRI片段,并随后进行了测序。预测betH基因编码一个55.2 kDa的蛋白质(504个氨基酸残基),具有12个跨膜区域。BetH与枯草芽孢杆菌的OpuD具有56%的同一性,OpuD属于甜菜碱/肉碱/胆碱转运蛋白(BCCT)家族。其假定的启动子区域与枯草芽孢杆菌的σB依赖性启动子高度同源。将一个包含betH基因的2.6 kb片段克隆到pUC18中,并转化到大肠杆菌MKH13中。利用13C核磁共振波谱证实了转化后的大肠杆菌MKH13细菌中甘氨酸甜菜碱的积累。

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