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丁香假单胞菌毒素生物合成所需tblA基因的DNA序列及转录分析

DNA sequence and transcriptional analysis of the tblA gene required for tabtoxin biosynthesis by Pseudomonas syringae.

作者信息

Barta T M, Kinscherf T G, Uchytil T F, Willis D K

机构信息

Department of Plant Pathology, University of Wisconsin, Madison 53706.

出版信息

Appl Environ Microbiol. 1993 Feb;59(2):458-66. doi: 10.1128/aem.59.2.458-466.1993.

Abstract

The tblA gene of Pseudomonas syringae is required for tabtoxin biosynthesis and is under the control of a regulatory gene, lemA. We have determined the nucleotide sequence of the tblA gene and identified the 5' end of the tblA gene transcript. The sequence of the tblA gene was identified to that of the recently reported open reading frame 1 gene of the tabA region of the BR2 chromosome. The open reading frame of the tblA gene potentially encodes a protein of 231 amino acids. mRNA from the tblA gene was detected at all phases of cells grown in minimal medium. This result is correlated with the constitutive production of tabtoxinine-beta-lactam (the biologically active part of the toxin) by P. syringae BR2R in minimal medium, as quantitated by a phenylisothiocyanate derivatization method.

摘要

丁香假单胞菌的tblA基因是烟草毒素生物合成所必需的,并且受调控基因lemA的控制。我们已经确定了tblA基因的核苷酸序列,并鉴定出tblA基因转录本的5'端。tblA基因的序列与最近报道的BR2染色体tabA区域的开放阅读框1基因的序列一致。tblA基因的开放阅读框可能编码一个由231个氨基酸组成的蛋白质。在基本培养基中生长的细胞的所有阶段都检测到了来自tblA基因的mRNA。这一结果与通过异硫氰酸苯酯衍生化法测定的丁香假单胞菌BR2R在基本培养基中组成型产生烟草毒素-β-内酰胺(毒素的生物活性部分)相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb3/202127/3d439b1fb0d6/aem00031-0119-a.jpg

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