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根癌土壤杆菌Ti质粒中章鱼碱(occ)和胭脂碱(noc)分解代谢区域的冠瘿碱转运基因。

Opine transport genes in the octopine (occ) and nopaline (noc) catabolic regions in Ti plasmids of Agrobacterium tumefaciens.

作者信息

Zanker H, von Lintig J, Schröder J

机构信息

Institut für Biologie II, Universität Freiburg, Germany.

出版信息

J Bacteriol. 1992 Feb;174(3):841-9. doi: 10.1128/jb.174.3.841-849.1992.

Abstract

The occ and noc regions of octopine and nopaline Ti plasmids in Agrobacterium tumefaciens are responsible for the catabolic utilization of octopine and nopaline, respectively. Opine-inducible promoters, genes for regulatory proteins and for catabolic enzymes, had been identified in previous work. However, both regions contained additional DNA stretches which were under the control of opine-inducible promoters, but the functions were unknown. We investigated these stretches by DNA sequence and functional analyses. The sequences showed that both of the catabolic regions contain a set of four genes which are transcribed in the same direction. The occ and noc region genes are related, but the arrangement of the genes is different. The deduced polypeptides are related to those of binding protein-dependent transport systems of basic amino acids in other bacteria. The comparison suggested that three of the polypeptides are located in the membrane and that one is a periplasmic protein. We constructed cassettes which contained either the putative transport genes only or the complete occ or noc region; all constructs, however, included the elements necessary for opine-induced expression of the genes (the regulatory gene and the inducible promoters). Uptake studies with 3H-labelled octopine showed that the putative transport genes in the occ region code for octopine uptake proteins. The corresponding studies with 3H-labelled nopaline and the noc region cassettes indicated that the uptake of nopaline requires the putative transport genes and additional functions from the left part of the noc region.

摘要

根癌土壤杆菌中章鱼碱型和胭脂碱型Ti质粒的章鱼碱和胭脂碱区域分别负责章鱼碱和胭脂碱的分解代谢利用。在先前的研究中已经鉴定出了章鱼碱诱导型启动子、调节蛋白基因和分解代谢酶基因。然而,这两个区域都包含额外的DNA片段,这些片段受章鱼碱诱导型启动子的控制,但其功能尚不清楚。我们通过DNA序列和功能分析对这些片段进行了研究。序列分析表明,两个分解代谢区域都包含一组四个同向转录的基因。章鱼碱区域和胭脂碱区域的基因相关,但基因排列不同。推导的多肽与其他细菌中碱性氨基酸的依赖结合蛋白的转运系统的多肽相关。比较表明,其中三个多肽位于膜上,一个是周质蛋白。我们构建了仅包含推定转运基因或完整章鱼碱区域或胭脂碱区域的盒式结构;然而,所有构建体都包括基因的章鱼碱诱导表达所需的元件(调节基因和诱导型启动子)。用3H标记的章鱼碱进行的摄取研究表明,章鱼碱区域中的推定转运基因编码章鱼碱摄取蛋白。用3H标记的胭脂碱和胭脂碱区域盒式结构进行的相应研究表明,胭脂碱的摄取需要推定转运基因和来自胭脂碱区域左侧的其他功能。

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