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决定质粒介导的柠檬酸盐利用的基因的核苷酸序列。

Nucleotide sequence of the gene determining plasmid-mediated citrate utilization.

作者信息

Ishiguro N, Sato G

出版信息

J Bacteriol. 1985 Dec;164(3):977-82. doi: 10.1128/jb.164.3.977-982.1985.

Abstract

The citrate utilization determinant from transposon Tn3411 has been cloned and sequenced, and its polypeptide products have been characterized in minicell experiments. The nucleotide sequence was determined for a 2,047-base-pair BglII restriction endonuclease fragment that includes the citrate determinant. This region contains an open reading frame that would encode a 431-amino-acid very hydrophobic polypeptide and which is preceded by a reasonable ribosomal binding site. However, the single polypeptide found in minicell experiments had an apparent molecular weight of 35,000 on sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

摘要

来自转座子Tn3411的柠檬酸盐利用决定簇已被克隆和测序,其多肽产物已在小细胞实验中得到表征。测定了一个包含柠檬酸盐决定簇的2047个碱基对的BglII限制性内切酶片段的核苷酸序列。该区域包含一个开放阅读框,它将编码一个431个氨基酸的非常疏水的多肽,并且在其前面有一个合理的核糖体结合位点。然而,在小细胞实验中发现的单一多肽在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上的表观分子量为35000。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cb9/219287/184bae453c50/jbacter00217-0013-a.jpg

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