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乳酸克鲁维酵母老黄色酶编码基因的核苷酸序列及染色体定位

Nucleotide sequence and chromosomal localization of the gene encoding the Old Yellow Enzyme from Kluyveromyces lactis.

作者信息

Miranda M, Ramírez J, Guevara S, Ongay-Larios L, Peña A, Coria R

机构信息

Departamento de Microbiología, Universidad Nacional Autónoma de México, México, DF.

出版信息

Yeast. 1995 Apr 30;11(5):459-65. doi: 10.1002/yea.320110509.

Abstract

A 6.6 kb genomic DNA fragment from the yeast Kluyveromyces lactis was isolated. Sequence analysis of this fragment revealed the presence of two incomplete open reading frames (ORFs) in one strand, one coding for the carboxyl terminus of the plasma membrane H(+)-ATPase and the other for the amino terminus of an unidentified product. In the complementary strand, a full-length ORF which encodes for a protein homologous to the yeast NADPH-dependent Old Yellow Enzyme was found. The deduced amino acid sequence of this ORF predicts a protein of 398 residues with 84% similarity in its full length to OYE1 from Saccharomyces carlsbergensis and OYE2 from Saccharomyces cerevisiae. In addition, an internal region showed considerable similarity to the bile acid-inducible polypeptide from Eubacterium sp., to the NADH oxidase from Thermoanaerobium brockii, to the trimethylamino dehydrogenase from bacterium W3A1 and to the estrogen-binding protein from Candida albicans, suggesting a functional or structural relationship between them. Inactivation of the KYE1 (Kluyveromyces Yellow Enzyme) gene by deletion of 0.6 kb fragment between positions +358 and +936 produced viable cells with a slight increase in their generation time. Haploid cells carrying the disrupted allele showed one-third of the NADPH oxidase activity, compared to wild-type cells. Southern blotting analysis of digested DNA and chromosomes separated by contour-clamped homogeneous electric field electrophoresis from K. lactis indicated that this is a single-copy gene and it is localized on chromosome II, whose molecular size has been estimated to be approximately 1.3 Mb.

摘要

从乳酸克鲁维酵母中分离出一段6.6 kb的基因组DNA片段。对该片段的序列分析显示,一条链上存在两个不完整的开放阅读框(ORF),一个编码质膜H(+)-ATPase的羧基末端,另一个编码一种未鉴定产物的氨基末端。在互补链中,发现了一个全长ORF,它编码一种与酵母NADPH依赖性老黄酶同源的蛋白质。该ORF推导的氨基酸序列预测其为一个含有398个残基的蛋白质,其全长与卡尔斯伯酵母中的OYE1和酿酒酵母中的OYE2有84%的相似性。此外,一个内部区域与真细菌属的胆汁酸诱导多肽、布氏嗜热厌氧菌的NADH氧化酶、细菌W3A1的三甲胺脱氢酶以及白色念珠菌的雌激素结合蛋白有相当的相似性,表明它们之间存在功能或结构关系。通过缺失+358和+936位之间的0.6 kb片段使KYE1(克鲁维酵母黄酶)基因失活,产生了生长时间略有增加的活细胞。与野生型细胞相比,携带破坏等位基因的单倍体细胞显示出三分之一的NADPH氧化酶活性。对乳酸克鲁维酵母经轮廓夹钳均匀电场电泳分离的消化DNA和染色体进行Southern印迹分析表明,这是一个单拷贝基因,它位于II号染色体上,其分子大小估计约为1.3 Mb。

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