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来自耐盐酵母汉逊德巴利酵母的多个p450alk(细胞色素P450烷烃羟化酶)基因。

Multiple p450alk (cytochrome P450 alkane hydroxylase) genes from the halotolerant yeast Debaryomyces hansenii.

作者信息

Yadav J S, Loper J C

机构信息

Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati Medical Center, Cincinnati, OH 45267-0524,

出版信息

Gene. 1999 Jan 21;226(2):139-46. doi: 10.1016/s0378-1119(98)00579-4.

DOI:10.1016/s0378-1119(98)00579-4
PMID:9931473
Abstract

The halotolerant alkane-assimilating yeast Debaryomyces hansenii was examined for P450 alkane hydroxylase genes known to be required for alkane assimilation in Candida. Four distinct P450alk gene segments and an allelic segment were isolated using PCR based on degenerate primers derived from the CYP52 family of alkane-inducible P450 genes. A screen of a genomic library (15-20kb inserts) constructed for this study, using a probe based on the PCR-isolated segments, yielded seven clones. This has led to the isolation and sequence of two full-length genes DH-ALK1 and DH-ALK2. These genes, each with an ORF of 1557 bp (519 aa), contained no apparent introns and showed 64% nucleotide sequence homology (61% based on the deduced amino acid sequences). The deduced proteins had predicted molecular weights of 59,254Da (DH-ALK1) and 59,614Da (DH-ALK2) and have been designated CYP52A12 and CYP52A13 by the P450 Nomenclature Committee. Phylogenetic analysis based on Neighbor Joining Tree showed that DH-ALK1 and DH-ALK2 constitute new genes located on two distinct branches and are most related to the gene CYP52A3 (60% deduced aa homology) and are least related to the gene CYP52C2 (41% deduced aa homology), both of C. maltosa. The isolated genes will provide tools to better understand the diversity of the P450alk family in eukaryotic microorganisms adapted to varied environmental conditions.

摘要

对耐盐烷烃同化酵母汉逊德巴利酵母进行了检测,以寻找已知在假丝酵母中烷烃同化所需的P450烷烃羟化酶基因。基于来自烷烃诱导型P450基因的CYP52家族的简并引物,利用PCR分离出四个不同的P450alk基因片段和一个等位基因片段。使用基于PCR分离片段的探针,对本研究构建的基因组文库(15 - 20kb插入片段)进行筛选,得到了七个克隆。这导致了两个全长基因DH - ALK1和DH - ALK2的分离和测序。这些基因,每个都有一个1557 bp(519个氨基酸)的开放阅读框,没有明显的内含子,核苷酸序列同源性为64%(基于推导的氨基酸序列为61%)。推导的蛋白质预测分子量分别为59,254Da(DH - ALK1)和59,614Da(DH - ALK2),并被P450命名委员会指定为CYP52A12和CYP52A13。基于邻接树的系统发育分析表明,DH - ALK1和DH - ALK2构成了位于两个不同分支上的新基因,与麦芽假丝酵母的基因CYP52A3关系最为密切(推导的氨基酸同源性为60%),与基因CYP52C2关系最不密切(推导的氨基酸同源性为41%)。分离出的基因将为更好地理解适应不同环境条件的真核微生物中P450alk家族的多样性提供工具。

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