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首页> 外文期刊>Applied and Environmental Microbiology >Molecular cloning, sequence analysis, and expression of the yeast alcohol acetyltransferase gene.
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Molecular cloning, sequence analysis, and expression of the yeast alcohol acetyltransferase gene.

机译:酵母醇乙酰基转移酶基因的分子克隆,序列分析和表达。

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摘要

The ATF1 gene, which encodes alcohol acetyltransferase (AATase), was cloned from Saccharomyces cerevisiae and brewery lager yeast (Saccharomyces uvarum). The nucleotide sequence of the ATF1 gene isolated from S. cerevisiae was determined. The structural gene consists of a 1,575-bp open reading frame that encodes 525 amino acids with a calculated molecular weight of 61,059. Although the yeast AATase is considered a membrane-bound enzyme, the results of a hydrophobicity analysis suggested that this gene product does not have a membrane-spanning region that is significantly hydrophobic. A Southern analysis of the yeast genomes in which the ATF1 gene was used as a probe revealed that S. cerevisiae has one ATF1 gene, while brewery lager yeast has one ATF1 gene and another, homologous gene (Lg-ATF1). Transformants carrying multiple copies of the ATF1 gene or the Lg-ATF1 gene exhibited high AATase activity in static cultures and produced greater concentrations of acetate esters than the control.
机译:从啤酒酵母和啤酒酵母(Saccharomyces uvarum)克隆了编码乙醇乙酰基转移酶(AATase)的ATF1基因。确定了从酿酒酵母分离的ATF1基因的核苷酸序列。结构基因由一个1,575 bp的开放阅读框组成,该阅读框编码525个氨基酸,计算的分子量为61,059。尽管酵母AATase被认为是膜结合酶,但是疏水性分析的结果表明该基因产物没有明显疏水的跨膜区域。对使用ATF1基因作为探针的酵母基因组的Southern分析显示,酿酒酵母具有一个ATF1基因,而啤酒啤酒则具有一个ATF1基因和另一个同源基因(Lg-ATF1)。携带多个ATF1基因或Lg-ATF1基因拷贝的转化子在静态培养物中显示出高的AATase活性,并且比对照产生更高浓度的乙酸酯。

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