Takagi H, Shichiri M, Takemura M, Mohri M, Nakamori S
Department of Bioscience, Fukui Prefectural University, Matsuoka-cho, Fukui 910-1195, Japan.
J Bacteriol. 2000 Aug;182(15):4249-56. doi: 10.1128/JB.182.15.4249-4256.2000.
We discovered on the chromosome of Saccharomyces cerevisiae Sigma 1278b novel genes involved in L-proline analogue L-azetidine-2-carboxylic acid resistance which are not present in the standard laboratory strains. The 5.4 kb-DNA fragment was cloned from the genomic library of the L-azetidine-2-carboxylic acid-resistant mutant derived from a cross between S. cerevisiae strains S288C and Sigma 1278b. The nucleotide sequence of a 4.5-kb segment exhibited no identity with the sequence in the genome project involving strain S288C. Deletion analysis indicated that one open reading frame encoding a predicted protein of 229 amino acids is indispensable for L-azetidine-2-carboxylic acid resistance. The protein sequence was found to be a member of the N-acetyltransferase superfamily. Genomic Southern analysis and gene disruption showed that two copies of the novel gene with one amino acid change at position 85 required for L-azetidine-2-carboxylic acid resistance were present on chromosomes X and XIV of Sigma 1278b background strains. When this novel MPR1 or MPR2 gene (sigma 1278b gene for L-proline analogue resistance) was introduced into the other S. cerevisiae strains, all of the recombinants were resistant to L-azetidine-2-carboxylic acid, indicating that both MPR1 and MPR2 are expressed and have a global function in S. cerevisiae.
我们在酿酒酵母Sigma 1278b的染色体上发现了与L-脯氨酸类似物L-氮杂环丁烷-2-羧酸抗性相关的新基因,这些基因在标准实验室菌株中不存在。从酿酒酵母菌株S288C和Sigma 1278b杂交产生的L-氮杂环丁烷-2-羧酸抗性突变体的基因组文库中克隆出5.4 kb的DNA片段。一个4.5 kb片段的核苷酸序列与涉及菌株S288C的基因组计划中的序列没有同源性。缺失分析表明,一个编码预测的229个氨基酸的蛋白质的开放阅读框对于L-氮杂环丁烷-2-羧酸抗性是必不可少的。该蛋白质序列被发现是N-乙酰转移酶超家族的成员。基因组Southern分析和基因破坏表明,在Sigma 1278b背景菌株的X和XIV染色体上存在两个L-氮杂环丁烷-2-羧酸抗性所需的在第85位有一个氨基酸变化的新基因拷贝。当这个新的MPR1或MPR2基因(用于L-脯氨酸类似物抗性的sigma 1278b基因)被导入其他酿酒酵母菌株时,所有重组体都对L-氮杂环丁烷-2-羧酸有抗性,这表明MPR1和MPR2在酿酒酵母中都有表达并具有全局功能。