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酿酒酵母显性絮凝基因FLO8的分子克隆与分析

Molecular cloning and analysis of the dominant flocculation gene FLO8 from Saccharomyces cerevisiae.

作者信息

Kobayashi O, Suda H, Ohtani T, Sone H

机构信息

Central Laboratories for Key Technology, Kirin Brewery Co. Ltd., Kanagawa, Japan.

出版信息

Mol Gen Genet. 1996 Jul 26;251(6):707-15. doi: 10.1007/BF02174120.

Abstract

A flocculation gene was cloned from a Saccharomyces cerevisiae ATCC60715 genomic library, known to contain the FLO8 gene, on the basis of its ability to confer a flocculation phenotype on a nonflocculent strain. From a total of 11 130 clones, four clones sharing the several restriction fragments were isolated, suggesting that these were derived from the same locus. The results of integration mapping and disruption of the cloned gene indicated that this gene was the FLO8 gene. After disruption of the FLO8 gene, the strain lost its ability to flocculate. The DNA sequence of the FLO8 gene was determined. This gene includes a 2187-bp open reading frame that encodes a 729-amino acid protein. Computer analysis indicated that the FLO8 gene has a significant degree of homology with a S. cerevisiae chromosome V DNA sequence, but no homology with the FLO1 gene. The hydrophobicity profile of the putative FLO8 gene product did not indicate the presence of any significantly hydrophobic regions. Southern analysis of the FLO8 gene present in various yeast strains indicated that the FLO8 gene is highly conserved in yeast strains having a variety of flocculation phenotypes and genotypes. Northern analysis revealed that the level of FLO1 gene transcription is dependent on the rate of transcription of the FLO8 gene. These results suggest that the FLO8 gene mediates flocculation via transcriptional activation of the FLO1 gene.

摘要

基于其能赋予非絮凝菌株絮凝表型的能力,从已知含有FLO8基因的酿酒酵母ATCC60715基因组文库中克隆出一个絮凝基因。从总共11130个克隆中,分离出四个共享几个限制性片段的克隆,这表明它们来自同一基因座。克隆基因的整合图谱绘制和破坏结果表明该基因就是FLO8基因。破坏FLO8基因后,该菌株失去了絮凝能力。测定了FLO8基因的DNA序列。该基因包含一个2187bp的开放阅读框,编码一个729个氨基酸的蛋白质。计算机分析表明,FLO8基因与酿酒酵母第五条染色体的DNA序列有显著的同源性,但与FLO1基因没有同源性。推测的FLO8基因产物的疏水性图谱未显示存在任何明显的疏水区域。对各种酵母菌株中存在的FLO8基因进行的Southern分析表明,FLO8基因在具有各种絮凝表型和基因型的酵母菌株中高度保守。Northern分析显示,FLO1基因的转录水平取决于FLO8基因的转录速率。这些结果表明,FLO8基因通过对FLO1基因的转录激活来介导絮凝。

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