Identification and analysis of a static culture-specific cell wall protein, Tir1p/Srp1p in Saccharomyces cerevisiae

被引:40
作者
Kitagaki, H [1 ]
Shimoi, H [1 ]
Itoh, K [1 ]
机构
[1] NATL RES INST BREWING, HIGASHIHIROSHIMA 739, JAPAN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 249卷 / 01期
关键词
TIR1; SRP1; yeast cell wall protein; anaerobic conditions; Rarobacter faecitabidus protease I;
D O I
10.1111/j.1432-1033.1997.t01-1-00343.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A 100-kDa protein was found to be a major cell wall protein in Saccharomyces cerevisiae cells cultured without shaking, but was not present in cells cultured with shaking. The amino acid sequence of this protein was identical to the sequence of Tir1p/Srp1p. TIR1/SRP1 has previously been identified as a gene induced by glucose, cold shock or anaerobiosis and was believed to be a cell membrane protein but not a cell wall protein. However, we found that beta-1,3-glucanase solubilized Tir1p/Srp1p from the cell wall and the purified Tir1p/Srp1p reacted with antiserum to beta-1,6-glucan and contained glucose. These results suggest that Tir1p/Srp1p is a major structural cell wall protein in the static-cultured yeast cells and is bound to the cell wall through beta-1,6-glucan. TIR1/SRP1 mRNA was transcribed only in the static culture and its transcription was regulated by the ROX1 repressor.
引用
收藏
页码:343 / 349
页数:7
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