Heterologous expression of a plant ReIA-SpoT homologue results in increased stress tolerance in Saccharomyces cerevisiae by accumulation of the bacterial alarmone ppGpp

被引:9
作者
Ochi, Kozo [1 ,2 ]
Nishizawa, Tomoyasu [2 ]
Inaoka, Takashi [2 ]
Yamada, Akiyo [3 ]
Hashimoto, Kohsuke [1 ]
Hosaka, Takeshi [4 ]
Okamoto, Susumu [2 ]
Ozeki, Yoshihiro [3 ]
机构
[1] Hiroshima Inst Technol, Dept Life Sci, Saeki Ku, Hiroshima 7315193, Japan
[2] Natl Food Res Inst, Tsukuba, Ibaraki 3058642, Japan
[3] Tokyo Univ Agr & Technol, Fac Technol, Dept Biotechnol, Koganei, Tokyo 1848588, Japan
[4] Shinshu Univ, Int Young Researchers Empowerment Ctr, Nagano 3994598, Japan
来源
MICROBIOLOGY-SGM | 2012年 / 158卷
关键词
STREPTOMYCES-COELICOLOR A3(2); GUANOSINE 5'-DIPHOSPHATE 3'-DIPHOSPHATE; STRINGENT RESPONSE; ESCHERICHIA-COLI; BACILLUS-SUBTILIS; PSEUDOMONAS-AERUGINOSA; ANTIBIOTIC PRODUCTION; STATIONARY-PHASE; TRANSCRIPTION REGULATION; SECONDARY METABOLISM;
D O I
10.1099/mic.0.057638-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The bacterial alarmone ppGpp is present only in bacteria and the chloroplasts of plants, but not in mammalian cells or eukaryotic micro-organisms such as yeasts and fungi. The importance of the ppGpp signalling system in eukaryotes has therefore been largely overlooked. Here, we demonstrated that heterologous expression of a reIA-spoT homologue (Sj-RSH) isolated from the halophilic plant Suaeda japonica in the yeast Saccharomyces cerevisiae results in accumulation of ppGpp, accompanied by enhancement of tolerance against various stress stimuli, such as osmotic stress, ethanol, hydrogen peroxide, high temperature and freezing. Unlike bacterial ppGpp accumulation, ppGpp was accumulated in the early growth phase but not in the late growth phase. Moreover, nutritional downshift resulted in a decrease in ppGpp level, suggesting that the observed Sj-RSH activity to synthesize ppGpp is not starvation-dependent, contrary to our expectations based on bacteria. Accumulated ppGpp was found to be present solely in the cytosolic fraction and not in the mitochondrial fraction, perhaps reflecting the ribosome-independent ppGpp synthesis in S. cerevisiae cells. Unlike bacterial inosine monophosphate (IMP) dehydrogenases, the IMP dehydrogenase of S. cerevisiae was insensitive to ppGpp. Microarray analysis showed that ppGpp accumulation gave rise to marked changes in gene expression, with both upregulation and downregulation, including changes in mitochondrial gene expression. The most prominent upregulation (38-fold) was detected in the hypothetical gene YBR072C-A of unknown function, followed by many other known stress-responsive genes. S. cerevisiae may provide new opportunities to uncover and analyse the ppGpp signalling system in eukaryotic cells.
引用
收藏
页码:2213 / 2224
页数:12
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