Differential glucose repression in common yeast strains in response to HXK2 deletion

被引:49
作者
Kummel, Anne [1 ]
Ewald, Jennifer Christina [1 ,2 ,3 ]
Fendt, Sarah-Maria [1 ,2 ,3 ]
Jol, Stefan Jasper [1 ,3 ]
Picotti, Paola [1 ]
Aebersold, Ruedi [1 ,2 ,4 ,5 ]
Sauer, Uwe [1 ,2 ]
Zamboni, Nicola [1 ,2 ]
Heinemann, Matthias [1 ,2 ,6 ]
机构
[1] ETH, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
[2] Competence Ctr Syst Physiol & Metab Dis, Zurich, Switzerland
[3] Life Sci Zurich PhD Program Syst Biol Complex Dis, Zurich, Switzerland
[4] Inst Syst Biol, Seattle, WA USA
[5] Univ Zurich, Fac Sci, Zurich, Switzerland
[6] Univ Groningen, Groningen Biomol Sci & Biotechnol Inst, Groningen, Netherlands
关键词
glucose repression; hexokinase; 2; FY4; CEN; PK; PKA; metabolomics; SACCHAROMYCES-CEREVISIAE STRAINS; METABOLIC FLUX ANALYSIS; PROTEIN-KINASE-A; CATABOLITE REPRESSION; CYCLIC-AMP; NUCLEAR-LOCALIZATION; ADENYLATE-CYCLASE; GENE DISRUPTION; HEXOKINASE PII; PHOSPHORYLATION;
D O I
10.1111/j.1567-1364.2010.00609.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Under aerobic, high glucose conditions, Saccharomyces cerevisiae exhibits glucose repression and thus a predominantly fermentative metabolism. Here, we show that two commonly used prototrophic representatives of the CEN.PK and S288C strain families respond differently to deletion of the hexokinase 2 (HXK2) - a key player in glucose repression: In CEN.PK, growth rate collapses and derepression occurs on the physiological level, while the S288C descendant FY4 delta hxk2 still grows like the parent strain and shows a fully repressed metabolism. A CEN.PK delta hxk2 strain with a repaired adenylate cyclase gene CYR1 maintains repression but not growth rate. A comparison of the parent strain's physiology, metabolome, and proteome revealed higher metabolic rates, identical biomass, and byproduct yields, suggesting a lower Snf1 activity and a higher protein kinase A (PKA) activity in CEN.PK. This study highlights the importance of the genetic background in the processes of glucose signaling and regulation, contributes novel evidence on the overlap between the classical glucose repression pathway and the cAMP/PKA signaling pathway, and might have the potential to resolve some of the conflicting findings existing in the field.
引用
收藏
页码:322 / 332
页数:11
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