Effect of nutrient starvation on the cellular composition and metabolic capacity of Saccharomyces cerevisiae

被引:39
作者
Albers, Eva
Larsson, Christer
Andlid, Thomas
Walsh, Michael C.
Gustafsson, Lena
机构
[1] Chalmers, Dept Chem & Biol Engn Mol Biotechnol, SE-40530 Gothenburg, Sweden
[2] Chalmers, Dept Chem & Biol Engn Food Sci, SE-41296 Gothenburg, Sweden
[3] Heineken Tech Serv, NL-2382 PH Zoeterwoude, Netherlands
关键词
D O I
10.1128/AEM.00425-07
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 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
This investigation addresses the following question: what are the important factors for maintenance of a high catabolic capacity under various starvation conditions? Saccharomyces cerevisiae was cultured in aerobic batch cultures, and during the diauxic shift cells were transferred and subjected to 24 h of starvation. The following conditions were used: carbon starvation, nitrogen starvation in the presence of glucose or ethanol, and both carbon starvation and nitrogen starvation. During the starvation period changes in biomass composition (including protein, carbohydrate, lipid, and nucleic acid contents), metabolic activity, sugar transport kinetics, and the levels of selected enzymes were recorded. Subsequent to the starvation period the remaining catabolic capacity was measured by addition of 50 mM glucose. The results showed that the glucose transport capacity is a key factor for maintenance of high metabolic capacity in many, but not all, cases. The results for cells starved of carbon, carbon and nitrogen, or nitrogen in the presence of glucose all indicated that the metabolic capacity was indeed controlled by the glucose transport ability, perhaps with some influence of hexokinase, phosphofructokinase, aldolase, and enolase levels. However, it was also demonstrated that there was no such correlation when nitrogen starvation occurred in the presence of ethanol instead of glucose.
引用
收藏
页码:4839 / 4848
页数:10
相关论文
共 56 条
[1]
Influence of the nitrogen source on Saccharomyces cerevisiae anaerobic growth and product formation [J].
Albers, E ;
Larsson, C ;
Liden, G ;
Niklasson, C ;
Gustafsson, L .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (09) :3187-3195
[2]
Ser3p (Yer081wp) and Ser33p (Yil074cp) are phosphoglycerate dehydrogenases in Saccharomyces cerevisiae [J].
Albers, E ;
Laizé, V ;
Blomberg, A ;
Hohmann, S ;
Gustafsson, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (12) :10264-10272
[3]
ANDLID T, 1995, APPL MICROBIOL BIOT, V42, P818
[4]
A SIMPLE AND RELIABLE METHOD FOR THE DETERMINATION OF CELLULAR RNA-CONTENT [J].
BENTHIN, S ;
NIELSEN, J ;
VILLADSEN, J .
BIOTECHNOLOGY TECHNIQUES, 1991, 5 (01) :39-42
[5]
BRUINENBERG PM, 1983, J GEN MICROBIOL, V129, P965
[6]
BUSTURIA A, 1986, J GEN MICROBIOL, V132, P379
[7]
REGULATION OF CARBON METABOLISM IN CHEMOSTAT CULTURES OF SACCHAROMYCES-CEREVISIAE GROWN ON MIXTURES OF GLUCOSE AND ETHANOL [J].
DEJONGGUBBELS, P ;
VANROLLEGHEM, P ;
HEIJNEN, S ;
VANDIJKEN, JP ;
PRONK, JT .
YEAST, 1995, 11 (05) :407-418
[8]
Strategies to determine the extent of control exerted by glucose transport on glycolytic flux in the yeast Saccharomyces bayanus [J].
Diderich, JA ;
Teusink, B ;
Valkier, J ;
Anjos, J ;
Spencer-Martins, I ;
van Dam, K ;
Walsh, MC .
MICROBIOLOGY-SGM, 1999, 145 :3447-3454
[9]
DRYER RL, 1957, J BIOL CHEM, V225, P177
[10]
Transcriptional responses to glucose at different glycolytic rates in Saccharomyces cerevisiae [J].
Elbing, K ;
Ståhlberg, A ;
Hohmann, S ;
Gustafsson, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2004, 271 (23-24) :4855-4864