Systems biology approach reveals that overflow metabolism of acetate in Escherichia coli is triggered by carbon catabolite repression of acetyl-CoA synthetase

被引:178
作者
Valgepea, Kaspar [1 ,2 ]
Adamberg, Kaarel [2 ,3 ]
Nahku, Ranno [1 ,2 ]
Lahtvee, Petri-Jaan [1 ,2 ]
Arike, Liisa [2 ,3 ]
Vilu, Raivo [1 ,2 ]
机构
[1] Tallinn Univ Technol, Dept Chem, EE-12618 Tallinn, Estonia
[2] Competence Ctr Food & Fermentat Technol, EE-12618 Tallinn, Estonia
[3] Tallinn Univ Technol, Food Proc Dept, EE-19086 Tallinn, Estonia
关键词
LIMITED CONTINUOUS-CULTURE; GLOBAL GENE-EXPRESSION; CHEY PHOSPHORYLATION; DENSITY GROWTH; ACKA-PTA; A-STAT; GLUCOSE; PHOSPHATE; PROTEIN; FLUX;
D O I
10.1186/1752-0509-4-166
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The biotechnology industry has extensively exploited Escherichia coli for producing recombinant proteins, biofuels etc. However, high growth rate aerobic E. coli cultivations are accompanied by acetate excretion i.e. overflow metabolism which is harmful as it inhibits growth, diverts valuable carbon from biomass formation and is detrimental for target product synthesis. Although overflow metabolism has been studied for decades, its regulation mechanisms still remain unclear. Results: In the current work, growth rate dependent acetate overflow metabolism of E. coli was continuously monitored using advanced continuous cultivation methods (A-stat and D-stat). The first step in acetate overflow switch (at mu = 0.27 +/- 0.02 h(-1)) is the repression of acetyl-CoA synthethase (Acs) activity triggered by carbon catabolite repression resulting in decreased assimilation of acetate produced by phosphotransacetylase (Pta), and disruption of the PTA-ACS node. This was indicated by acetate synthesis pathways PTA-ACKA and POXB component expression down-regulation before the overflow switch at mu = 0.27 +/- 0.02 h(-1) with concurrent 5-fold stronger repression of acetate-consuming Acs. This in turn suggests insufficient Acs activity for consuming all the acetate produced by Pta, leading to disruption of the acetate cycling process in PTA-ACS node where constant acetyl phosphate or acetate regeneration is essential for E. coli chemotaxis, proteolysis, pathogenesis etc. regulation. In addition, two-substrate A-stat and D-stat experiments showed that acetate consumption capability of E. coli decreased drastically, just as Acs expression, before the start of overflow metabolism. The second step in overflow switch is the sharp decline in cAMP production at mu = 0.45 h(-1) leading to total Acs inhibition and fast accumulation of acetate. Conclusion: This study is an example of how a systems biology approach allowed to propose a new regulation mechanism for overflow metabolism in E. coli shown by proteomic, transcriptomic and metabolomic levels coupled to two-phase acetate accumulation: acetate overflow metabolism in E. coli is triggered by Acs down-regulation resulting in decreased assimilation of acetic acid produced by Pta, and disruption of the PTA-ACS node.
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页数:13
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共 59 条
[1]   Pyruvate oxidase contributes to the aerobic growth efficiency of Escherichia coli [J].
Abdel-Hamid, AM ;
Attwood, MM ;
Guest, JR .
MICROBIOLOGY-SGM, 2001, 147 :1483-1498
[2]   Quasi steady state growth of Lactococcus lactis in glucose-limited acceleration stat (A-stat) cultures [J].
Adamberg, Kaarel ;
Lahtvee, Petri-Jaan ;
Valgepea, Kaspar ;
Abner, Kristo ;
Vilu, Raivo .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2009, 95 (03) :219-226
[3]   Uropathogenic Escherichia coli CFT073 Is Adapted to Acetatogenic Growth but Does Not Require Acetate during Murine Urinary Tract Infection [J].
Anfora, Andrew T. ;
Halladin, David K. ;
Haugen, Brian J. ;
Welch, Rodney A. .
INFECTION AND IMMUNITY, 2008, 76 (12) :5760-5767
[4]   Both acetate kinase and acetyl coenzyme A synthetase are involved in acetate-stimulated change in the direction of flagellar rotation in Escherichia coli [J].
Barak, R ;
Abouhamad, WN ;
Eisenbach, M .
JOURNAL OF BACTERIOLOGY, 1998, 180 (04) :985-988
[5]   ACETYLADENYLATE OR ITS DERIVATIVE ACETYLATES THE CHEMOTAXIS PROTEIN CHEY INVITRO AND INCREASES ITS ACTIVITY AT THE FLAGELLAR SWITCH [J].
BARAK, R ;
WELCH, M ;
YANOVSKY, A ;
OOSAWA, K ;
EISENBACH, M .
BIOCHEMISTRY, 1992, 31 (41) :10099-10107
[6]   PRIDE Converter: making proteomics data-sharing easy [J].
Barsnes, Harald ;
Vizcaino, Juan Antonio ;
Eidhammer, Ingvar ;
Martens, Lennart .
NATURE BIOTECHNOLOGY, 2009, 27 (07) :598-599
[7]   An insight into the role of phosphotransacetylase (pta) and the acetate/acetyl-CoA node in Escherichia coli [J].
Castano-Cerezo, Sara ;
Pastor, Jose M. ;
Renilla, Sergio ;
Bernal, Vicente ;
Iborra, Jose L. ;
Canovas, Manuel .
MICROBIAL CELL FACTORIES, 2009, 8
[8]   Biofuel production in Escherichia coli: the role of metabolic engineering and synthetic biology [J].
Clomburg, James M. ;
Gonzalez, Ramon .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2010, 86 (02) :419-434
[9]   Effects of mutations in acetate metabolism on high-cell-density growth of Escherichia coli [J].
Contiero, J ;
Beatty, C ;
Kumari, S ;
DeSanti, CL ;
Strohl, WR ;
Wolfe, A .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2000, 24 (06) :421-430
[10]   Kinetics of CheY phosphorylation by small molecule phosphodonors [J].
Da Re, SS ;
Deville-Bonne, D ;
Tolstykh, T ;
Véron, M ;
Stock, JB .
FEBS LETTERS, 1999, 457 (03) :323-326