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Gene Review

ackA  -  acetate kinase

Escherichia coli CFT073

 
 
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Disease relevance of ackA

  • The Bacillus subtilis gene encoding acetate kinase was identified on the basis of sequence similarity to the Escherichia coli ackA gene and to a second E. coli gene closely related to ackA [1].
  • Our laboratory previously studied the interaction between nuo and the acetate-producing pathway encoded by ackA-pta in Escherichia coli [2].
  • Recent work in this laboratory has shown that the gene coding for acetate kinase (ackA) in Sinorhizobium meliloti is up-regulated in response to phosphate limitation [3].
 

High impact information on ackA

  • Indeed, the ability to synthesize acetyl phosphate, an intermediate of the pathway, appears to be indispensable for glucose-starved cells as pta and pta-ackA double mutants were found to be impaired in their ability to survive glucose starvation [4].
  • We propose that cells regulate intracellular acetyl phosphate concentrations relative to growth phase and temperature by modulating the availability of acetyl-CoA, the expression of ackA, and the activity of phosphotransacetylase [5].
  • We isolated insertions in ackA and pta, which comprise a two-gene operon responsible for the acetate<-->acetyl coenzyme A interconversion [6].
  • An ackA mutant, lacking the ability to generate ATP from acetyl phosphate, also failed to grow in xylose minimal medium under anaerobic conditions, confirming the need for the ATP produced by acetate kinase for anaerobic growth on xylose [7].
  • Since arabinose transport by AraE, the low-affinity, high-capacity, arabinose/H+ symport, conserves the ATP expended in pentose transport by the ABC transporter, both pfl and ackA mutants grew anaerobically with arabinose [7].
 

Biological context of ackA

 

Associations of ackA with chemical compounds

  • A similar benefit was obtained by inactivation of acetate kinase (ackA), reducing the production of acetate (and ATP) and sparing acetyl-CoA for biosynthetic needs [11].
  • The ackA-pta mutant has a pfl::lacZ expression level much higher than that of the wild-type strain, and cultures also exhibit the highest ethanol production [2].
  • The cell yield and lactate productivity were increased by a further mutation in the acetate kinase gene (ackA) [12].
  • Earlier we have shown that acetate pathway deletion (ackA-pta) increases isoamyl acetate production [13].

References

  1. Regulation of the Bacillus subtilis acetate kinase gene by CcpA. Grundy, F.J., Waters, D.A., Allen, S.H., Henkin, T.M. J. Bacteriol. (1993) [Pubmed]
  2. Expression of the pfl gene and resulting metabolite flux distribution in nuo and ackA-pta E. coli mutant strains. Singh, R., Yang, Y.T., Lu, B., Bennett, G.N., San, K.Y. Biotechnol. Prog. (2006) [Pubmed]
  3. Genes coding for phosphotransacetylase and acetate kinase in Sinorhizobium meliloti are in an operon that is inducible by phosphate stress and controlled by phoB. Summers, M.L., Denton, M.C., McDermott, T.R. J. Bacteriol. (1999) [Pubmed]
  4. The glucose-starvation stimulon of Escherichia coli: induced and repressed synthesis of enzymes of central metabolic pathways and role of acetyl phosphate in gene expression and starvation survival. Nyström, T. Mol. Microbiol. (1994) [Pubmed]
  5. Regulation of acetyl phosphate synthesis and degradation, and the control of flagellar expression in Escherichia coli. Prüss, B.M., Wolfe, A.J. Mol. Microbiol. (1994) [Pubmed]
  6. A defect in the acetyl coenzyme A<-->acetate pathway poisons recombinational repair-deficient mutants of Escherichia coli. Shi, I.Y., Stansbury, J., Kuzminov, A. J. Bacteriol. (2005) [Pubmed]
  7. Pyruvate formate lyase and acetate kinase are essential for anaerobic growth of Escherichia coli on xylose. Hasona, A., Kim, Y., Healy, F.G., Ingram, L.O., Shanmugam, K.T. J. Bacteriol. (2004) [Pubmed]
  8. Overproduction of acetate kinase activates the phosphate regulon in the absence of the phoR and phoM functions in Escherichia coli. Lee, T.Y., Makino, K., Shinagawa, H., Nakata, A. J. Bacteriol. (1990) [Pubmed]
  9. Cloning of a gene coding for phosphotransacetylase from Escherichia coli. Yamamoto-Otake, H., Matsuyama, A., Nakano, E. Appl. Microbiol. Biotechnol. (1990) [Pubmed]
  10. Paired termini stabilize antisense RNAs and enhance conditional gene silencing in Escherichia coli. Nakashima, N., Tamura, T., Good, L. Nucleic Acids Res. (2006) [Pubmed]
  11. Genetic changes to optimize carbon partitioning between ethanol and biosynthesis in ethanologenic Escherichia coli. Underwood, S.A., Zhou, S., Causey, T.B., Yomano, L.P., Shanmugam, K.T., Ingram, L.O. Appl. Environ. Microbiol. (2002) [Pubmed]
  12. Production of optically pure D-lactic acid in mineral salts medium by metabolically engineered Escherichia coli W3110. Zhou, S., Causey, T.B., Hasona, A., Shanmugam, K.T., Ingram, L.O. Appl. Environ. Microbiol. (2003) [Pubmed]
  13. Applicability of CoA/acetyl-CoA manipulation system to enhance isoamyl acetate production in Escherichia coli. Vadali, R.V., Bennett, G.N., San, K.Y. Metab. Eng. (2004) [Pubmed]
 
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