Name | acetyl CoA synthetase |
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Synonyms | ACAS 2; ACS; MYH7B; Acetyl Coenzyme A synthetase 2; ACAS2; ACSA; ACSS 2; ACSS2… |
Name | TCA |
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CAS | 2,2,2-trichloroacetic acid |
PubMed | Abstract | RScore(About this table) | |
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19861411 | Jensen PR, Peitersen T, Karlsson M, In 't Zandt R, Gisselsson A, Hansson G, Meier S, Lerche MH: Tissue-specific short chain fatty acid metabolism and slow metabolic recovery after ischemia from hyperpolarized NMR in vivo. J Biol Chem. 2009 Dec 25;284(52):36077-82. Epub 2009 Oct 27. This is achieved by assaying acetyl-CoA synthetase and acetyl- transferase catalyzed transformations in vivo. |
2(0,0,0,2) | Details |
16310273 | Li M, Ho PY, Yao S, Shimizu K: Effect of lpdA gene knockout on the metabolism in Escherichia coli based on enzyme activities, intracellular metabolite concentrations and metabolic flux analysis by 13C-labeling experiments. J Biotechnol. 2006 Mar 23;122(2):254-66. Epub 2005 Nov 23. Based on the investigation of enzyme activities and intracellular metabolite concentrations, was considered to be formed by the combined reactions through oxidase (PoxB), acetyl-CoA synthetase (Acs) and kinase (Ack)-phosphoacetyltransferase (Pta) in the lpdA mutant. |
1(0,0,0,1) | Details |
16551598 | Wen L, Liu G, Zhang ZJ, Tao J, Wan CX, Zhu YG: [Preliminary proteomics analysis of the total proteins of HL Type cytoplasmic male sterility rice anther]. Yi Chuan. 2006 Mar;28(3):311-6. Among those proteins, there were Putative nucleic acid binding protein, adenylyltransferase (ADP- pyrophosphorylase, AGPase) (EC: 2.7.7.27) large chain, UDP- decarboxylase, putative -binding protein annexin, putative acetyl-CoA synthetase and putative dehydrogenase etc. |
3(0,0,0,3) | Details |
15063611 | Phue JN, Shiloach J: Transcription levels of key metabolic genes are the cause for different In addition, there is a difference between the two strains in the transcription of the acetyl-CoA synthetase (acs), phosphotransacetylase- kinase (pta-ackA) pathway, and oxidase (poxB), pathway. |
utilization pathways in E. coli B (BL21) and E. coli K (JM109). J Biotechnol. 2004 Apr 8;109(1-2):21-30.1(0,0,0,1) | Details |
15806547 | Phue JN, Noronha SB, Hattacharyya R, Wolfe AJ, Shiloach J: In a series of previous reports it was established by implementing metabolic flux, NMR/MS, and Northern blot analysis that the shunt, the TCA cycle, and uptake by acetyl-CoA synthetase are more active in Escherichia coli BL21 than in Escherichia coli JM109. |
metabolism at high density growth of E. coli B and E. coli K: differences in metabolic pathways are responsible for efficient utilization in E. coli B as determined by microarrays and Northern blot analyses. Biotechnol Bioeng. 2005 Jun 30;90(7):805-20.1(0,0,0,1) | Details |
16209543 | Wang Y, Wu SL, Hancock WS, Trala R, Kessler M, Taylor AH, Patel PS, Aon JC: Proteomic profiling of Escherichia coli proteins under high cell density fed-batch cultivation with overexpression of phosphogluconolactonase. Biotechnol Prog. 2005 Sep-Oct;21(5):1401-11. During the time course of samples collected during the rapid growth achieved under batch and fed-batch conditions, both the control and recombinant E. coli strains showed up-regulation of proteins participating in the tricarboxylic acid (TCA) cycle, particularly acetyl-CoA synthetase (AcCoAS), malate dehydrogenase (MDH), and synthetase (SuccCoAS). |
1(0,0,0,1) | Details |