Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Drug
Enzyme
Compound
Query: EC:6.2.1.13 (
acetyl-CoA synthetase
)
451
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The time, yield and related genes expression of
PHB
accumulation of Acidiphilium cryptum DX1-1 were investigated under four different initial C/N ratios 1.2, 2.4, 7.5, and 24. The results of time and yield of
PHB
accumulation show that the initial C/N ratio 2.4 was optimum for strain DX1-1 to accumulate
PHB
, both higher and lower initial C/N ratios did not favor that process. Based on the genome of Acidiphilium cryptum JF-5, 13
PHB
accumulation related genes in strain JF-5 were chosen and successfully cloned from strain DX1-1. The differential expression of the 13 functional genes, in different C/N ratios as cited above, was then studied by Real-time PCR. The results show that all the 13 genes were most upregulated when initial C/N ratio was 2.4, and among which the gene Acry_3030 encoding poly-beta-hydroxybutyrate polymerase and Acry_0626 encoding
acetyl-CoA synthetase
were much more upregulated than the other genes, which prove that they play the most important role for
PHB
accumulation and acetate is the main initial substance for
PHB
accumulation for strain DX1-1. Potential regulatory motifs analysis shows that the genes related to
PHB
accumulation are regulated by different promoters and that the motif had weak similarity to the model promoters, suggesting that
PHB
- metabolism in Acidiphilium cryptum may be mediated by a different mechanism.
...
PMID:Real-time PCR analysis of metabolic pathway of PHB in Acidiphilium cryptum DX1-1. 2013 35
Poly(3-hydroxybutyrate) (
PHB
) is a biodegradable and biocompatible thermoplastic, and synthesized from the central metabolite acetyl-CoA. The acetyl-CoA synthesis from glucose presents low atomic economy due to the release of CO
2
in pyruvate decarboxylation. As ethanol and acetate can be converted into acetyl-CoA directly, they were used as carbon source for
PHB
production in this study. The reductase mutant AdhE A267T/E568K was introduced into
Escherichia coli
to enable growth on ethanol, and acetate utilization was improved by overexpression of
acetyl-CoA synthetase
ACS. Comparison of the
PHB
production using glucose, ethanol or acetate as sole carbon source showed that the production and yield from ethanol was much higher than those from glucose and acetate, and metabolome analysis revealed the differences in metabolism of glucose, ethanol and acetate. Furthermore, other acetyl-CoA derived chemicals including 3-hydroxypropionate and phloroglucinol were produced from those three feedstocks, and similar results were achieved, suggesting that ethanol could be a suitable carbon source for the production of acetyl-CoA derivatives.
...
PMID:Comparison of Glucose, Acetate and Ethanol as Carbon Resource for Production of Poly(3-Hydroxybutyrate) and Other Acetyl-CoA Derivatives. 3285 Jul 13