Literature DB >> 9260959

A novel alternate anaplerotic pathway to the glyoxylate cycle in streptomycetes.

L Han1, K A Reynolds.   

Abstract

ccr encoding crotonyl coenzyme A (CoA) reductase (CCR), which catalyzes the conversion of crotonyl-CoA to butyryl-CoA in the presence of NADPH, was previously cloned from Streptomyces collinus. We now report that a complete open reading frame, designated meaA, is located downstream from ccr. The predicted gene product showed 35% identity with methylmalonyl-CoA mutases from various sources. In addition, the predicted amino acid sequences of S. collinus ccr and meaA exhibit strong similarity to that of adhA (43% identity), a putative alcohol dehydrogenase gene, and meaA (62% identity) of Methylobacterium extorquens, respectively. Both adhA and meaA are involved in the assimilation of C1 and C2 compounds in an unknown pathway in the isocitrate lyase (ICL)-negative Methylobacterium. We have demonstrated that S. collinus can grow with acetate as its sole carbon source even though there is no detectable ICL, suggesting that in this organism ccr and meaA may also be involved in a pathway for the assimilation of C2 compounds. Previous studies with streptomycetes provided a precedent for a pathway that initiates with the condensation of two acetyl-CoA molecules to form butyryl-CoA, which is then transformed to succinyl-CoA with two separate CoB12-mediated rearrangements and a series of oxidations. The biological functions of ccr and meaA in this process were investigated by gene disruption. A ccr-blocked mutant showed no detectable crotonyl-CoA reductase activity and, compared to the wild-type strain, exhibited dramatically reduced growth when acetate was the sole carbon source. An meaA-blocked mutant also exhibited reduced growth on acetate. However, both methylmalonyl-CoA mutase and isobutyryl-CoA mutase, which catalyze the two CoB12-dependent rearrangements in this proposed pathway, were shown to be present in the meaA-blocked mutant. These results suggested that both ccr and meaA are involved in a novel pathway for the growth of S. collinus when acetate is its sole carbon source.

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Year:  1997        PMID: 9260959      PMCID: PMC179375          DOI: 10.1128/jb.179.16.5157-5164.1997

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  27 in total

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Journal:  Biochem J       Date:  1986-06-01       Impact factor: 3.857

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Journal:  Nature       Date:  1983 Sep 22-28       Impact factor: 49.962

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8.  Molecular characterization of a chromosomal region involved in the oxidation of acetyl-CoA to glyoxylate in the isocitrate-lyase-negative methylotroph Methylobacterium extorquens AM1.

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Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

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  25 in total

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Journal:  J Bacteriol       Date:  2003-05       Impact factor: 3.490

2.  Identification of genes involved in the glyoxylate regeneration cycle in Methylobacterium extorquens AM1, including two new genes, meaC and meaD.

Authors:  Natalia Korotkova; Mary E Lidstrom; Ludmila Chistoserdova
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Review 3.  Biosynthesis of polyketide synthase extender units.

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Journal:  Biotechnol Biofuels       Date:  2016-02-24       Impact factor: 6.040

5.  Genetic Plasticity and Ethylmalonyl Coenzyme A Pathway during Acetate Assimilation in Rhodospirillum rubrum S1H under Photoheterotrophic Conditions.

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6.  Identification and disruptional analysis of the Streptomyces cinnamonensis msdA gene, encoding methylmalonic acid semialdehyde dehydrogenase.

Authors:  Chaoxuan Li; Konstantin Akopiants; Kevin A Reynolds
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7.  Multiple pathways for acetate assimilation in Streptomyces cinnamonensis.

Authors:  Konstantin Akopiants; Galina Florova; Chaoxuan Li; Kevin A Reynolds
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8.  Role of crotonyl coenzyme A reductase in determining the ratio of polyketides monensin A and monensin B produced by Streptomyces cinnamonensis.

Authors:  H Liu; K A Reynolds
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

9.  Connection between poly-beta-hydroxybutyrate biosynthesis and growth on C(1) and C(2) compounds in the methylotroph Methylobacterium extorquens AM1.

Authors:  N Korotkova; M E Lidstrom
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10.  The ethylmalonyl-CoA pathway is used in place of the glyoxylate cycle by Methylobacterium extorquens AM1 during growth on acetate.

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