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| Home > Publications database > Mutational analysis and reconstituted expression of the biosynthetic genes involved in the formation of 3-amino-5-hydroxybenzoic acid : the starter unit of rifamycin biosynthesis in Amycolatopsis mediterranei S699 |
| Home > Publications database > Mutational analysis and reconstituted expression of the biosynthetic genes involved in the formation of 3-amino-5-hydroxybenzoic acid : the starter unit of rifamycin biosynthesis in Amycolatopsis mediterranei S699 |
| Journal Article | PreJuSER-33246 |
; ; ;
2001
Soc.
Bethesda, Md.
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Please use a persistent id in citations: http://hdl.handle.net/2128/2835 doi:10.1074/jbc.M009667200
Abstract: To investigate a novel branch of the shikimate biosynthesis pathway operating in the formation of 3-amino-5-hydroxybenzoic acid (AHBA), the unique biosynthetic precursor of rifamycin and related ansamycins, a series of target-directed mutations and heterologous gene expressions were investigated in Amycolatopsis mediterranei and Streptomyces coelicolor. The genes involved in AHBA formation were inactivated individually, and the resulting mutants were further examined by incubating the cell-free extracts with known intermediates of the pathway and analyzing for AHBA formation. The rifL, -M, and -N genes were shown to be involved in the step(s) from either phosphoenolpyruvate/d-erythrose 4-phosphate or other precursors to 3,4-dideoxy-4-amino-d-arabino-heptulosonate 7-phosphate. The gene products of the rifH, -G, and -J genes resemble enzymes involved in the shikimate biosynthesis pathway (August, P. R., Tang, L., Yoon, Y. J., Ning, S., Müller, R., Yu, T.-W., Taylor, M., Hoffmann, D., Kim, C.-G., Zhang, X., Hutchinson, C. R., and Floss, H. G. (1998) Chem. Biol. 5, 69-79). Mutants of the rifH and -J genes produced rifamycin B at 1% and 10%, respectively, of the yields of the wild type; inactivation of the rifG gene did not affect rifamycin production significantly. Finally, coexpressing the rifG-N and -J genes in S. coelicolor YU105 under the control of the act promoter led to significant production of AHBA in the fermented cultures, confirming that seven of these genes are indeed necessary and sufficient for AHBA formation. The effects of deletion of individual genes from the heterologous expression cassette on AHBA formation duplicated the effects of the genomic rifG-N and -J mutations on rifamycin production, indicating that all these genes encode proteins with catalytic rather than regulatory functions in AHBA formation for rifamycin biosynthesis by A. mediterranei.
Keyword(s): Actinomycetales: enzymology (MeSH) ; Actinomycetales: genetics (MeSH) ; Amino Acid Sequence (MeSH) ; Aminobenzoic Acids: metabolism (MeSH) ; Base Sequence (MeSH) ; DNA Mutational Analysis: methods (MeSH) ; DNA Primers (MeSH) ; Genes, Bacterial (MeSH) ; Genes, Regulator (MeSH) ; Molecular Sequence Data (MeSH) ; Multigene Family (MeSH) ; Open Reading Frames (MeSH) ; Plasmids (MeSH) ; Promoter Regions, Genetic (MeSH) ; Restriction Mapping (MeSH) ; Rifabutin: metabolism (MeSH) ; Rifamycins: biosynthesis (MeSH) ; Aminobenzoic Acids ; DNA Primers ; Rifamycins ; Rifabutin ; 3-amino-5-hydroxybenzoic acid ; J
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