Biosynthesis of Colabomycin E, a New Manumycin-Family Metabolite, Involves an Unusual Chain-Length Factor

0434468 - MBÚ 2015 RIV DE eng J - Článek v odborném periodiku
Petříčková, Kateřina - Pospíšil, Stanislav - Kuzma, Marek - Tylová, Tereza - Jágr, Michal - Tomek, P. - Chroňáková, Alica - Brabcová, E. - Anděra, Ladislav - Krištůfek, Václav - Petříček, Miroslav
Biosynthesis of Colabomycin E, a New Manumycin-Family Metabolite, Involves an Unusual Chain-Length Factor.
Chembiochem. Roč. 15, č. 9 (2014), s. 1334-1345. ISSN 1439-4227. E-ISSN 1439-7633
Grant CEP: GA MZd(CZ) NT13012
Institucionální podpora: RVO:61388971 ; RVO:60077344 ; RVO:68378050
Klíčová slova: biosynthesis * chain-length factors * manumycins
Kód oboru RIV: CE - Biochemie
Impakt faktor: 3.088, rok: 2014

Colabomycin E is a new member of the manumycin-type metabolites produced by the strain Streptomyces aureus SOK1/5-04 and identified by genetic screening from a library of streptomycete strains. The structures of colabomycin E and accompanying congeners were resolved. The entire biosynthetic gene cluster was cloned and expressed in Streptomyces lividans. Bioinformatic analysis and mutagenic studies identified components of the biosynthetic pathway that are involved in the formation of both polyketide chains. Recombinant polyketide synthases (PKSs) assembled from the components of colabomycin E and asukamycin biosynthetic routes catalyzing the biosynthesis of "lower" carbon chains were constructed and expressed in S. aureus SOK1/5-04 Delta colC11-14 deletion mutant. Analysis of the metabolites produced by recombinant strains provided evidence that in both biosynthetic pathways the length of the lower carbon chain is controlled by an unusual chain-length factor supporting biosynthesis either of a triketide in asukamycin or of a tetraketide in colabomycin E. Biological activity assays indicated that colabomycin E significantly inhibited IL-1 beta release from THP-1 cells and might thus potentially act as an anti-inflammatory agent
Trvalý link: http://hdl.handle.net/11104/0238536