Pregled bibliografske jedinice broj: 197712
Ablation of a post-polyketide hydroxylase from the oxytetracyline biosynthetic pathway results in novel polyketides with altered chain length
Ablation of a post-polyketide hydroxylase from the oxytetracyline biosynthetic pathway results in novel polyketides with altered chain length // The Chemistry and Biology of Natural Product Biosynthesis II
Bristol: Royal Society of Chemistry, U.K., 2005. (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 197712 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Ablation of a post-polyketide hydroxylase from the oxytetracyline biosynthetic pathway results in novel polyketides with altered chain length
Autori
Perić-Concha, Nataša
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
The Chemistry and Biology of Natural Product Biosynthesis II
/ - Bristol : Royal Society of Chemistry, U.K., 2005
Skup
The Chemistry and Biology of Natural Product Biosynthesis II
Mjesto i datum
Bristol, Ujedinjeno Kraljevstvo, 15.06.2005
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Streptomyces rimosus; oxytetracycline; otcC gene; C-6-hydroylase; novel polyketides
Sažetak
Oxytetracycline (OTC), a polyketide antibiotic, is made by Streptomyces rimosus through the sequential condensation of eight acetate units to a three-carbon starter unit. The otcC gene encodes a C-6-hydroylase that is involved in the late stages of biosynthesis after the polyketide backbone is completed. A recombinant, which was disrupted in the genomic copy of otcC, synthesized at least three novel polyketides of shorter chain lengths (17 and 16 carbons) than OTC (19 carbons). No compound containing a full-length chain was detected in the recombinant culture. This result indicates that the absence of the otcC gene product has a significant effect on the ability of the OTC ‘ minimal PKS’ to make a polyketide product of the usual chain length. A mutant copy of otcC was made by site-directed mutagenesis of three essential glycine codons located within the putative NADPH-binding domain. Expression of the mutant gene in E. coli confirmed that this gene product was catalytically-inactive. When the mutant gene replaced the ablated gene in the chromosome of S. rimosus, the ability to make a 19-carbon backbone was restored, indicating that OtcC is an essential structural partner in the quaternary structure of the synthase complex.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija