Pregled bibliografske jedinice broj: 87067
Genetic methods for the manipulation of polyketide-producing actinomycetes
Genetic methods for the manipulation of polyketide-producing actinomycetes // Program and Abstracts / Kniewald, Zlatko et al. (ur.).
Zagreb: Hrvatsko Društvo za Biotehnologiju, 2001. str. 21 (IL-13) (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 87067 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetic methods for the manipulation of polyketide-producing actinomycetes
Autori
Cullum, John ; Hranueli, Daslav ; Lal, Rup ; Padilla, Gabriel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Program and Abstracts
/ Kniewald, Zlatko et al. - Zagreb : Hrvatsko Društvo za Biotehnologiju, 2001, 21 (IL-13)
Skup
Biotechnology and Environment Scientific Conference with International Participation
Mjesto i datum
Zagreb, Hrvatska, 19.02.2001. - 21.02.2001
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Polyketides; actinomycetes; biosynthetic clusters; genetic manipulation
Sažetak
Polyketides produced by actinomycetes are of great industrial importance (e.g. avermectin from Streptomyces avermitilis, oxytetracycline from Streptomyces rimosus, rifamycin from Amycolatopsis mediterranei). Some polyketide synthetases are of the Type I modular form (e.g. avermectin, rifamycin) in which each extension step is mediated by its own module. In Type II polyketide synthetases (e.g. oxytetracycline) the enzyme is used iteratively. In both cases, genetic manipulation of the biosynthetic clusters can produce novel polyketides. Because of the large size of the clusters (typically 30-150 kb) this is usually achieved by introducing constructs made by in vitro genetics into the clusters by homologous recombination. Many industrially important strains give problems for genetic manipulation including low transformation frequencies, the possession of methylation-dependent restriction systems, the failure of common cloning vectors to replicate in the strain, resistance to antibiotics commonly used in cloning vectors and the occurrence of genetic instability. Instead of protoplast transformation it is possible to use electroporation or conjugation from E. coli to introduce DNA into some species. One strategy to select the required recombination events is the use of counterselectable markers and linear plasmid vectors should be useful in future.
Izvorni jezik
Engleski
Znanstvena područja
Prehrambena tehnologija
POVEZANOST RADA
Projekti:
058407
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb
Profili:
Daslav Hranueli
(autor)