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Polyketid synthases

Role of polyketide synthases in biosynthesis of some heterocycles, in particular macrolides 97CRV2465. [Pg.238]

It is very likely that a similar Type I polyketide synthase constructs the naphthoate fragment of azinomycin B. This will be a very interesting enzyme to study, since it will need to perform an unprecedented three regioselective reduction reactions, as well as controlling the polyketide chain length and directing its cycliza-tion. [Pg.427]

The biosynthesis of maduropeptin has not been studied in detail, but an iterative type I polyketide synthase gene predicted to be responsible for forming the enediyne core structure has been identified [188]. [Pg.433]

Hutchinson, R.C., Microbial polyketide synthases more and more prolific, Proc. Natl. Acad. Sci. USA, 96, 3336, 1999. [Pg.119]

Kim, J.E. et ah. Putative polyketide synthase and laccase for biosynthesis of auro-fusarin in Gibberella zea, Appl. Environ. Microbiol., 71, 1701, 2005. [Pg.119]

Will it be possible to use individual dehydrogenase modules from large assemblies such as polyketide synthases ... [Pg.295]

B. Nowak-Thompson, S. J. Gould, and J. E. Loper, Identification and sequence analysis of the genes encoding a polyketide synthase required for pyoluteorin biosynthesis in Pseudomonas fluorescens Pf-5. Gene (1997). [Pg.221]

It was proposed that a Diels-Alder cyclization occurred during a polyketide synthase assembly of the bicyclic core of Lovastatin by Aspergillus terreus MF 4845." In vitro Diels-Alder cyclization of the corresponding model compounds generated two analogous diastere-omers in each case, under either thermal or Lewis-acid-catalyzed conditions (Eq. 12.37). As expected, the Diels-Alder reaction occurred faster in aqueous media. The cyclization half-life in chloroform at room temperature is 10 days while in aqueous media at either pH 5 or 7, the half-life drops to two days. [Pg.398]

Hutchinson, C.R. and Fujii, I. (1995) Polyketide synthase gene manipulation a structure-function approach in engineering novel antibiotics. Annual Review of Microbiology, 49, 201. [Pg.257]

Khosla, C. (1997) Harnessing the biosynthetic potential of modular polyketide synthases. Chemical Reviews, 97, 2577. [Pg.257]

Shen, B. (2003) Polyketide biosynthesis beyond the type I, II and III polyketide synthase paradigms. Current Opinion in Chemical Biology, 7, 285. [Pg.257]

Jenke-Kodama, H., Sandmann, A., Muller, R. and Dittmann, E. (2005) Evolutionary implications of bacterial polyketide synthases. Molecular Biology and Evolution, 22, 2027. [Pg.257]

Liu, W., Nonaka, K., Nie, L. et al. (2005) The neocarzinostatin biosynthetic gene cluster from Streptomyces carzinostaticus ATCC 15944 involving two iterative type I polyketide synthases. Chemistry Biology, 12, 293. [Pg.258]

Liu, W., Ahlert, J., Gao, Q. et al. (2003) Rapid PCR amplification of minimal enediyne polyketide synthase cassettes leads to a predictive familial classification model. Proceedings of the National Academy of Sciences of the United States of America, 100, 11959. [Pg.258]

Long, P.F., Wilkinson, C.J., Bisang, C.P. et al. (2002) Engineering specificity of starter unit selection by the erythromycin-producing polyketide synthase. Molecular Microbiology, 43, 1215. [Pg.258]

Marsden, A.F., Wilkinson, B., Cortes, J. et al. (1998) Engineering broader specificity into an antibiotic-producing polyketide synthase. Science, 279, 199. [Pg.258]

Petkovic, H., Lill, R.E., Sheridan, R.M. et al. (2003) A novel erythromycin, 6-desmethyl erythromycin D, made by substituting an acyltransferase domain of the erythromycin polyketide synthase. The Journal of Antibiotics, 56, 543. [Pg.258]

Ruan, X., Pereda, A., Stassi, D.L. et al. (1997) Acyltransferase domain substitutions in erythromycin polyketide synthase yield novel erythromycin derivatives. Journal of Bacteriology, 179, 6416. [Pg.258]

Del Vecchio, F., Petkovic, H., Kendrew, S.G. et al. (2003) Active-site residue, domain and module swaps in modular polyketide synthases. Journal of Industrial Microbiology Biotechnology, 30, 489. [Pg.258]

Reeves, C.D., Murli, S., Ashley, G.W. et al. (2001) Alteration of the substrate specificity of a modular polyketide synthase acyltransferase domain through site-specific mutations. Biochemistry, 40, 15464. [Pg.258]

Kumar, P., Koppisch, A.T., Cane, D.E. and Khosla, C. (2003) Enhancing the modularity ofthe modular polyketide synthases transacylation in modular polyketide synthases catalyzed by malonyl-CoA ACPtransacylase. Journal of the American Chemical Society, 125, 14307. [Pg.258]

Kao, C.M., Luo, G.L., Katz, L. et al. (1995) Engineered biosynthesis of a triketide lactone from an incomplete modular polyketide synthase. Journal of the American Chemical Society, 117, 9105. [Pg.259]

Roberts, G.A., Staunton, J. and Leadlay, P.F. (1993) Heterologous expression in Escherichia coli of an intact multienzyme component of the erythromycin-producing polyketide synthase. European Journal of Biochemistry, 214, 305. [Pg.259]

The biosynthesis of polyketides (including chain initiation, elongation, and termination processes) is catalyzed by large multi-enzyme complexes called polyketide synthases (PKSs). The polyketides are synthesized from starter units such as acetyl-CoA, propionyl-CoA, and other acyl-CoA units. Extender units such as malonyl-CoA and methylmalonyl-CoA are repetitively added via a decarboxylative process to a growing carbon chain. Ultimately, the polyketide chain is released from the PKS by cleavage of the thioester, usually accompanied by chain cyclization [49]. [Pg.268]

Pohl, N.L. (2002) Nonnatural substrates for polyketide synthases and their associated modifying enzymes. Current Opinion in Chemical Biology, 6, 773-778. [Pg.283]

Yoon, Y.J., Beck, B.J., Kim, B.S. et al. (2002) Generation of multiple bioactive macrolides by hybrid modular polyketide synthases in Streptomyces venezuelae. Chemistry Biology, 9, 203-214. [Pg.283]

Menzella, H.G., Reid, R., Carney, J.R. et al. (2005) Combinatorial polyketide biosynthesis by de novo design and rearrangement of modular polyketide synthase genes. Nature Biotechnology, 23, 1171-1176. [Pg.283]

Ward, S.L., Desai, R.P., Hu, Z. et al. (2007) Precursor-directed biosynthesis of 6-deoxyerythronolide B analogues is improved by removal of the initial catalytic sites of the polyketide synthase. Journal of Industrial Microbiology and Biotechnology, 34, 9-15. [Pg.283]

Cane, D.E. and Walsh, C.T. (1999) The parallel and convergent universes of polyketide synthases and nonribosomal peptide synthetases. Chemistry Biology, 6 (12), R319—R325. [Pg.315]

Moore, B.S. and Hertweck, C. (2002) Biosynthesis and attachment of novel bacterial polyketide synthase starter units. Natural Product Reports, 19 (1), 70-99. [Pg.315]

MacNeil, D.J., Occi, J.L., Gewain, K.M. et al. (1992) Complex organization of the Streptomyces avermetilis genes encoding the avermectin polyketide synthase. Gene, 115, 119-125. [Pg.316]

Lu, H., Tsai, S.-C., Khosla, C. and Cane, D.E. (2002) Expression, site-directed mutagenesis, and steady state kinetic analysis of the terminal thioesterase domain of the methymycin/picromycin polyketide synthase. Biochemistry, 41, 12590-12597. [Pg.316]


See other pages where Polyketid synthases is mentioned: [Pg.355]    [Pg.425]    [Pg.426]    [Pg.427]    [Pg.430]    [Pg.488]    [Pg.102]    [Pg.299]    [Pg.11]    [Pg.247]    [Pg.259]    [Pg.315]   
See also in sourсe #XX -- [ Pg.150 , Pg.151 ]




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