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Ikeda H, Ishikawa J, Hanamoto A, Shinose M, Kikuchi H, Shiba T, Sakaki Y, Hattori M, Omura S (2003) Complete genome sequence and comparative assessment of the industrial microorganism Streptomyces avermitilis. Olano C, Rodriguez AM, Michel JM, Mendez C, Raynal MC, Salas JA (1998) Analysis of a Streptomyces antibioticus chromosomal location associated in oleandomycin biosynthesis, which encodes two glycosyltransferases responsible for glycosylation of the macrolactone ring. Madduri K, Kennedy J, Rivola G, Inventi-Solari A, Filippini S, Zanuso G, Colombo AL, Gewain KM, Occi JL, MacNeil DJ, Hutchinson CR (1998) Production of the antitumor drug epirubicin (4′-epidoxorubicin) and its precursor by a genetically engineered pressure of Streptomyces peucetius. Wohlert S, Lomovskaya N, Kulowski K, Fonstein L, Occi JL, Gewain KM, MacNeil DJ, Hutchinson CR (2001) Insights about the biosynthesis of the avermectin deoxysugar L-oleandrose by way of heterologous expression of Streptomyces avermitilis deoxysugar genes in Streptomyces lividans. 2002) The cytochrome P450 complement (CYPome) of Streptomyces coelicolor A3(2). Podust LM, Kim Y, Arase M, Neely BA, Beck BJ, Bach H, Sherman DH, Lamb DC, Kelly SL, Waterman MR (2003) The 1.92-A composition of Streptomyces coelicolor A3(2) CYP154C1.
Lamb DC, Skaug T, Song HL, Jackson CJ, Podust LM, Waterman MR, Kell DB, Kelly DE, Kelly SL. Jacobsen JR, Hutchinson CR, Cane DE, Khosla C (1997) Precursor directed biosynthesis of novel erythromycin analogs by an engineered polyketide synthase. Khosla C, Gokhale R, Jacobsen JR, Cane DE (1999) Tolerance and specificity of polyketide synthases. Henkel T, Brunne RM, Müller H (1999) Statistical investigation into the structural complementarity of all-natural products and synthetic compounds. Schwarzer D, Marahiel MA (2001) Multimodular biocatalysts for organic item assembly. Khosla C (2000) Natural products biosynthesis: A new interface among en-zymology and drugs. Staunton J, Weissman KJ (2001) Polyketide biosynthesis: a millennium evaluate. Tang L, McDaniel R (2001) Construction of desosamine that contains polyketide libraries utilizing a glycosyltransferase with wide substrate specificity. Hutchinson CR, McDaniel R (2001) Combinatorial biosynthesis in microorganisms as a route to new antimicrobial, antitumor and neuroregenerative prescription drugs. Staunton J, Wilkinson B (2001) Combinatorial biosynthesis of polyketides and nonribosomal peptides. Trefzer A, Blanco G, Remsing L, Künzel E, Rix U, Lipata F, Brana AF, Mendez C, Rohr J, Bechthold A, Salas JA (2002b) Rationally created glycosylated premithramycins: hybrid aromatic polyketides utilizing genes from a few various biosynthetic pathways. Patallo EP, Blanco G, Fischer C, Brana AF, Rohr J, Mendez C, Salas JA (2001) Deoxysugar methylation for the duration of biosynthesis of the antitumor polyketide elloramycin by Streptomyces olivaceus.
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Hoffmeister D, Drager G, Ichinose K, Rohr J, Bechthold A (2003) The C-glycosyltransferase UrdGT2 is unselective toward D-and L-configured nucleotide-bound rhodinoses. Metsä-Ketelä M, Palmu K, Kunnari T, Ylihonko K, Mantsälä P (2003) Engineering anthracycline biosynthesis towards angucyclines. Shen B, Du L, Sanchez C, Chen M, Edwards DJ (1999) Bleomycin biosynthesis in Streptomyces verticillus ATCC 15003: a product of hybrid peptide and polyketide biosynthesis. Walsh CT (2002) Combinatorial biosynthesis of antibiotics: difficulties and alternatives. Waugh ACW, Long PF (2002) Prospects for creating new antibiotics. Onaka H, Taniguchi S, Igarashi Y, Furumai T (2002) Cloning of the staurosporine biosynthetic gene cluster from Streptomyces sp. Ruan X, Stassi D, Lax SA, Katz L (1997) A second style-I PKS gene cluster isolated from Streptomyces hygroscopicus ATCC 29253, a rapamycin-creating strain. Strohl WR (1997) Industrial Antibiotics: right now and the future. Zähner H, Fiedler HP (1995) The want for new antibiotics: Possible approaches ahead. But, at the time you visit the hookup sites, you will have to have to pay at some issue as the cost-free versions of these web sites tend to be confined. Given its concentration on as well as-dimension singles, you could possibly discover that you are far more limited in phrases of assortment than with other websites.
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