
We thank Fermentek for the information, the free Nonactin granted for our project, and most of all, the moral support |
Link friends 17dmag 7aad actinomycin alfatoxin-b1 aflatoxin-b2 aflatoxin-g1 aflatoxin-g2 aflatoxin-m1 aflatoxin-m2 anisomycin ascomycin Blukher Bukharin dybenko frinovsky geldanamycin k252a k252b kt5720 kt5823 leptomycin Link-Exchange mithramycin mitomycin nonactin Ochratoxin parthenolide Snorring staurosporine tinnitus trichostatin tukhachevsky verruculogen vomitoxin wortmannin yakir yegorov yezhov zearalenone
Here come some links to top-rated hrefs, such as Microsoft, wikipedia, Google and Yahoo :google, microsoft, yahoo, wikipedia
Now come links to these of fermentek product pages, that are needy : .the homepage of fermentek, FK506 or tacrolimus, products of Fermentek: staurosporine, K252A, aflatoxin, Sirolimus (Rapamycin) And other link beggars: Tinnitus. about some guys that had tinnitus | 7: J Am Chem Soc. 2002 Mar 27;124(12):2894-902. Nonactin biosynthesis: the initial committed step is the condensation of acetate (malonate) and succinate.
Nelson ME, Priestley ND.
Department of Chemistry, The University of Montana, Missoula, MT 59812-1656, USA.
Nonactin is a macrotetrolide antibiotic produced by Streptomyces griseus subsp. griseus ETH A7796 that has shown activity against the P170-glycoprotein efflux pump associated with multiple drug resistant cancer cells. Nonactin is a polyketide, albeit a highly atypical one. The structure is composed of two units of each of the enantiomers of nonactic acid, arranged in a macrocycle, so that the molecule has S4 symmetry and is achiral. The monomer units, (+)- and (-)-nonactic acid, are derived from acetate, succinate, and propionate, although the exact details of the assembly process are quite unclear. We have used feeding experiments with a series of multiple stable isotope labeled precursors to elucidate the details of the first committed step of nonactic acid biosynthesis. We have found that the (13)C label from 3-ketoadipate is incorporated specifically into both nonactic acid and its homologue, homononactic acid. The data conclusively show that the first committed step of nonactin biosynthesis is the coupling of a succinate derivative with either acetate or malonate. The differentiation into either nonactate or homononactate occurs after the initial condensation; the homologues are not derived from use of a different "starter unit" by the nonactate polyketide synthase. The first step of nonactin biosynthesis involves achiral intermediates; differentiation between the known enantiocomplementary biosynthesis pathways to form each enantiomer of the precursor monomer units likely occurs after the initial condensation reaction. |
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