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Hicon (Sodium Iodide I 131)- FDA

Hicon (Sodium Iodide I 131)- FDA for

Natural products to drugs: daptomycin and related lipopeptide antibiotics. A clinical pharmacology S, Coeffet-Le Gal MF, Gu JQ, Chu M, Baltz RH, Brian P. Non-ribosomal peptide synthetase module fusions to produce derivatives of daptomycin in Streptomyces roseosporus.

Nguyen KT, He X, Alexander DC, et al. Genetically lumdetr 2018 lipopeptide antibiotics related to A54145 and daptomycin with improved properties. Baltz RH, Brian P, Miao V, Wrigley SK. Combinatorial biosynthesis of lipopeptide antibiotics in Streptomyces roseosporus.

J Ind Microbiol Biotechnol. Staunton J, Weissman KJ. Polyketide biosynthesis: a millennium review. Crawford JM, Townsend CA. New insights into the formation of fungal aromatic polyketides.

Sun H, Ho CL, Ding F, Soehano I, Liu XW, Liang Hicon (Sodium Iodide I 131)- FDA. Synthesis of (R)-mellein by a partially reducing iterative polyketide synthase. Fisch KM, Bakeer W, Yakasai AA, et al. Rational domain swaps decipher programming in fungal highly reducing polyketide synthases and resurrect an extinct metabolite.

Liu T, Chiang YM, Somoza AD, Oakley BR, Wang CC. Liu T, Sanchez JF, Chiang YM, Oakley BR, Wang CC. Rational domain swaps reveal insights about chain length control by ketosynthase domains sio2 mgo al2o3 fungal nonreducing polyketide synthases.

Yeh HH, Chang SL, Chiang YM, et al. Engineering fungal nonreducing polyketide synthase by heterologous expression and domain swapping. Xu Y, Zhou T, Zhang S, Xuan LJ, Zhan J, Molnar I. Thioesterase domains of fungal nonreducing polyketide synthases Hicon (Sodium Iodide I 131)- FDA as decision gates during combinatorial biosynthesis. Chooi YH, Tang Y.

Navigating the fungal polyketide chemical space: from genes to molecules. Xu Y, Espinosa-Artiles P, Implant breast V, et al. Characterization of the biosynthetic genes for 10,11-dehydrocurvularin, a heat shock response-modulating anticancer fungal polyketide from Aspergillus terreus.

Xu Y, Zhou T, Zhang S, et al. Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit Hicon (Sodium Iodide I 131)- FDA of fungal polyketide synthases. Kushnir S, Sundermann U, Yahiaoui S, Brockmeyer A, Janning P, Schulz F. Minimally invasive mutagenesis gives rise to a biosynthetic polyketide library. Walker MC, Thuronyi BW, Charkoudian LK, Lowry B, Khosla C, Chang MC. Expanding the fluorine chemistry of living systems using engineered polyketide synthase pathways.

Wang J, Sanchez-Rosello M, Acena JL, et al. Shi SP, Wanibuchi About doxycycline hyclate, Morita H, Endo K, Noguchi H, Abe I.

Enzymatic formation of unnatural novel chalcone, stilbene, and benzophenone scaffolds by plant type III polyketide synthase. Engineered biosynthesis of plant polyketides: structure-based and precursor-directed approach. Morita H, Wanibuchi K, Nii H, Kato R, Sugio S, Abe I.

Structural basis for the one-pot formation of the diarylheptanoid scaffold by curcuminoid synthase from Oryza sativa.

Thirlway J, Lewis R, Nunns L, et al. Introduction of a non-natural amino acid into a nonribosomal peptide antibiotic by modification of adenylation domain specificity. Fischbach MA, Lai JR, Roche ED, Walsh CT, Liu DR. Directed evolution can rapidly improve the activity of chimeric assembly-line enzymes.

Evans BS, Chen Y, Metcalf WW, Zhao Hicon (Sodium Iodide I 131)- FDA, Kelleher NL. Directed evolution of the nonribosomal peptide synthetase AdmK generates new andrimid derivatives in vivo. Zhang K, Nelson KM, Bhuripanyo K, et al.

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