about
Behind enemy lines.Orthogonal ligation: a three piece assembly of a PNA-peptide-PNA conjugate.Heterologous expression of the oxytetracycline biosynthetic pathway in Myxococcus xanthus.Land use intensity controls actinobacterial community structureTotal biosynthesis of antitumor nonribosomal peptides in Escherichia coli.Alternative sigma factor over-expression enables heterologous expression of a type II polyketide biosynthetic pathway in Escherichia coli.The role of transcription in heterologous expression of polyketides in bacterial hosts.Bioinformatics tools for genome mining of polyketide and non-ribosomal peptides.Inducible T7 RNA Polymerase-mediated Multigene Expression System, pMGX.Sampling Terrestrial Environments for Bacterial Polyketides.Draft Genome Sequence of Streptomyces sp. Strain PBH53, Isolated from an Urban Environment.Biosynthesis of ebelactone A: isotopic tracer, advanced precursor and genetic studies reveal a thioesterase-independent cyclization to give a polyketide β-lactone.Atropselective macrocyclization of diaryl ether ring systems: application to the synthesis of vancomycin model systems.Examining the role of hydrogen bonding interactions in the substrate specificity for the loading step of polyketide synthase thioesterase domains.Epothilone C macrolactonization and hydrolysis are catalyzed by the isolated thioesterase domain of epothilone polyketide synthase.Understanding substrate specificity of polyketide synthase modules by generating hybrid multimodular synthases.Biomimetic transannular oxa-conjugate addition approach to the 2,6-disubstituted dihydropyran of laulimalide yields an unprecedented transannular oxetane.A new mechanism for benzopyrone formation in aromatic polyketide biosynthesis.Precursor-directed biosynthesis of epothilone in Escherichia coli.Total Biosynthesis of Legionaminic Acid, a Bacterial Sialic Acid Analogue.Natural products: Mapping an amazing thicket.Does CIP Nomenclature Adequately Handle Molecules with Multiple Stereoelements? A Case Study of Vancomycin and Cognates We would like to thank Professor Dieter Hellwinkel for pointing out to us the stereochemical discrepancies in our review6 and elsSialic acid and N-acyl sialic acid analog production by fermentation of metabolically and genetically engineered Escherichia coli.The thioesterase domain from the pimaricin and erythromycin biosynthetic pathways can catalyze hydrolysis of simple thioester substrates.Polyketide synthase thioesterases catalyze rapid hydrolysis of peptidyl thioesters6-Deoxyerythronolide B synthase thioesterase-catalyzed macrocyclization is highly stereoselectiveReinvestigation of coenzyme Q10 isolation from Sporidiobolus johnsoniiNon-canonical regioisomerizations and a 'Diels-Alderase' are likely essential in the biosynthesis of spiculoic acid AAn evolutionary model encompassing substrate specificity and reactivity of type I polyketide synthase thioesterasesChemoenzymatic macrocycle synthesis using resorcylic acid lactone thioesterase domainsThioesterase from Cereulide Biosynthesis Is Responsible for Oligomerization and Macrocyclization of a Linear Tetradepsipeptide
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Christopher N Boddy
@ast
Christopher N Boddy
@en
Christopher N Boddy
@es
Christopher N Boddy
@nl
Christopher N Boddy
@sl
type
label
Christopher N Boddy
@ast
Christopher N Boddy
@en
Christopher N Boddy
@es
Christopher N Boddy
@nl
Christopher N Boddy
@sl
prefLabel
Christopher N Boddy
@ast
Christopher N Boddy
@en
Christopher N Boddy
@es
Christopher N Boddy
@nl
Christopher N Boddy
@sl
P106
P21
P31
P496
0000-0002-3259-3184