Results 31 to 40 of about 15,660 (211)

Solution structure of the type I polyketide synthase Pks13 from Mycobacterium tuberculosis

open access: yesBMC Biology, 2022
Background Type I polyketide synthases (PKSs) are multifunctional enzymes responsible for the biosynthesis of a group of diverse natural compounds with biotechnological and pharmaceutical interest called polyketides.
Cécile Bon   +14 more
doaj   +1 more source

The role of the phosphopantetheinyltransferase enzyme, PswP, in the biosynthesis of antimicrobial secondary metabolites by Serratia marcescens Db10 [PDF]

open access: yes, 2014
Phosphopantetheinyltransferase (PPTase) enzymes fulfil essential roles in primary and secondary metabolism in prokaryotes, archaea and eukaryotes. PPTase enzymes catalyse the essential modification of the carrier protein domain of fatty acid synthases ...
Amy J. Gerc   +9 more
core   +4 more sources

Module-Based Polyketide Synthase Engineering for de Novo Polyketide Biosynthesis [PDF]

open access: yesACS Synthetic Biology, 2023
Polyketide retrobiosynthesis, where the biosynthetic pathway of a given polyketide can be reversibly engineered due to the colinearity of the polyketide synthase (PKS) structure and function, has the potential to produce millions of organic molecules. Mixing and matching modules from natural PKSs is one of the routes to produce many of these molecules.
Alberto A. Nava   +4 more
openaire   +4 more sources

Expanding the Utility of Bioinformatic Data for the Full Stereostructural Assignments of Marinolides A and B, 24- and 26-Membered Macrolactones Produced by a Chemically Exceptional Marine-Derived Bacterium

open access: yesMarine Drugs, 2023
Marinolides A and B, two new 24- and 26-membered bacterial macrolactones, were isolated from the marine-derived actinobacterium AJS-327 and their stereostructures initially assigned by bioinformatic data analysis.
Min Cheol Kim   +4 more
doaj   +1 more source

Mining microbial genomes for new natural products and biosynthetic pathways [PDF]

open access: yes, 2008
Analyses of microbial genome sequences have revealed numerous examples of ‘cryptic’ or ‘orphan’ biosynthetic gene clusters, with the potential to direct the production of novel, structurally complex natural products.
Austin   +67 more
core   +2 more sources

A single amino acid residue controls acyltransferase activity in a polyketide synthase from Toxoplasma gondii

open access: yesiScience, 2022
Summary: Type I polyketide synthases (PKSs) are multidomain, multimodule enzymes capable of producing complex polyketide metabolites. These modules contain an acyltransferase (AT) domain, which selects acyl-CoA substrates to be incorporated into the ...
Hannah K. D’Ambrosio   +3 more
doaj   +1 more source

Isolation of pigment cell specific genes in the sea urchin embryo by differential macroarray screening [PDF]

open access: yes, 2003
New secondary mesenchyme specific genes, expressed exclusively in pigment cells, were isolated from sea urchin embryos using a differential screening of a macroarray cDNA library. The comparison was performed between mRNA populations of embryos having an
Calestani, Cristina   +2 more
core   +1 more source

Identification of a putative polyketide synthase gene involved in usnic acid biosynthesis in the lichen Nephromopsis pallescens.

open access: yesPLoS ONE, 2018
Usnic acid is a unique polyketide produced by lichens. To characterize usnic acid biosynthesis, the transcriptome of the usnic-acid-producing lichen-forming fungus Nephromopsis pallescens was sequenced using Illumina NextSeq technology.
Yi Wang   +5 more
doaj   +1 more source

Expansion and Conservation of Biosynthetic Gene Clusters in Pathogenic Pyrenophora spp.

open access: yesToxins, 2020
Pyrenophora is a fungal genus responsible for a number of major cereal diseases. Although fungi produce many specialised or secondary metabolites for defence and interacting with the surrounding environment, the repertoire of specialised metabolites (SM)
Paula M. Moolhuijzen   +6 more
doaj   +1 more source

Suzuki–Miyaura Reaction in the Presence of N-Acetylcysteamine Thioesters Enables Rapid Synthesis of Biomimetic Polyketide Thioester Surrogates for Biosynthetic Studies

open access: yesChemistry, 2023
Biomimetic N-acetylcysteamine thioesters are essential for the study of polyketide synthases, non-ribosomal peptide synthetases and fatty acid synthases.
Sebastian Derra   +2 more
doaj   +1 more source

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