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Establishing a toolkit for precursor-directed polyketide biosynthesis: exploring substrate promiscuities of acid-CoA ligases
- Source :
- Biochemistry. 51(22)
- Publication Year :
- 2012
-
Abstract
- Polyketides are chemically diverse and medicinally important biochemicals that are biosynthesized from acyl-CoA precursors by polyketide synthases. One of the limitations to combinatorial biosynthesis of polyketides has been the lack of a toolkit that describes the means of delivering novel acyl-CoA precursors necessary for polyketide biosynthesis. Using five acid-CoA ligases obtained from various plants and microorganisms, we biosynthesized an initial library of 79 acyl-CoA thioesters by screening each of the acid-CoA ligases against a library of 123 carboxylic acids. The library of acyl-CoA thioesters includes derivatives of cinnamyl-CoA, 3-phenylpropanoyl-CoA, benzoyl-CoA, phenylacetyl-CoA, malonyl-CoA, saturated and unsaturated aliphatic CoA thioesters, and bicyclic aromatic CoA thioesters. In our search for the biosynthetic routes of novel acyl-CoA precursors, we discovered two previously unreported malonyl-CoA derivatives (3-thiophenemalonyl-CoA and phenylmalonyl-CoA) that cannot be produced by canonical malonyl-CoA synthetases. This report highlights the utility and importance of determining substrate promiscuities beyond conventional substrate pools and describes novel enzymatic routes for the establishment of precursor-directed combinatorial polyketide biosynthesis.
- Subjects :
- Models, Molecular
Stereochemistry
Carboxylic Acids
Polyketide biosynthesis
Streptomyces coelicolor
Biology
Biochemistry
Substrate Specificity
Polyketide
Bacterial Proteins
Coenzyme A Ligases
Cloning, Molecular
Bacteria
food and beverages
Esters
Oryza
respiratory system
Substrate (biology)
Plants
carbohydrates (lipids)
Polyketides
lipids (amino acids, peptides, and proteins)
Acyl Coenzyme A
human activities
Polyketide Synthases
Rhizobium
Subjects
Details
- ISSN :
- 15204995
- Volume :
- 51
- Issue :
- 22
- Database :
- OpenAIRE
- Journal :
- Biochemistry
- Accession number :
- edsair.doi.dedup.....4a13f1c551d7baee20be445d7e322265