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Article Abstract

Natural acylsucrose, often found in the glandular trichomes of plants, has potential applications in many industries, including food, cosmetics, and pharmaceuticals. In this study, we engineered an strain to complete the biosynthesis of acylsucroses through whole-cell transformation. Using acylsucrose acyltransferases and CoA ligases, acylsucroses, including monoacylsucrose S1:5 ("S" represents an acylsucrose backbone, the number before the colon indicates the number of acyl chains, and the number after the colon indicates the sum of carbons in all acyl chains), diacylsucrose S2:10, triacylsucrose S3:14, and triacylsucrose S3:15 were synthesized from the substrate sucrose and short branched-chain fatty acids by the engineered EcoSE07, of which S3:15 was the primary product. Several strategies were applied to improve acylsucrose production, including codon optimization, constitutive promoter replacement, and serial resting cell assays. The use of fed-batch fermentation with an engineered strain of EcoSE22 containing a constitutive promoter further improved the production of acylsucroses. Serial resting cell assays with an optical density of 50 at 600 nm significantly increased the production of acylsucroses S3:15 and S2:10. These findings will facilitate the synthesis of natural acylsucroses through whole-cell transformations and provide the potential for future industrial applications.

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http://dx.doi.org/10.1021/acs.jafc.5c00568DOI Listing

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Natural acylsucrose, often found in the glandular trichomes of plants, has potential applications in many industries, including food, cosmetics, and pharmaceuticals. In this study, we engineered an strain to complete the biosynthesis of acylsucroses through whole-cell transformation. Using acylsucrose acyltransferases and CoA ligases, acylsucroses, including monoacylsucrose S1:5 ("S" represents an acylsucrose backbone, the number before the colon indicates the number of acyl chains, and the number after the colon indicates the sum of carbons in all acyl chains), diacylsucrose S2:10, triacylsucrose S3:14, and triacylsucrose S3:15 were synthesized from the substrate sucrose and short branched-chain fatty acids by the engineered EcoSE07, of which S3:15 was the primary product.

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Acylsugars are polyesters of short- to medium-length acyl chains on sucrose or glucose backbones that are produced in secretory glandular trichomes of many solanaceous plants, including cultivated tomato (Solanum lycopersicum). Despite their roles in biotic stress adaptation and their wide taxonomic distribution, there is relatively little information about the diversity of these compounds and the genes responsible for their biosynthesis. In this study, acylsugar diversity was assessed for 80 accessions of the wild tomato species Solanum habrochaites from throughout the Andes Mountains.

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Structure elucidation of acylsucrose derivatives from Atractylodes lanceae rhizome and Atractylodes rhizome.

Nat Prod Commun

August 2009

Division of Pharmacognosy, Department of Medicinal Resources, Institute of Natural Medicine, University of Toyama, Sugitani, Toyama, Japan.

The mass chromatographic fingerprints of the water extracts of Atractylodes rhizome and Atractylodes lancea rhizome were analyzed by LC-MS. Three new acylsucrose derivatives [2,6,3',6'-tetra(3-methylbutanoyl)sucrose (1), 2,4,3',6'-tetra(3-methylbutanoyl)sucrose (2), and a mixture of 3',4',6'-tris(3-methylbutanoyl)-1'-(2-methylbutanoyl)sucrose and 1',3',4',6'-tetra(3-methylbutanoyl)sucrose (6)), along with three known acylsucroses (2,6,3',4'-tetra(3-methylbutanoyl)sucrose (3), 2,4,3',4'-tetra(3-methylbutanoyl)sucrose (4) and a mixture of 2,3',6'-tris(3-methylbutanoyl)-1'-(2-methylbutanoyl)sucrose and 2,1',3',6'-tetra(3-methylbutanoyl)sucrose (5)] were isolated as the marker compounds of Atractylodes rhizome and Atractylodes lancea rhizome. The structures of the compounds were elucidated by MS/MS analyses and NMR experiments.

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