Keyword search (4,163 papers available)

"Martin VJ" Authored Publications:

Title Authors PubMed ID
1 Global view of the Clostridium thermocellum cellulosome revealed by quantitative proteomic analysis. Gold ND, Martin VJ 17644599
BIOLOGY
2 Proteomic analysis of Clostridium thermocellum ATCC 27405 reveals the upregulation of an alternative transhydrogenase-malate pathway and nitrogen assimilation in cells grown on cellulose. Burton E, Martin VJ 23210995
BIOLOGY
3 Expression of a library of fungal β-glucosidases in Saccharomyces cerevisiae for the development of a biomass fermenting strain. Wilde C, Gold ND, Bawa N, Tambor JH, Mougharbel L, Storms R, Martin VJ 22218767
CSFG
4 Effects of synthetic cohesin-containing scaffold protein architecture on binding dockerin-enzyme fusions on the surface of Lactococcus lactis. Wieczorek AS, Martin VJ 23241215
CSFG
5 Reconstitution of a 10-gene pathway for synthesis of the plant alkaloid dihydrosanguinarine in Saccharomyces cerevisiae. Fossati E, Ekins A, Narcross L, Zhu Y, Falgueyret JP, Beaudoin GA, Facchini PJ, Martin VJ 24513861
BIOLOGY
6 Deconstructing the genetic basis of spent sulphite liquor tolerance using deep sequencing of genome-shuffled yeast. Pinel D, Colatriano D, Jiang H, Lee H, Martin VJ 25866561
CSFG
7 Synthesis of Morphinan Alkaloids in Saccharomyces cerevisiae. Fossati E, Narcross L, Ekins A, Falgueyret JP, Martin VJ 25905794
BIOLOGY
8 An enzyme-coupled biosensor enables (S)-reticuline production in yeast from glucose. DeLoache WC, Russ ZN, Narcross L, Gonzales AM, Martin VJ, Dueber JE 25984720
BIOLOGY
9 Metabolic engineering of a tyrosine-overproducing yeast platform using targeted metabolomics. Gold ND, Gowen CM, Lussier FX, Cautha SC, Mahadevan R, Martin VJ 26016674
CSFG
10 Directed evolution of a fungal β-glucosidase in Saccharomyces cerevisiae. Larue K, Melgar M, Martin VJ 26949413
CSFG
11 Engineering of a Nepetalactol-Producing Platform Strain of Saccharomyces cerevisiae for the Production of Plant Seco-Iridoids. Campbell A, Bauchart P, Gold ND, Zhu Y, De Luca V, Martin VJ 26981892
CSFG
12 Seamless site-directed mutagenesis of the Saccharomyces cerevisiae genome using CRISPR-Cas9. Biot-Pelletier D, Martin VJ 27134651
BIOLOGY
13 Reconstituting Plant Secondary Metabolism in Saccharomyces cerevisiae for Production of High-Value Benzylisoquinoline Alkaloids. Pyne ME, Narcross L, Fossati E, Bourgeois L, Burton E, Gold ND, Martin VJ 27417930
CSFG
14 Mining Enzyme Diversity of Transcriptome Libraries through DNA Synthesis for Benzylisoquinoline Alkaloid Pathway Optimization in Yeast. Narcross L, Bourgeois L, Fossati E, Burton E, Martin VJ 27442619
BIOLOGY
15 Persistence of Escherichia coli in batch and continuous vermicomposting systems. Hénault-Ethier L, Martin VJ, Gélinas Y 27499290
BIOLOGY

 

Title:Reconstituting Plant Secondary Metabolism in Saccharomyces cerevisiae for Production of High-Value Benzylisoquinoline Alkaloids.
Authors:Pyne MENarcross LFossati EBourgeois LBurton EGold NDMartin VJ
Link:https://www.ncbi.nlm.nih.gov/pubmed/27417930?dopt=Abstract
DOI:10.1016/bs.mie.2016.02.011
Publication:Methods in enzymology
Keywords:AlkaloidsBenzylisoquinoline alkaloidsMetabolic engineeringOpiatesSaccharomyces cerevisiaeSecondary metabolismSynthetic biologyYeast
PMID:27417930 Category:Methods Enzymol Date Added:2019-06-07
Dept Affiliation: CSFG
1 Centre for Structural and Functional Genomics, Concordia University, Montréal, QC, Canada.
2 Centre for Structural and Functional Genomics, Concordia University, Montréal, QC, Canada. Electronic address: vincent.martin@concordia.ca.

Description:

Reconstituting Plant Secondary Metabolism in Saccharomyces cerevisiae for Production of High-Value Benzylisoquinoline Alkaloids.

Methods Enzymol. 2016;575:195-224

Authors: Pyne ME, Narcross L, Fossati E, Bourgeois L, Burton E, Gold ND, Martin VJ

Abstract

Benzylisoquinoline alkaloids (BIAs) constitute a diverse class of plant secondary metabolites that includes the opiate analgesics morphine and codeine. Collectively, BIAs exhibit a myriad of pharmacological activities, including antimicrobial, antitussive, antispasmodic, and anticancer properties. Despite 2500 known BIA products, only a small proportion are currently produced though traditional crop-based manufacturing, as complex stereochemistry renders chemical synthesis of BIAs largely unfeasible. The advent of synthetic biology and sophisticated microbial engineering coupled with recent advances in the elucidation of plant BIA metabolic networks has provided growing motivation for producing high-value BIAs in microbial hosts. Here, we provide a technical basis for reconstituting BIA biosynthetic pathways in the common yeast Saccharomyces cerevisiae. Methodologies outlined in this chapter include fundamental techniques for expressing and assaying BIA biosynthetic enzymes, bioprospecting large libraries of BIA enzyme variants, and reconstituting and optimizing complete BIA formation pathways in yeast. To expedite construction of superior BIA-producing yeast strains, we emphasize high-throughput techniques. Finally, we identify fundamental challenges impeding deployment of yeast-based BIA production platforms and briefly outline future prospects to overcome such barriers.

PMID: 27417930 [PubMed - indexed for MEDLINE]





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