about
The genome sequence of E. coli W (ATCC 9637): comparative genome analysis and an improved genome-scale reconstruction of E. coliIsoprene synthesis protects transgenic tobacco plants from oxidative stressMolecular control of sucrose utilization in Escherichia coli W, an efficient sucrose-utilizing strainDual gene expression cassette vectors with antibiotic selection markers for engineering in Saccharomyces cerevisiae.Circadian control of isoprene emissions from oil palm (Elaeis guineensis).2,2-Diphenyl-1-picrylhydrazyl as a screening tool for recombinant monoterpene biosynthesis.The trehalose phosphotransferase system (PTS) in E. coli W can transport low levels of sucrose that are sufficient to facilitate induction of the csc sucrose catabolism operonSystems analysis of methylerythritol-phosphate pathway flux in E. coli: insights into the role of oxidative stress and the validity of lycopene as an isoprenoid reporter metabolite.Knock-in/Knock-out (KIKO) vectors for rapid integration of large DNA sequences, including whole metabolic pathways, onto the Escherichia coli chromosome at well-characterised loci.Emissions of putative isoprene oxidation products from mango branches under abiotic stress.A unified mechanism of action for volatile isoprenoids in plant abiotic stress.Examining the feasibility of bulk commodity production in Escherichia coli.Metabolic engineering of volatile isoprenoids in plants and microbes.Isoprene.Recent advances in synthetic biology for engineering isoprenoid production in yeast.Isoprene emission protects photosynthesis but reduces plant productivity during drought in transgenic tobacco (Nicotiana tabacum) plants.Isoprene production in transgenic tobacco alters isoprenoid, non-structural carbohydrate and phenylpropanoid metabolism, and protects photosynthesis from drought stress.Dynamic regulation of gene expression using sucrose responsive promoters and RNA interference in Saccharomyces cerevisiae.Controlling heterologous gene expression in yeast cell factories on different carbon substrates and across the diauxic shift: a comparison of yeast promoter activities.Isoprene emissions influence herbivore feeding decisions.Bespoke design of whole-cell microbial machines.Coupling gene regulatory patterns to bioprocess conditions to optimize synthetic metabolic modules for improved sesquiterpene production in yeastDeletion of cscR in Escherichia coli W improves growth and poly-3-hydroxybutyrate (PHB) production from sucrose in fed batch culture.Development of sucrose-utilizing Escherichia coli K-12 strain by cloning β-fructofuranosidases and its application for L-threonine production.Cell-free pipeline for discovery of thermotolerant xylanases and endo-1,4-β-glucanases.The role of isoprene in insect herbivory.Effects of fosmidomycin on plant photosynthesis as measured by gas exchange and chlorophyll fluorescence.Engineered quorum sensing using pheromone-mediated cell-to-cell communication in Saccharomyces cerevisiae.An expanded heterologous <i>GAL</i> promoter collection for diauxie-inducible expression in Saccharomyces cerevisiae.Towards industrial production of isoprenoids in Escherichia coli: lessons learned from CRISPR-Cas9 based optimization of a chromosomally integrated mevalonate pathway.A novel cis-acting element, ESP, contributes to high-level endosperm-specific expression in an oat globulin promoter.The minimal genome comes of age.The Saccharomyces cerevisiae pheromone-response is a metabolically active stationary phase for bio-production.Molecular Cloning Designer Simulator (MCDS): All-in-one molecular cloning and genetic engineering design, simulation and management software for complex synthetic biology and metabolic engineering projects.pGFPGUSPlus, a new binary vector for gene expression studies and optimising transformation systems in plants.A squalene synthase protein degradation method for improved sesquiterpene production in Saccharomyces cerevisiae.HR index--a simple method for the prediction of oxygen uptake.Quorum-sensing linked RNA interference for dynamic metabolic pathway control in Saccharomyces cerevisiae.A transferable sucrose utilization approach for non-sucrose-utilizing Escherichia coli strains.Engineered protein degradation of farnesyl pyrophosphate synthase is an effective regulatory mechanism to increase monoterpene production in Saccharomyces cerevisiae
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Claudia E Vickers
@en
Claudia E Vickers
@es
Claudia E Vickers
@nl
Claudia E Vickers
@sl
Claudia Vickers
@fr
type
label
Claudia E Vickers
@en
Claudia E Vickers
@es
Claudia E Vickers
@nl
Claudia E Vickers
@sl
Claudia Vickers
@fr
prefLabel
Claudia E Vickers
@en
Claudia E Vickers
@es
Claudia E Vickers
@nl
Claudia E Vickers
@sl
Claudia Vickers
@fr
P1053
A-1288-2009
P106
P21
P31
P3829
P496
0000-0002-0792-050X