Engineering butanol-tolerance in escherichia coli with artificial transcription factor libraries.
about
Bacterial sigma factors as targets for engineered or synthetic transcriptional controlThe future of metabolic engineering and synthetic biology: towards a systematic practiceProduction of Fatty Acid-derived valuable chemicals in synthetic microbesGenome-wide Escherichia coli stress response and improved tolerance towards industrially relevant chemicalsSelf-regulated 1-butanol production in Escherichia coli based on the endogenous fermentative controlSignificant rewiring of the transcriptome and proteome of an Escherichia coli strain harboring a tailored exogenous global regulator IrrE.Enhancing E. coli isobutanol tolerance through engineering its global transcription factor cAMP receptor protein (CRP).Combinatorial and high-throughput screening approaches for strain engineering.Improvement of acetic acid tolerance of Saccharomyces cerevisiae using a zinc-finger-based artificial transcription factor and identification of novel genes involved in acetic acid tolerance.Rapid prototyping of microbial cell factories via genome-scale engineering.Raman spectroscopy detects phenotypic differences among Escherichia coli enriched for 1-butanol tolerance using a metagenomic DNA library.Enhanced cellulase production from Trichoderma reesei Rut-C30 by engineering with an artificial zinc finger protein library.Manipulation of the carbon storage regulator system for metabolite remodeling and biofuel production in Escherichia coliMetabolic flux analysis of heterotrophic growth in Chlamydomonas reinhardtii.Genome replication engineering assisted continuous evolution (GREACE) to improve microbial tolerance for biofuels productionCombinatorial approaches for inverse metabolic engineering applications.Protein engineering for metabolic engineering: current and next-generation tools.Regulatory mechanisms related to biofuel tolerance in producing microbes.Enhancing microbial production of biofuels by expanding microbial metabolic pathways.Extending CRISPR-Cas9 Technology from Genome Editing to Transcriptional Engineering in the Genus Clostridium.Micelle-mediated transport disturbance providing extracellular strategy for alleviating n-butanol stress on Escherichia coli.CAR1 deletion by CRISPR/Cas9 reduces formation of ethyl carbamate from ethanol fermentation by Saccharomyces cerevisiae.Engineering a homobutanol fermentation pathway in Escherichia coli EG03.
P2860
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P2860
Engineering butanol-tolerance in escherichia coli with artificial transcription factor libraries.
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Engineering butanol-tolerance ...... ranscription factor libraries.
@ast
Engineering butanol-tolerance ...... ranscription factor libraries.
@en
type
label
Engineering butanol-tolerance ...... ranscription factor libraries.
@ast
Engineering butanol-tolerance ...... ranscription factor libraries.
@en
prefLabel
Engineering butanol-tolerance ...... ranscription factor libraries.
@ast
Engineering butanol-tolerance ...... ranscription factor libraries.
@en
P2093
P2860
P356
P1476
Engineering butanol-tolerance ...... ranscription factor libraries.
@en
P2093
Bong Hyun Sung
Ju Young Lee
Kyung Seok Yang
Sun Chang Kim
P2860
P304
P356
10.1002/BIT.22989
P577
2010-11-23T00:00:00Z