Angewandte Chemie International Edition, ISSN 1433-7851, 12/2009, Volume 48, Issue 50, pp. 9426 - 9451
The amount of research activity concerning α‐methylene‐γ‐butyrolactones and α‐alkylidene‐γ‐butyrolactones has increased dramatically in recent years. This...
natural products | bioactivity | α‐alkylidene‐γ‐butyrolactones | α‐methylene‐γ‐butyrolactones | biosynthesis | α-alkylidene-γ- butyrolactones | Bioactivity | Biosynthesis | Natural products | α-methylene-γ-butyrolactones | CROSS-METATHESIS | DREIDING-SCHMIDT REACTIONS | CATALYZED STEREOSELECTIVE-SYNTHESIS | HIGHLY OXYGENATED 1,10-SECO-EUDESMANOLIDES | BIOLOGICAL-ACTIVITIES | CYTOTOXIC ACTIVITY | CHEMISTRY, MULTIDISCIPLINARY | SESQUITERPENE LACTONES | a-alkylidene-gamma-butyrolactones | CORAL LOBOPHYTUM-CRASSUM | AERIAL PARTS | alpha-methylene-gamma-butyrolactones | ENANTIOSELECTIVE TOTAL-SYNTHESIS | 4-Butyrolactone - therapeutic use | 4-Butyrolactone - biosynthesis | 4-Butyrolactone - chemical synthesis | Molecular Structure | Structure-Activity Relationship | 4-Butyrolactone - analogs & derivatives | Drug Evaluation, Preclinical
natural products | bioactivity | α‐alkylidene‐γ‐butyrolactones | α‐methylene‐γ‐butyrolactones | biosynthesis | α-alkylidene-γ- butyrolactones | Bioactivity | Biosynthesis | Natural products | α-methylene-γ-butyrolactones | CROSS-METATHESIS | DREIDING-SCHMIDT REACTIONS | CATALYZED STEREOSELECTIVE-SYNTHESIS | HIGHLY OXYGENATED 1,10-SECO-EUDESMANOLIDES | BIOLOGICAL-ACTIVITIES | CYTOTOXIC ACTIVITY | CHEMISTRY, MULTIDISCIPLINARY | SESQUITERPENE LACTONES | a-alkylidene-gamma-butyrolactones | CORAL LOBOPHYTUM-CRASSUM | AERIAL PARTS | alpha-methylene-gamma-butyrolactones | ENANTIOSELECTIVE TOTAL-SYNTHESIS | 4-Butyrolactone - therapeutic use | 4-Butyrolactone - biosynthesis | 4-Butyrolactone - chemical synthesis | Molecular Structure | Structure-Activity Relationship | 4-Butyrolactone - analogs & derivatives | Drug Evaluation, Preclinical
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 03/2013, Volume 51, Issue 5, pp. 1137 - 1146
Aluminum‐based salen and salan complexes mediate the ring‐opening polymerization (ROP) of rac‐β‐butyrolactone (β‐BL), rac‐lactide, and ε‐caprolactone. Al‐salen...
copolymerization | ring‐opening polymerization | rac‐lactide | biodegradable | rac‐β‐butyrolactone | rac-β-butyrolactone | rac-lactide | ring-opening polymerization | rac-ss-butyrolactone | POLYMER SCIENCE | ACID | PREDOMINANTLY SYNDIOTACTIC POLY(BETA-HYDROXYBUTYRATE) | BETA-D,L-BUTYROLACTONE | RACEMIC LACTIDE | STEREOELECTIVE POLYMERIZATION | EPSILON-CAPROLACTONE | LACTONES | BIODEGRADABLE ALIPHATIC POLYESTERS | CHAIN-END CONTROL | METAL-COMPLEXES
copolymerization | ring‐opening polymerization | rac‐lactide | biodegradable | rac‐β‐butyrolactone | rac-β-butyrolactone | rac-lactide | ring-opening polymerization | rac-ss-butyrolactone | POLYMER SCIENCE | ACID | PREDOMINANTLY SYNDIOTACTIC POLY(BETA-HYDROXYBUTYRATE) | BETA-D,L-BUTYROLACTONE | RACEMIC LACTIDE | STEREOELECTIVE POLYMERIZATION | EPSILON-CAPROLACTONE | LACTONES | BIODEGRADABLE ALIPHATIC POLYESTERS | CHAIN-END CONTROL | METAL-COMPLEXES
Journal Article
Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences, ISSN 1364-503X, 08/2017, Volume 375, Issue 2101, p. 20170003
Multivinyl-functionalized gamma-butyrolactones, gamma-vinyl-gamma-methyl-alpha-methylene-gamma-butyrolactone (gamma VMMBL) and...
Lewis pair polymerization | γ-vinyl-γ-methyl-α-methylene-γ-butyrolactone | γ-allyl-γ-methyl-α-methylene-γ-butyrolactone | PROTON-TRANSFER POLYMERIZATION | ORGANOCATALYTIC LIVING POLYMERIZATION | COORDINATION POLYMERIZATION | CONJUGATE-ADDITION | METHYL-METHACRYLATE | MULTIDISCIPLINARY SCIENCES | N-HETEROCYCLIC CARBENES | TRANSFER RADICAL POLYMERIZATION | gamma-allyl-gamma-methyl-alpha-methylene-gamma-butyrolactone | ALLYL METHACRYLATE | gamma-vinyl-gamma-methyl-alpha-methylene-gamma-butyrolactone | VINYL METHACRYLATE | RING-OPENING POLYMERIZATION | 143 | 1002 | 117 | 108 | 142
Lewis pair polymerization | γ-vinyl-γ-methyl-α-methylene-γ-butyrolactone | γ-allyl-γ-methyl-α-methylene-γ-butyrolactone | PROTON-TRANSFER POLYMERIZATION | ORGANOCATALYTIC LIVING POLYMERIZATION | COORDINATION POLYMERIZATION | CONJUGATE-ADDITION | METHYL-METHACRYLATE | MULTIDISCIPLINARY SCIENCES | N-HETEROCYCLIC CARBENES | TRANSFER RADICAL POLYMERIZATION | gamma-allyl-gamma-methyl-alpha-methylene-gamma-butyrolactone | ALLYL METHACRYLATE | gamma-vinyl-gamma-methyl-alpha-methylene-gamma-butyrolactone | VINYL METHACRYLATE | RING-OPENING POLYMERIZATION | 143 | 1002 | 117 | 108 | 142
Journal Article
Polimery/Polymers, ISSN 0032-2725, 2017, Volume 62, Issue 4, pp. 272 - 282
gamma-Butyrolactone (gamma-BL) derivatives are reviewed from the point of view of their ability to form polymers by ring-opening polymerization. The...
Thermodynamic limitations | Ring-opening polymerization | γ-butyrolactone derivatives | Homopolymerization of γ-butyrolactone | γ-butyrolactone | POLYMERS | POLYMER SCIENCE | ACID | gamma-butyrolactone derivatives | MONOMER | thermodynamic limitations | POLYESTER | homopolymerization of gamma-butyrolactone | ring-opening polymerization | LACTONES | gamma-butyrolactone | INHIBITORS | COPOLYMERIZATION
Thermodynamic limitations | Ring-opening polymerization | γ-butyrolactone derivatives | Homopolymerization of γ-butyrolactone | γ-butyrolactone | POLYMERS | POLYMER SCIENCE | ACID | gamma-butyrolactone derivatives | MONOMER | thermodynamic limitations | POLYESTER | homopolymerization of gamma-butyrolactone | ring-opening polymerization | LACTONES | gamma-butyrolactone | INHIBITORS | COPOLYMERIZATION
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 10/2018, Volume 56, Issue 20, pp. 2271 - 2279
ABSTRACT This work investigates effects of poly(γ‐butyrolactone) (PγBL) with different initiation and termination chain ends on five types of materials...
thermal stability | hydrolytic degradation | poly(γ‐butyrolactone) | post‐functionalization | post-functionalization | poly(γ-butyrolactone) | POLYMER SCIENCE | PROTECTION | COPOLYESTERS | poly(-butyrolactone) | ALIPHATIC POLYESTER | LIGANDS | CHEMISTRY | LACTIDE | RECENT PROGRESS | RING-OPENING POLYMERIZATION | CYCLIC POLYMERS | METAL-COMPLEXES | Mechanical properties | Polymers | Lactones | Degradation | Capping | Chain dynamics | Recyclability | Butyrolactone | Dynamic stability | Thermodynamic properties | Chemical synthesis | Thermal stability | Material properties
thermal stability | hydrolytic degradation | poly(γ‐butyrolactone) | post‐functionalization | post-functionalization | poly(γ-butyrolactone) | POLYMER SCIENCE | PROTECTION | COPOLYESTERS | poly(-butyrolactone) | ALIPHATIC POLYESTER | LIGANDS | CHEMISTRY | LACTIDE | RECENT PROGRESS | RING-OPENING POLYMERIZATION | CYCLIC POLYMERS | METAL-COMPLEXES | Mechanical properties | Polymers | Lactones | Degradation | Capping | Chain dynamics | Recyclability | Butyrolactone | Dynamic stability | Thermodynamic properties | Chemical synthesis | Thermal stability | Material properties
Journal Article
Applied Microbiology and Biotechnology, ISSN 0175-7598, 12/2014, Volume 98, Issue 23, pp. 9713 - 9721
The Streptomyces antibiotic regulatory protein (SARP) family regulators have been shown to control the production of secondary metabolites in many Streptomyces...
Life Sciences | Biotechnology | γ-Butyrolactone autoregulator | Microbiology | Microbial Genetics and Genomics | Streptomyces | Secondary metabolism | Indigoidine | CONJUGAL TRANSFER | VIRGINIAMYCIN PRODUCTION | ESCHERICHIA-COLI | BUTYROLACTONE AUTOREGULATOR | ANTIBIOTIC PRODUCTION | TRANSCRIPTIONAL REGULATOR | gamma-Butyrolactone autoregulator | BLUE PIGMENT PRODUCTION | GAMMA-BUTYROLACTONE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | COELICOLOR A3 | Streptomyces - genetics | Repressor Proteins - genetics | Gene Expression Profiling | Transcription Factors - genetics | Pigments, Biological - metabolism | Streptomyces - metabolism | Transcription Factors - metabolism | Biosynthetic Pathways - genetics | Genes, Regulator | Transcription, Genetic | Piperidones - metabolism | Gene Expression Regulation, Bacterial | Repressor Proteins - metabolism | Antibiotics | Bacterial proteins | Physiological aspects | Genetic aspects | Research | Gene expression | Studies | Metabolites | Analysis | Bacteria | Antimicrobial agents | Biosynthesis | Metabolism
Life Sciences | Biotechnology | γ-Butyrolactone autoregulator | Microbiology | Microbial Genetics and Genomics | Streptomyces | Secondary metabolism | Indigoidine | CONJUGAL TRANSFER | VIRGINIAMYCIN PRODUCTION | ESCHERICHIA-COLI | BUTYROLACTONE AUTOREGULATOR | ANTIBIOTIC PRODUCTION | TRANSCRIPTIONAL REGULATOR | gamma-Butyrolactone autoregulator | BLUE PIGMENT PRODUCTION | GAMMA-BUTYROLACTONE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | COELICOLOR A3 | Streptomyces - genetics | Repressor Proteins - genetics | Gene Expression Profiling | Transcription Factors - genetics | Pigments, Biological - metabolism | Streptomyces - metabolism | Transcription Factors - metabolism | Biosynthetic Pathways - genetics | Genes, Regulator | Transcription, Genetic | Piperidones - metabolism | Gene Expression Regulation, Bacterial | Repressor Proteins - metabolism | Antibiotics | Bacterial proteins | Physiological aspects | Genetic aspects | Research | Gene expression | Studies | Metabolites | Analysis | Bacteria | Antimicrobial agents | Biosynthesis | Metabolism
Journal Article
Current Drug Metabolism, ISSN 1389-2002, 2018, Volume 19, Issue 13, pp. 1080 - 1085
Background: Recently, Gamma-hydroxybutyrate (GHB) consumption in the recreational setting has been replaced by that of its prodrug Gamma-butyrolactone (GBL),...
γ-hydroxybutyrate (GHB) | γ-butyrolactone (GBL) | Abuse | Chemsex | Liquid G | Dependence | liquid G | gamma-hydroxybutyrate (GHB) | abuse | BIOCHEMISTRY & MOLECULAR BIOLOGY | BUTYROLACTONE GBL | 1,4-BUTANEDIOL | gamma-butyrolactone (GBL) | INTOXICATION | GABA(B) | dependence | PHARMACOLOGY & PHARMACY | chemsex | WITHDRAWAL | PRECURSORS | GAMMA-HYDROXYBUTYRATE GHB | Drug abuse | Toxicity | Oral administration | Central nervous system | Health risks | Mass spectroscopy | Pharmacology | Industrial applications | Liquid chromatography | Bioavailability | High-performance liquid chromatography | Toxicology | Liability | Laws | Rodents | Butyrolactone | g-Hydroxybutyric acid | Mass spectrometry | Public health | Lipophilicity | High performance liquid chromatography | Acute toxicity
γ-hydroxybutyrate (GHB) | γ-butyrolactone (GBL) | Abuse | Chemsex | Liquid G | Dependence | liquid G | gamma-hydroxybutyrate (GHB) | abuse | BIOCHEMISTRY & MOLECULAR BIOLOGY | BUTYROLACTONE GBL | 1,4-BUTANEDIOL | gamma-butyrolactone (GBL) | INTOXICATION | GABA(B) | dependence | PHARMACOLOGY & PHARMACY | chemsex | WITHDRAWAL | PRECURSORS | GAMMA-HYDROXYBUTYRATE GHB | Drug abuse | Toxicity | Oral administration | Central nervous system | Health risks | Mass spectroscopy | Pharmacology | Industrial applications | Liquid chromatography | Bioavailability | High-performance liquid chromatography | Toxicology | Liability | Laws | Rodents | Butyrolactone | g-Hydroxybutyric acid | Mass spectrometry | Public health | Lipophilicity | High performance liquid chromatography | Acute toxicity
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 03/2013, Volume 51, Issue 5, pp. 1185 - 1196
A series of zinc benzylalkoxide complexes, [LnZn(μ‐OBn)]2 (L = L1H–L5H), supported by NNO‐tridentate ketiminate ligands with various electron...
ε‐decalactone | L‐lactide | β‐butyrolactone | polyethers | catalysts | ε‐caprolactone | ring‐opening polymerization (ROP) | zinc | ε-decalactone | ε-caprolactone | ring-opening polymerization (ROP) | β-butyrolactone | L -lactide | POLYMER SCIENCE | STEREOSELECTIVE POLYMERIZATION | ALUMINUM COMPLEXES | e-caprolactone | STRUCTURAL-CHARACTERIZATION | RAC-LACTIDE | e-decalactone | ss-butyrolactone | RACEMIC LACTIDE | EPSILON-CAPROLACTONE | L-lactide | RING-OPENING POLYMERIZATION | SCHIFF-BASE LIGANDS | METAL-COMPLEXES | Polymerization | Polyols | Ligands | Zinc
ε‐decalactone | L‐lactide | β‐butyrolactone | polyethers | catalysts | ε‐caprolactone | ring‐opening polymerization (ROP) | zinc | ε-decalactone | ε-caprolactone | ring-opening polymerization (ROP) | β-butyrolactone | L -lactide | POLYMER SCIENCE | STEREOSELECTIVE POLYMERIZATION | ALUMINUM COMPLEXES | e-caprolactone | STRUCTURAL-CHARACTERIZATION | RAC-LACTIDE | e-decalactone | ss-butyrolactone | RACEMIC LACTIDE | EPSILON-CAPROLACTONE | L-lactide | RING-OPENING POLYMERIZATION | SCHIFF-BASE LIGANDS | METAL-COMPLEXES | Polymerization | Polyols | Ligands | Zinc
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 09/2017, Volume 27, Issue 17, pp. 4199 - 4203
The new lignano-9,9′-lactones (α,β-dibenzyl-γ-butyrolactone lignans), which showed the higher cytotoxicity than arctigenin, were synthesized. The well-known...
Arctigenin | Lignano-9,9′-lactone | Lignan | α,β-Dibenzyl-γ-butyrolactone | γ-Butyrolactone | Matairesinol | Lignano-9,9 '-lactone | CELLS | APOPTOSIS | LIGNAN LACTONES | CHEMISTRY, MEDICINAL | ASYMMETRIC-SYNTHESIS | NATURAL-PRODUCTS | CHEMISTRY, ORGANIC | (-)-MATAIRESINOL | INDUCTION | (-)-ARCTIGENIN | REARRANGEMENT | alpha,beta-Dibenzyl-gamma-butyrolactone | gamma-Butyrolactone | Hydrocarbons, Aromatic - pharmacology | Lignans - chemistry | Antineoplastic Agents - chemical synthesis | Furans - pharmacology | Humans | Molecular Conformation | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Lignans - pharmacology | Dose-Response Relationship, Drug | Hydrocarbons, Aromatic - chemistry | Halogens - pharmacology | Furans - chemistry | HL-60 Cells | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Halogens - chemistry | Lignans - chemical synthesis | Furans - chemical synthesis | HeLa Cells | Drug Screening Assays, Antitumor | Epoxy resins | Resveratrol
Arctigenin | Lignano-9,9′-lactone | Lignan | α,β-Dibenzyl-γ-butyrolactone | γ-Butyrolactone | Matairesinol | Lignano-9,9 '-lactone | CELLS | APOPTOSIS | LIGNAN LACTONES | CHEMISTRY, MEDICINAL | ASYMMETRIC-SYNTHESIS | NATURAL-PRODUCTS | CHEMISTRY, ORGANIC | (-)-MATAIRESINOL | INDUCTION | (-)-ARCTIGENIN | REARRANGEMENT | alpha,beta-Dibenzyl-gamma-butyrolactone | gamma-Butyrolactone | Hydrocarbons, Aromatic - pharmacology | Lignans - chemistry | Antineoplastic Agents - chemical synthesis | Furans - pharmacology | Humans | Molecular Conformation | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Lignans - pharmacology | Dose-Response Relationship, Drug | Hydrocarbons, Aromatic - chemistry | Halogens - pharmacology | Furans - chemistry | HL-60 Cells | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Halogens - chemistry | Lignans - chemical synthesis | Furans - chemical synthesis | HeLa Cells | Drug Screening Assays, Antitumor | Epoxy resins | Resveratrol
Journal Article
Macromolecules, ISSN 0024-9297, 06/2016, Volume 49, Issue 11, pp. 4047 - 4056
A new class of superabsorbent hydrogels was synthesized by copolymerization of acrylamide with sodium 4-hydroxy-2-methylenebutanoate (SHMB). SHMB is obtained...
PROPAGATION RATE COEFFICIENTS | RESOURCES | IONIZED ACRYLIC-ACID | POLYMER SCIENCE | METHYLENE-GAMMA-BUTYROLACTONE | POLY(ALPHA-METHYLENE-GAMMA-BUTYROLACTONE) | KINETICS | POLYMERIZATION | RADICAL COPOLYMERIZATION | METHACRYLATE | AQUEOUS-SOLUTION
PROPAGATION RATE COEFFICIENTS | RESOURCES | IONIZED ACRYLIC-ACID | POLYMER SCIENCE | METHYLENE-GAMMA-BUTYROLACTONE | POLY(ALPHA-METHYLENE-GAMMA-BUTYROLACTONE) | KINETICS | POLYMERIZATION | RADICAL COPOLYMERIZATION | METHACRYLATE | AQUEOUS-SOLUTION
Journal Article
Journal of Industrial Microbiology & Biotechnology, ISSN 1367-5435, 10/2014, Volume 41, Issue 10, pp. 1517 - 1524
There has been a significant global interest to produce bulk chemicals from renewable resources using engineered microorganisms. Large research programs have...
Biochemistry, general | Homoserine | Biotechnology | 1,4-Butanediol | Microbiology | γ-Butyrolactone derivatives | Homoserine lactone | Bio C4 chemicals | Life Sciences | Genetic Engineering | γ-Butyrolactone | Succinic acid | Inorganic Chemistry | Industrial biotechnology | Bioinformatics | O -Succinyl- l -homoserine | O-Succinyl- l-homoserine | O-Succinyl-l-homoserine | O-Succinyl-L-homoserine | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ESCHERICHIA-COLI | GENES | gamma-Butyrolactone | gamma-Butyrolactone derivatives | Hydrolysis | Bioreactors | Escherichia coli - genetics | Succinic Acid - metabolism | 4-Butyrolactone - biosynthesis | Escherichia coli - metabolism | Homoserine - biosynthesis | Solubility | 4-Butyrolactone - analogs & derivatives | Homoserine - analogs & derivatives | Fermentation | Butylene Glycols - metabolism
Biochemistry, general | Homoserine | Biotechnology | 1,4-Butanediol | Microbiology | γ-Butyrolactone derivatives | Homoserine lactone | Bio C4 chemicals | Life Sciences | Genetic Engineering | γ-Butyrolactone | Succinic acid | Inorganic Chemistry | Industrial biotechnology | Bioinformatics | O -Succinyl- l -homoserine | O-Succinyl- l-homoserine | O-Succinyl-l-homoserine | O-Succinyl-L-homoserine | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ESCHERICHIA-COLI | GENES | gamma-Butyrolactone | gamma-Butyrolactone derivatives | Hydrolysis | Bioreactors | Escherichia coli - genetics | Succinic Acid - metabolism | 4-Butyrolactone - biosynthesis | Escherichia coli - metabolism | Homoserine - biosynthesis | Solubility | 4-Butyrolactone - analogs & derivatives | Homoserine - analogs & derivatives | Fermentation | Butylene Glycols - metabolism
Journal Article
Polymer Chemistry, ISSN 1759-9954, 2017, Volume 8, Issue 47, pp. 7369 - 7374
Poly(ε-caprolactones) (PCLs) with low catalyst loading and high molecular weights are highly desired considering their practical applications. In this work,...
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 09/2011, Volume 49, Issue 18, pp. 4027 - 4036
A series of efficient zinc catalysts supported by sterically bulky benzotriazole phenoxide (BTP) ligands are synthesized and structurally characterized. The...
benzotriazole phenoxide | β‐butyrolactone | ring‐opening polymerization | biodegradable | catalysts | living polymerization | ε‐caprolactone | zinc | polyesters | ε-caprolactone | β-butyrolactone | ring-opening polymerization | POLYMER SCIENCE | ALUMINUM COMPLEXES | ALKOXIDES | MAGNESIUM | LACTONES | epsilon-caprolactone | IMMORTAL POLYMERIZATION | LACTIDE | beta-butyrolactone | INITIATORS
benzotriazole phenoxide | β‐butyrolactone | ring‐opening polymerization | biodegradable | catalysts | living polymerization | ε‐caprolactone | zinc | polyesters | ε-caprolactone | β-butyrolactone | ring-opening polymerization | POLYMER SCIENCE | ALUMINUM COMPLEXES | ALKOXIDES | MAGNESIUM | LACTONES | epsilon-caprolactone | IMMORTAL POLYMERIZATION | LACTIDE | beta-butyrolactone | INITIATORS
Journal Article
Journal of Heterocyclic Chemistry, ISSN 0022-152X, 08/2018, Volume 55, Issue 8, pp. 1986 - 1990
An efficient and versatile linear synthesis of γ‐butyrolactone subunit of polycavernolide A has been reported in 14.2% overall yield with 10 linear steps by...
Journal Article
Metabolic Engineering, ISSN 1096-7176, 05/2017, Volume 41, pp. 39 - 45
3-Hydroxy-γ-butyrolactone (3HBL) is an attractive building block owing to its broad applications in pharmaceutical industry. Currently, 3HBL is commercially...
Metabolic engineering | 3-hydroxy-γ-butyrolactone | Escherichia coli | Xylose metabolism | 4-dihydroxybutyric acid | 3-hydroxy-gamma-butyrolactone | K-12 | ALDEHYDE | CHEMICALS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | (S)-3-HYDROXY-GAMMA-BUTYROLACTONE | ENGINEERING NONPHOSPHORYLATIVE METABOLISM | DEHYDROGENASE | 4-Butyrolactone - genetics | 4-Butyrolactone - metabolism | Metabolic Engineering - methods | Xylose - metabolism | Escherichia coli - genetics | Escherichia coli - metabolism | 4-Butyrolactone - analogs & derivatives | Hydroxybutyrates - metabolism | Xylose - genetics | Glucose | Dextrose | Resveratrol | Yuan (China) | Lactones
Metabolic engineering | 3-hydroxy-γ-butyrolactone | Escherichia coli | Xylose metabolism | 4-dihydroxybutyric acid | 3-hydroxy-gamma-butyrolactone | K-12 | ALDEHYDE | CHEMICALS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | (S)-3-HYDROXY-GAMMA-BUTYROLACTONE | ENGINEERING NONPHOSPHORYLATIVE METABOLISM | DEHYDROGENASE | 4-Butyrolactone - genetics | 4-Butyrolactone - metabolism | Metabolic Engineering - methods | Xylose - metabolism | Escherichia coli - genetics | Escherichia coli - metabolism | 4-Butyrolactone - analogs & derivatives | Hydroxybutyrates - metabolism | Xylose - genetics | Glucose | Dextrose | Resveratrol | Yuan (China) | Lactones
Journal Article