A metabolic model for thiodiglycol degradation: Capacity constraint leads to byproduct accumulation

Bioprocess and Biosystems Engineering

Volumn 24, Issue 1, 2001, Pages 33-38

  Lee, T S ^a   Chan, S H ^a   Weigand, W ^a   Bentley, W ^a  

^a UNIVERSITY OF MARYLAND   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

[(2 HYDROXYETHYL)THIO]ACETIC ACID; ACETIC ACID; GLYCOL; GLYCOLIC ACID DERIVATIVE; THIODIGLYCOL; UNCLASSIFIED DRUG;

ACHROMOBACTER XYLOSOXIDANS; ANALYTIC METHOD; ARTICLE; BACTERIAL GROWTH; BACTERIUM; CONTROLLED STUDY; DEGRADATION; MATHEMATICAL MODEL; METABOLIC CAPACITY; METABOLISM; MOLECULAR DYNAMICS; MOLECULAR MODEL; NONHUMAN; PARAMETER; PRIORITY JOURNAL; REACTOR;

ACHROMOBACTER XYLOSOXIDANS; ALCALIGENES; BACTERIA (MICROORGANISMS);

EID: 0034779781     PISSN: 16157591     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004490100228     Document Type: Article

References (11)

1. Bioreactor strategies for the treatment of growth-inhibitory waste: An analysis of thiodiglycol degradation, the main hydrolysis product of sulfur mustard
2. Observation of metabolite formation and variable yield in thiodiglycol biodegradation process: Impact on reactor design
3. Biodegradation of thiodiglycol: The major product of sulfur mustard hydrolysis
4. Biocatalytic transformation of [(2-hydroxyethyl)thio]acetic acid and thiodiglycolic acid from thiodiglycol by Alcaligenes xylosoxydans ssp. xylosoxydans (SH91)
5. cis-Halovinylthioacetamido side chain, a new effective structural element for 7β-substitution in cephem and oxacephem antibiotics
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7. 3,4 Diarylthiophenes are selective Cox-2 inhibitors