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Escherichia coli Ethanol

Escherichia coli Ethanol production Integration of pyruvate dearboxylase and alcohol dehydrogenase 11 from Zymomonas mobilis onto the chromosome of E. coli improve d the stability of the genes over the plasmid-based system, and the ethanol yield was near the maximum theoretical yield on 10% glucose and 8% xylose 48, 98... [Pg.197]

In a study directed to the analysis of the role of Fe and the generation of H2O2 in Escherichia coli (McCormick et al. 1998), hydroxyl radicals were specihcally trapped by reaction with ethanol to give the a-hydroxyethyl radical. This formed a stable adduct with a-(4-pyridyl-l-oxide)-iV-t-butyl nitroxide that was not formed either by superoxide or hydroxyl radicals. The role of redox-reactive iron is to use EPR to analyze the EPR-detectable ascorbyl radicals. [Pg.289]

Historically, HCDC was first established for yeasts to produce single-ceU protein, ethanol, and biomass. Later, dense cultures of other mesophiles producing various types of products were developed, e.g.,by Suzuki et al. [96]. The combination of recombinant DNA technology and large-scale culture processes has enabled human proteins to be produced in a number of hosts, in particular in Escherichia coli [97-100]. Approaches to optimize the production of recombinant proteins are the subject of recent reviews from Winter et al. [101]. [Pg.31]

Tincture of the dried seed, on agar plate at a concentration of 30 p,L/disc, was inactive on Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. Extract of 10 g plant material in 100 mL ethanol was used b Anticoagulation activity. Serpin BSZx (an inhibitor of trypsin and chemotrypsin) inhibited thrombin, plasma kallikrein, factor Vlla/tissue factor, and factor Xa at heparin-independent association rates. Only factor Xa turned a significant fraction of BSZx over as substrate. Activated protein C and leukocyte elastase were slowly inhibited by BSZx, whereas factor Xlla, urokinase and tissue type plasminogen activator, plasmin and pancreas kallikrein, and elastase were not or only weakly affected. Trypsin from Fusarium was not inhibited, while interaction with subtilisin Carlsberg and Novo was rapid, but most BSZx was cleaved as a substrate L... [Pg.240]

Antibacterial activity. Decoction of the dried fruit, on agar plate, was inactive on Pseudomonas aeruginosa° K Water extract of the dried fruit, on agar plate, was active on Salmonella typhi, inhibitory concentration (10)5010-3 p.g/mL . Water extract of the dried fruit, on agar plate at a concentration of 62.5 mg/mL, was inactive on Escheri chia coli and Staphylococcus aureus° . Water extract of the dried fruit, on agar plate at a concentration of 1 mg/mL, was inactive on Salmonella typhi . ITot water extract of the dried fruit, on agar plate at a concentration of 62.5 mg/mL, was inactive on Escherichia coli and Staphylococcus aureus° . Ethanol (100%) extract of the fresh leaf, on agar plate, at a concentration of 2.5 mg/disc, was... [Pg.381]

Antimutagenic activity. Ethanol (70%) extract of the dried aerial parts, on agar plate, was inactive on Escherichia coli PQ37 vs mitomycin-induced mutagenesis, assessed by the SOS-chromotest method Antioxidant activity. Hexane and methanol extracts of the dried seed, tested on lard at a concentration of 0.06 %, were inactive Seed oil, at undiluted concentration, was active " . Acetone extract of the seed, at a concentration of 0.2 mg/kg, was active. Linoleic acid was used as a substrate in this test " . [Pg.493]

Yersinia enterolitica °. Ethanol (90%) extract of the dried rhizome, on agar plate at a concentration of 500 mg/disc, produced weak activity on Bacillus subtilis, Escherichia coli. Streptococcus aureus, and Streptococcus faecalis L Hot water extract of the dried rhizome, on agar plate at a concentration of 50 mg/disc, was inactive on Salmonella typhimurium TAIOO and TA98" . [Pg.519]

The metabolism of anaerobic chytrids has not been studied in great detail, but it is known that most anaerobic chytrids studied so far produce formate, acetate, succinate, lactate and ethanol besides hydrogen and carbon dioxide when growing on cellulose, glucose or fructose as a carbon source (Julliand et al. 1998). Such a mixed acid fermentation is very similar to bacterial mixed acid fermentations that are, for example, well known for facultative anaerobic enteric bacteria, such as Escherichia coli. [Pg.151]

Equivalence point e31 Escherichia coli 97, 107 Estradiol 508-509 Ethanol... [Pg.964]


See other pages where Escherichia coli Ethanol is mentioned: [Pg.328]    [Pg.328]    [Pg.419]    [Pg.454]    [Pg.366]    [Pg.59]    [Pg.142]    [Pg.143]    [Pg.154]    [Pg.265]    [Pg.168]    [Pg.766]    [Pg.186]    [Pg.237]    [Pg.44]    [Pg.123]    [Pg.163]    [Pg.177]    [Pg.203]    [Pg.242]    [Pg.249]    [Pg.287]    [Pg.422]    [Pg.492]    [Pg.519]    [Pg.537]    [Pg.900]    [Pg.248]    [Pg.63]   
See also in sourсe #XX -- [ Pg.44 , Pg.56 , Pg.302 ]




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