Kinetic and inhibition studies for the aerobic cometabolism of 1,1,1-trichloroethane, 1,1-dichloroethylene, and 1,1-dichloroethane by a butane-grown mixed culture

2002 ◽  
Vol 80 (5) ◽  
pp. 498-508 ◽  
Author(s):  
Young Kim ◽  
Daniel J. Arp ◽  
Lewis Semprini
2005 ◽  
Vol 52 (8) ◽  
pp. 125-131 ◽  
Author(s):  
Y. Kim ◽  
L. Semprini

Aerobic cometabolism of cis-1,2-dichloroethylene (c-DCE) by a butane-grown mixed culture was evaluated in batch kinetic tests. The transformation of c-DCE resulted in the coincident generation of c-DCE epoxide. Chloride release studies showed ∼75% oxidative dechlorination of c-DCE. Mass spectrometry confirmed the presence of a compound with mass-to-charge-fragment ratios of 112, 83, 48, and 35. These values are in agreement with the spectra of chemically synthesized c-DCE epoxide. The transformation of c-DCE required O2, was inhibited by butane and was inactivated by acetylene (a known monooxygenase inactivator), indicating that a butane monooxygenase enzyme was likely involved in the transformation of c-DCE. This study showed c-DCE epoxide was biologically transformed, likely by a butane monooxygenase enzyme. c-DCE epoxide transformation was inhibited by both acetylene and c-DCE indicating a monooxygenase enzyme was involved. The epoxide transformation was also stopped when mercuric chloride (HgCl2) was added as a biological inhibitor, further support a biological transformation. To our knowledge this is the first report of the biological transform c-DCE epoxide by a butane-grown culture.


1998 ◽  
Vol 79 (06) ◽  
pp. 1184-1190 ◽  
Author(s):  
Yoshiaki Tomiyama ◽  
Shigenori Honda ◽  
Kayoko Senzaki ◽  
Akito Tanaka ◽  
Mitsuru Okubo ◽  
...  

SummaryThis study investigated the difference of [Ca2+]i movement in platelets in response to thrombin and TRAP. The involvement of αIIbβ3 in this signaling was also studied. Stimulation of platelets with thrombin at 0.03 U/ml caused platelet aggregation and a two-peak increase in [Ca2+]i. The second peak of [Ca2+]i, but not the first peak was abolished by the inhibition of platelet aggregation with αIIbβ3 antagonists or by scavenging endogenous ADP with apyrase. A cyclooxygenase inhibitor, aspirin, and a TXA2 receptor antagonist, BM13505, also abolished the second peak of [Ca2+]i but not the first peak, although these regents did not inhibit aggregation. Under the same assay conditions, measurement of TXB2 demonstrated that αIIbβ3 antagonists and aspirin almost completely inhibited the production of TXB2. In contrast to thrombin-stimulation, TRAP caused only a single peak of [Ca2+]i even in the presence of platelet aggregation, and a high level of [Ca2+]i increase was needed for the induction of platelet aggregation. The inhibition of aggregation with αIIbβ3 antagonists had no effect on [Ca2+]i change and TXB2 production induced by TRAP. Inhibition studies using anti-GPIb antibodies suggested that GPIb may be involved in the thrombin response, but not in the TRAP. Our findings suggest that low dose thrombin causes a different [Ca2+]i response and TXA2 producing signal from TRAP. Endogenous ADP release and fibrinogen binding to αIIbβ3 are responsible for the synthesis of TXA2 which results in the induction of the second peak of [Ca2+]i in low thrombin- but not TRAP-stimulated platelets.


1974 ◽  
Vol 31 (01) ◽  
pp. 072-085 ◽  
Author(s):  
M Kopitar ◽  
M Stegnar ◽  
B Accetto ◽  
D Lebez

SummaryPlasminogen activator was isolated from disrupted pig leucocytes by the aid of DEAE chromatography, gel filtration on Sephadex G-100 and final purification on CM cellulose, or by preparative gel electrophoresis.Isolated plasminogen activator corresponds No. 3 band of the starting sample of leucocyte cells (that is composed from 10 gel electrophoretic bands).pH optimum was found to be in pH range 8.0–8.5 and the highest pH stability is between pH range 5.0–8.0.Inhibition studies of isolated plasminogen activator were performed with EACA, AMCHA, PAMBA and Trasylol, using Anson and Astrup method. By Astrup method 100% inhibition was found with EACA and Trasylol and 30% with AMCHA. PAMBA gave 60% inhibition already at concentration 10–3 M/ml. Molecular weight of plasminogen activator was determined by gel filtration on Sephadex G-100. The value obtained from 4 different samples was found to be 28000–30500.


Rumen ciliates still have mysterious secrets and influences in ruminants. This study investigated the effect of transfaunation of pure and mixed cultures of rumen ciliates on physical clinical examination, selected serum parameters and milk profile in defaunated lactating dairy goats. A number of 8 Baladi native breed goats were randomly classified into two groups each one containing 4 goats. Pure culture group was transfaunated with 6 ml of pure culture of Holotricha spp., while mixed culture group was transfaunated with 6 ml of mixed culture of 81.85% Holotricha and 18.15% Ophryoscolex spp. once weekly for three consecutive weeks, after defaunation of both groups using 30 ml of 8% SLS for two consecutive days. Serum and milk samples were collected weekly for three successive weeks to study effect of type of ciliate culture, duration of transfaunation and their interaction. Results revealed that transfaunation of pure and mixed cultures of rumen ciliates had no effect on physical examination with minimal non-significant improvement of calcium, inorganic phosphorous, total protein and globulin in serum of defaunated goats. Transfaunation of pure or mixed cultures of rumen ciliates within three weeks could not improve significantly decreased milk fat % of defaunated goats without any effect on other measured milk profile parameters. It is concluded that further investigations on transfaunation without prior defaunation should be performed using different pure and mixed cultures of rumen ciliates for therapeutic and productive purposes.


1995 ◽  
Vol 31 (9) ◽  
pp. 101-107 ◽  
Author(s):  
Chongchin Polprasert ◽  
Charles N. Haas

Anaerobic reactors were operated in a semi-batch mode and fed with the dual substrates glucose (G) plus acetic acid (Ac) as primary organic sources to study the effect of sulfate on COD oxidation. With glucose, COD removal by methane formation was seriously inhibited, resulting in COD accumulation in the reactor. Although acetic acid can be consumed by some sulfate-reducing species, it was not a major substrate for sulfate reduction, but was largely responsible for methane formation in the anaerobic mixed culture used in this study. With dual substrates, extreme inhibition of methanogenesis did not occur as did with glucose alone. Instead, methanogens were found to work in harmony with acid formers as well as sulfate reducers to oxidise COD. Interestingly, from 12-hour monitoring, increased G/Ac COD ratios decreased COD removal rates as well as biogas production, but resulted in higher sulfate reduction. This suggests that there should be an optimal feed G/Ac COD ratio, for which removal of both organics could be maximised.


1995 ◽  
Vol 31 (1) ◽  
pp. 215-225 ◽  
Author(s):  
Gerald E. Speitel ◽  
Robert L. Segar

Aerobic cometabolism of chlorinated aliphatic solvents in biofilm reactors is a potential treatment technology for contaminated water and air streams. This research investigated cometabolism by pure and mixed cultures of methanotrophs and mixed cultures of phenol-degrading bacteria. Initial experiments with continuous-flow, packed-bed bioreactors proved unsuccessful; therefore, the major focus of the work was on sequencing biofilm reactors, which cycle between two modes of operation, degradation of chlorinated solvents and rejuvenation of the microbial population. Particular success was obtained with a mixed culture of phenol degraders in the treatment of chlorinated ethenes (e.g., trichloroethylene - TCE). Under the best operating conditions, 90% removal of TCE occurred at a 14-minute packed-bed hydraulic residence time. The bioreactors required only two, 1.5 h biomass rejuvenation periods per day to sustain this removal. Experiments with Methylosinus trichosporium OB3b were less successful because of the organism's slow growth rate, relatively poor ability to attach to surfaces, and its inability to successfully compete with other methanotrophs in the bioreactor environment. Overall, however, the research demonstrated the potential attractiveness of sequencing biofilm reactors in treating water contaminated with chlorinated solvents.


2014 ◽  
Vol 14 (17) ◽  
pp. 1990-2005 ◽  
Author(s):  
Shalini Saxena ◽  
Janupally Renuka ◽  
Variam Jeankumar ◽  
Perumal Yogeeswari ◽  
Dharmarajan Sriram

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