B A van de Pas, S Jansen, C Dijkema, G Schraa, W M de Vos, A J Stams
Index: Appl. Environ. Microbiol. 67(9) , 3958-63, (2001)
Full Text: HTML
The amount of energy that can be conserved via halorespiration by Desulfitobacterium dehalogenans JW/IU-DC1 was determined by comparison of the growth yields of cells grown with 3-chloro-4-hydroxyphenyl acetate (Cl-OHPA) and different electron donors. Cultures that were grown with lactate, pyruvate, formate, or hydrogen as an electron donor and Cl-OHPA as an electron acceptor yielded 3.1, 6.6, 1.6, and 1.6 g (dry weight) per mol of reduction equivalents, respectively. Fermentative growth on pyruvate yielded 14 g (dry weight) per mol of pyruvate oxidized. Pyruvate was not fermented stoichiometrically to acetate and lactate, but an excess of acetate was produced. Experiments with 13C-labeled bicarbonate showed that during pyruvate fermentation, approximately 9% of the acetate was formed from the reduction of CO2. Comparison of the growth yields suggests that 1 mol of ATP is produced per mol of acetate produced by substrate-level phosphorylation and that there is no contribution of electron transport phosphorylation when D. dehalogenans grows on lactate plus Cl-OHPA or pyruvate plus Cl-OHPA. Furthermore, the growth yields indicate that approximately 1/3 mol of ATP is conserved per mol of Cl-OHPA reduced in cultures grown in formate plus Cl-OHPA and hydrogen plus Cl-OHPA. Because neither formate nor hydrogen nor Cl-OHPA supports substrate-level phosphorylation, energy must be conserved through the establishment of a proton motive force. Pyruvate ferredoxin oxidoreductase, lactate dehydrogenase, formate dehydrogenase, and hydrogenase were localized by in vitro assays with membrane-impermeable electron acceptors and donors. The orientation of chlorophenol-reductive dehalogenase in the cytoplasmic membrane, however, could not be determined. A model is proposed, which may explain the topology analyses as well as the results obtained in the yield study.
Structure | Name/CAS No. | Molecular Formula | Articles |
---|---|---|---|
![]() |
3-Chloro-4-hydroxyphenylacetic acid
CAS:33697-81-3 |
C8H7ClO3 |
CprK crystal structures reveal mechanism for transcriptional...
2006-09-22 [J. Biol. Chem. 281(38) , 28318-25, (2006)] |
Degradation of 4-chlorophenylacetic acid by a Pseudomonas sp...
1981-04-01 [J. Bacteriol. 146(1) , 64-8, (1981)] |
[Microbial degradation and 4-chlorophenylacetic acid. Chemic...
1982-04-01 [Hoppe. Seylers. Z. Physiol. Chem. 363(4) , 431-7, (1982)] |
Auxin influx inhibitors 1-NOA, 2-NOA, and CHPAA interfere wi...
2010-08-01 [J. Exp. Bot. 61(13) , 3589-98, (2010)] |
Novel auxin transport inhibitors phenocopy the auxin influx ...
2001-02-01 [Plant J. 25(4) , 399-406, (2001)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved