Literature DB >> 2925629

Nitric oxide and nitrous oxide production and cycling during dissimilatory nitrite reduction by Pseudomonas perfectomarina.

O C Zafiriou1, Q S Hanley, G Snyder.   

Abstract

The denitrifier Pseudomonas perfectomarina reduced nitrite under conditions of kinetic competition between cells and gas sparging for extracellular dissolved nitric and nitrous oxides, NOaq and N2Oaq, in a chemically defined marine medium. Time courses of nitrite reduction and NOg and N2Og alpha removal were integrated to give NOg and N2Og yields. At high sparging rates, the NOg yield was greater than 50% of nitrite-N reduced, and the yield of NOg + N2Og was approximately 75%. Hence interrupted denitrification yields NOaq and N2Oaq as major products. The yields varied with sparging rates in agreement with a quantitative model of denitrification (Betlach, M. P., and Tiedje, J.M. (1981) Appl. Environ. Microbiol. 42, 1074-1084) that applies simplified Michaelis-Menten kinetics to NO2-----NOaq----N2Oaq----N2. The fit gave an estimate of the maximum scavengeable NOaq yield of 73 +/- 8% of nitrite-N. Thus a minor path independent of NOaq is also required. The fit of the model to data at lower sparging rates, where normal denitrification products predominate, implies that the extracellular NOaq pool yield is independent of gas sparging rate. Thus in P. perfectomarina NOaq and N2Oaq are intermediates, or facilely equilibrate with true intermediates, during complete denitrification. The recovery of most nitrite-N as NO and/or N2O under perturbed conditions is not an artifact of irreversible product removal, but an attribute of denitrification in this species, and most probably it is characteristic of denitrification in other species as well.

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Year:  1989        PMID: 2925629

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  11 in total

1.  Nitric oxide signaling and transcriptional control of denitrification genes in Pseudomonas stutzeri.

Authors:  K U Vollack; W G Zumft
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

Review 2.  From no-confidence to nitric oxide acknowledgement: a story of bacterial nitric-oxide reductase.

Authors:  M Koutný
Journal:  Folia Microbiol (Praha)       Date:  2000       Impact factor: 2.099

Review 3.  The biological role of nitric oxide in bacteria.

Authors:  W G Zumft
Journal:  Arch Microbiol       Date:  1993       Impact factor: 2.552

Review 4.  Denitrification: production and consumption of nitric oxide.

Authors:  R W Ye; B A Averill; J M Tiedje
Journal:  Appl Environ Microbiol       Date:  1994-04       Impact factor: 4.792

5.  Mutants of Pseudomonas fluorescens deficient in dissimilatory nitrite reduction are also altered in nitric oxide reduction.

Authors:  R W Ye; A Arunakumari; B A Averill; J M Tiedje
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

Review 6.  Cell biology and molecular basis of denitrification.

Authors:  W G Zumft
Journal:  Microbiol Mol Biol Rev       Date:  1997-12       Impact factor: 11.056

Review 7.  Soil microorganisms as controllers of atmospheric trace gases (H2, CO, CH4, OCS, N2O, and NO).

Authors:  R Conrad
Journal:  Microbiol Rev       Date:  1996-12

8.  Nitric and nitrous oxide reductases are active under aerobic conditions in cells of Thiosphaera pantotropha.

Authors:  L C Bell; S J Ferguson
Journal:  Biochem J       Date:  1991-01-15       Impact factor: 3.857

9.  Assessing the impact of denitrifier-produced nitric oxide on other bacteria.

Authors:  Peter S Choi; Zeki Naal; Charles Moore; Emerilis Casado-Rivera; Hector D Abruña; John D Helmann; James P Shapleigh
Journal:  Appl Environ Microbiol       Date:  2006-03       Impact factor: 4.792

10.  A comparison of NO and N2O production by the autotrophic nitrifier Nitrosomonas europaea and the heterotrophic nitrifier Alcaligenes faecalis.

Authors:  I C Anderson; M Poth; J Homstead; D Burdige
Journal:  Appl Environ Microbiol       Date:  1993-11       Impact factor: 4.792

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