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      The metabolic impact of extracellular nitrite on aerobic metabolism of Paracoccus denitrificans

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          Abstract

          Nitrite, in equilibrium with free nitrous acid (FNA), can inhibit both aerobic and anaerobic growth of microbial communities through bactericidal activities that have considerable potential for control of microbial growth in a range of water systems. There has been much focus on the effect of nitrite/FNA on anaerobic metabolism and so, to enhance understanding of the metabolic impact of nitrite/FNA on aerobic metabolism, a study was undertaken with a model denitrifying bacterium Paracoccus denitrificans PD1222. Extracellular nitrite inhibits aerobic growth of P. denitrificans in a pH-dependent manner that is likely to be a result of both nitrite and free nitrous acid (p K a  = 3.25) and subsequent reactive nitrogen oxides generated from the intracellular passage of FNA into P. denitrificans. Increased expression of a gene encoding a flavohemoglobin protein (Fhp) (Pden_1689) was observed in response to extracellular nitrite. Construction and analysis of a deletion mutant established Fhp to be involved in endowing nitrite/FNA resistance at high extracellular nitrite concentrations. Global transcriptional analysis confirmed nitrite-dependent expression of fhp and indicated that P. denitrificans expressed a number of stress response systems associated with protein, DNA and lipid repair. It is therefore suggested that nitrite causes a pH-dependent stress response that is due to the production of associated reactive nitrogen species, such as nitric oxide from the internalisation of FNA.

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          Highlights

          • Paracoccus denitrificans was studied to assess the impact of nitrite on aerobic metabolism.

          • Extracellular nitrite inhibits aerobic growth of P. denitrificans in a pH-dependent manner.

          • Increased expression of a flavohemoglobin was observed in response to extracellular nitrite.

          • Analysis of a mutant established flavohemoglobin to be involved in nitrite tolerance.

          • Only ∼ 1.5% of the genome was differentially regulated in response to nitrite ‘stress’.

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          Most cited references24

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          Involvement of nitric oxide in biofilm dispersal of Pseudomonas aeruginosa.

          Bacterial biofilms at times undergo regulated and coordinated dispersal events where sessile biofilm cells convert to free-swimming, planktonic bacteria. In the opportunistic pathogen Pseudomonas aeruginosa, we previously observed that dispersal occurs concurrently with three interrelated processes within mature biofilms: (i) production of oxidative or nitrosative stress-inducing molecules inside biofilm structures, (ii) bacteriophage induction, and (iii) cell lysis. Here we examine whether specific reactive oxygen or nitrogen intermediates play a role in cell dispersal from P. aeruginosa biofilms. We demonstrate the involvement of anaerobic respiration processes in P. aeruginosa biofilm dispersal and show that nitric oxide (NO), used widely as a signaling molecule in biological systems, causes dispersal of P. aeruginosa biofilm bacteria. Dispersal was induced with low, sublethal concentrations (25 to 500 nM) of the NO donor sodium nitroprusside (SNP). Moreover, a P. aeruginosa mutant lacking the only enzyme capable of generating metabolic NO through anaerobic respiration (nitrite reductase, DeltanirS) did not disperse, whereas a NO reductase mutant (DeltanorCB) exhibited greatly enhanced dispersal. Strategies to induce biofilm dispersal are of interest due to their potential to prevent biofilms and biofilm-related infections. We observed that exposure to SNP (500 nM) greatly enhanced the efficacy of antimicrobial compounds (tobramycin, hydrogen peroxide, and sodium dodecyl sulfate) in the removal of established P. aeruginosa biofilms from a glass surface. Combined exposure to both NO and antimicrobial agents may therefore offer a novel strategy to control preestablished, persistent P. aeruginosa biofilms and biofilm-related infections.
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            Inhibition of nitrification by ammonia and nitrous acid.

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              Bacterial respiration: a flexible process for a changing environment.

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                Author and article information

                Contributors
                Journal
                Water Res
                Water Res
                Water Research
                Pergamon Press
                0043-1354
                1879-2448
                15 April 2017
                15 April 2017
                : 113
                : 207-214
                Affiliations
                [a ]School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK
                [b ]Advanced Water Management Centre (AWMC), University of Queensland, St Lucia, Brisbane, QLD, 4072, Australia
                Author notes
                []Corresponding author. d.richardson@ 123456uea.ac.uk
                Article
                S0043-1354(17)30086-6
                10.1016/j.watres.2017.02.011
                5339346
                28214776
                bfe78ee1-c384-4434-83d9-4f55f090c78f
                © 2017 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 26 October 2016
                : 31 January 2017
                : 6 February 2017
                Categories
                Article

                Oceanography & Hydrology
                nitrite,free nitrous acid,denitrification,paracoccus denitrificans,nitrosative stress,reactive nitrogen species,flavohemoglobin,nitric oxide

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