Denitrifying metabolism of the methylotrophic marine bacterium Methylophaga nitratireducenticrescens strain JAM1

被引:12
作者
Mauffrey, Florian [1 ,2 ]
Cucaita, Alexandra [1 ]
Constant, Philippe [1 ]
Villemur, Richard [1 ]
机构
[1] INRS Inst Armand Frappier, Laval, PQ, Canada
[2] Lab Sante Publ Quebec, Ste Anne De Bellevue, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Denitrification; Marine bacterium; Methylophaga; Nitrous oxide; Nitrate; NITROUS-OXIDE PRODUCTION; DENITRIFICATION SYSTEM; NITRIC-OXIDE; METHYLOTENERA-MOBILIS; SP-NOV; DIVERSITY; NITRATE; REDUCTION; BIOFILM; OXIDATION;
D O I
10.7717/peerj.4098
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background. Methylophaga nitratireducenticrescens strain JAM1 is a methylotrophic, marine bacterium that was isolated from a denitrification reactor treating a closed-circuit seawater aquarium. It can sustain growth under anoxic conditions by reducing 3 nitrate (NO3-) to nitrite (NO2-). These physiological traits are attributed to gene clusters that encode two dissimilatory nitrate reductases (Nar). Strain JAM1 also contains gene clusters encoding two nitric oxide (NO) reductases and one nitrous oxide (N2O) reductase, suggesting that NO and N2O can be reduced by strain JAM1. Here we characterized further the denitrifying activities of M. nitratireducenticrescens JAM1. Methods. Series of oxic and anoxic cultures of strain JAM1 were performed with N2O, NO3- or sodium nitroprusside, and growth and N2O, NOT, NO2 and N-2 concentrations were measured. Ammonium (NH4+)-free cultures were also tested to assess the dynamics of N2O, NO3- and NO2. Isotopic labeling of N2O was performed in (NH4+)-N-15 -amended cultures. Cultures with the JAM1 A narGlnarG2 double mutant were performed to assess the involvement of the Nar systems on N2O production. Finally, RT-qPCR was used to measure the gene expression levels of the denitrification genes cytochrome bc-type nitric oxide reductase (cnorBl and cnorB2) and nitrous oxide reductase (nosZ), and also nnrS and norR that encode NO-sensitive regulators. Results. Strain JAM1 can reduce NO to N2O and N2O to N-2 and can sustain growth under anoxic conditions by reducing N2O as the sole electron acceptor. Although strain JAM1 lacks a gene encoding a dissimilatory NO2 reductase, NO(3)(-)amended cultures produce N2O, representing up to 6% of the N-input. NO2 was shown to be the key intermediate of this production process. Upregulation in the expression of cnorBl, cnorB2, nnrS and norR during the growth and the N2O accumulation phases suggests NO production in strain JAM1 cultures. Discussion. By showing that all the three denitrification reductases are active, this demonstrates that M nitratireducenticrescens JAM1 is one of many bacteria species that maintain genes associated primarily with denitrification, but not necessarily related to the maintenance of the entire pathway. The reason to maintain such an incomplete pathway could be related to the specific role of strain JAM1 in the denitrifying biofilm of the denitrification reactor from which it originates. The production of N2O in strain JAM1 did not involve Nar, contrary to what was demonstrated in Escherichia coli, M. nitratireducenticrescens JAM1 is the only reported Methylophaga species that has the capacity to grow under anoxic conditions by using NO3- and N2O as sole electron acceptors for its growth. It is also one of a few marine methylotrophs that is studied at the physiological and genetic levels in relation to its capacity to perform denitrifying activities.
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