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1.
Environ Microbiol Rep ; 5(3): 414-23, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23754722

RESUMEN

Diverse copper-containing membrane-bound monooxygenase-encoding sequences (Cu-MMOs) have recently been described from the marine environment, suggesting widespread potential for oxidation of reduced substrates. Here, we used the well-defined oxygen and methane gradients associated with the Costa Rican oxygen minimum zone (OMZ) to gain insight into the physico-chemical parameters influencing the distribution and abundance of Cu-MMO-encoding marine microorganisms. Two Methylococcales-related Cu-MMO-encoding lineages, termed groups OPU1 and OPU3, demonstrated differences in their relative abundance, with both pmoA and candidate 16S rRNA genes correlating significantly with reduced environmental oxygen concentrations and depth. In contrast, a newly identified Cu-MMO-encoding lineage, Group C, was primarily associated with the oxygenated euphotic zone. An updated phylogenetic analysis including these sequences, a marine pxmABC gene cluster, ethylene-utilizing Cu-MMO-encoding lineages and previously reported planktonic Cu-MMOs (Groups W, X, Z and O) demonstrates the breadth of diversity of Cu-MMO-encoding marine microorganisms. Groups C and X affiliated phylogenetically with ethane- and ethylene-oxidizing Cu-MMOs, Groups W and O affiliated phylogenetically with the recently described Cu-MMO 'pXMO', and Group Z clustered with Cu-MMOs recovered from soils. Collectively, these data demonstrate widespread genetic potential in ocean waters for the oxidation of small, reduced molecules and advance our understanding of the microorganisms involved in methane cycling in the OMZ environment.


Asunto(s)
Proteínas Bacterianas/genética , Metano/metabolismo , Methylococcaceae/genética , Oxigenasas de Función Mixta/genética , Oxígeno/metabolismo , ARN Ribosómico 16S/genética , Agua de Mar/microbiología , Proteínas Bacterianas/metabolismo , Membrana Celular/metabolismo , Cobre/química , Cobre/metabolismo , Costa Rica , Genes de ARNr , Variación Genética , Methylococcaceae/enzimología , Oxigenasas de Función Mixta/clasificación , Oxigenasas de Función Mixta/metabolismo , Oxidación-Reducción , Filogenia , Unión Proteica , ARN Ribosómico 16S/clasificación
2.
Biophys J ; 79(2): 1085-94, 2000 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-10920038

RESUMEN

X-band (9.1 GHz) and S-band (3.4 GHz) electron paramagnetic resonance (EPR) spectra for particulate methane monooxygenase (pMMO) in whole cells from Methylococcus capsulatus (Bath) grown on (63)Cu and (15)N were obtained and compared with previously reported spectra for pMMO from Methylomicrobium album BG8. For both M. capsulatus (Bath) and M. album BG8, two nearly identical Cu(2+) EPR signals with resolved hyperfine coupling to four nitrogens are observed. The EPR parameters for pMMO from M. capsulatus (Bath) (g( parallel) = 2.244, A( parallel) = 185 G, and A(N) = 19 G for signal one; g( parallel) = 2.246, A( parallel) = 180 G, and A(N) = 19 G for signal two) and for pMMO from M. album BG8 (g( parallel) = 2.243, A( parallel) = 180 G, and A(N) = 18 G for signal one; g( parallel) = 2. 251, A( parallel) = 180 G, and A(N) = 18 G for signal two) are very similar and are characteristic of type 2 Cu(2+) in a square planar or square pyramidal geometry. In three-pulse electron spin echo envelope modulation (ESEEM) data for natural-abundance samples, nitrogen quadrupolar frequencies due to the distant nitrogens of coordinated histidine imidazoles were observed. The intensities of the quadrupolar combination bands indicate that there are three or four coordinated imidazoles, which implies that most, if not all, of the coordinated nitrogens detected in the continuous wave spectra are from histidine imidazoles.


Asunto(s)
Cobre/metabolismo , Methylococcaceae/enzimología , Methylococcus capsulatus/enzimología , Oxigenasas/química , Sitios de Unión , Espectroscopía de Resonancia por Spin del Electrón/métodos , Metaloproteínas/química , Metaloproteínas/metabolismo , Oxigenasas/metabolismo , Conformación Proteica
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