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1.
ISME J ; 12(4): 1163-1166, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-29382947

RESUMEN

Volatile organic compounds play an important role in microbial interactions. However, little is known about how volatile-mediated interactions modulate biogeochemical processes. In this study, we show the effect of volatile-mediated interaction on growth and functioning of aerobic methane-oxidizing bacteria, grown in co-culture with five different heterotrophs. Both growth and methane oxidation of Methylobacter luteus were stimulated by interaction with specific heterotrophs. In Methylocystis parvus, we observed significant growth promotion, while methane oxidation was inhibited. Volatolomics of the interaction of each of the methanotrophs with Pseudomonas mandelii, revealed presence of a complex blend of volatiles, including dimethylsulfide, dimethyldisulfide, and bicyclic sesquiterpenes. Although the ecological role of the detected compounds remains to be elucidated, our results provide unprecedented insights into interspecific relations and associated volatiles for stimulating methanotroph functioning, which is of substantial environmental and biotechnological significance.


Asunto(s)
Metano/metabolismo , Procesos Heterotróficos , Methylococcaceae/crecimiento & desarrollo , Methylococcaceae/metabolismo , Methylocystaceae/crecimiento & desarrollo , Methylocystaceae/metabolismo , Pseudomonas/metabolismo , Compuestos Orgánicos Volátiles/metabolismo
2.
Appl Environ Microbiol ; 53(2): 217-23, 1987 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16347270

RESUMEN

A method was developed to follow bacterial nitrate reduction in freshwater sediments by using common high-performance liquid chromatographic equipment. The low detection limit (14 pmol) of the method enabled us to study concentration profiles and reaction kinetics under natural conditions. Significant nitrate concentrations (1 to 27 muM) were observed in the sediment of Lake Vechten during the nonstratified period; the concentration profiles showed a successive depletion of oxygen, nitrate, and sulfate with depth. The profiles were restricted to the upper 3 cm of the sediment which is rich in organics and loosely structured. Nitrate reduction in the sediment-water interface followed first-order reaction kinetics at in situ concentrations. Remarkably high potential nitrate-reducing activity was observed in the part of the sediment in which nitrate did not diffuse. This activity was also observed throughout the whole year. Estimates of K(m) varied between 17 and 100 muM and V(max) varied between 7.2 and 36 mumol cm day for samples taken at different depths. The diffusion coefficient of nitrate ([10 +/- 0.4] x 10 cm s) across the sediment-water interface was estimated by a constant-source technique and applied to a mathematical model to estimate the net nitrate reduction during the nonstratified period. In this period, observed nitrate reduction rates by the model, 0.2 to 0.4 mmol m day, were lower than those found for oxygen (27 mmol m day) and sulfate (0.4 mmol m day). During the summer stratification, nitrate was absent in the sediment and reduction could not be estimated by the model.

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