Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon

Little is known about the methanogenic degradation of acetate, the fate of molecular hydrogen and formate or the ability of methanogens to grow and produce methane in cold, anoxic marine sediments. The microbes that produce methane were examined in permanently cold, anoxic marine sediments at Hy...

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Main Authors: Melissa M. Kendall, David R. Boone
Format: Article
Language:English
Published: Hindawi Limited 2006-01-01
Series:Archaea
Online Access:http://dx.doi.org/10.1155/2006/710190
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spelling doaj-e3aecc7d676f4d498c10315e283c47042021-07-02T10:29:47ZengHindawi LimitedArchaea1472-36461472-36542006-01-0121313810.1155/2006/710190Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, OregonMelissa M. Kendall0David R. Boone1Biology Department, Portland State University, P.O. Box 751, Portland, Oregon 97207–0751, USABiology Department, Portland State University, P.O. Box 751, Portland, Oregon 97207–0751, USALittle is known about the methanogenic degradation of acetate, the fate of molecular hydrogen and formate or the ability of methanogens to grow and produce methane in cold, anoxic marine sediments. The microbes that produce methane were examined in permanently cold, anoxic marine sediments at Hydrate Ridge (44°35' N, 125°10' W, depth 800 m). Sediment samples (15 to 35 cm deep) were collected from areas of active methane ebullition or areas where methane hydrates occurred. The samples were diluted into enrichment medium with formate, acetate or trimethylamine as catabolic substrate. After 2 years of incubation at 4 °C to 15 °C, enrichment cultures produced methane. PCR amplification and sequencing of the rRNA genes from the highest dilutions with growth suggested that each enrichment culture contained a single strain of methanogen. The level of sequence similarity (91 to 98%) to previously characterized prokaryotes suggested that these methanogens belonged to novel genera or species within the orders Methanomicrobiales and Methanosarcinales. Analysis of the 16S rRNA gene libraries from DNA extracted directly from the sediment samples revealed phylotypes that were either distantly related to cultivated methanogens or possible anaerobic methane oxidizers related to the ANME-1 and ANME-2 groups of the Archaea. However, no methanogenic sequences were detected, suggesting that methanogens represented only a small proportion of the archaeal community.http://dx.doi.org/10.1155/2006/710190
collection DOAJ
language English
format Article
sources DOAJ
author Melissa M. Kendall
David R. Boone
spellingShingle Melissa M. Kendall
David R. Boone
Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon
Archaea
author_facet Melissa M. Kendall
David R. Boone
author_sort Melissa M. Kendall
title Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon
title_short Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon
title_full Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon
title_fullStr Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon
title_full_unstemmed Cultivation of methanogens from shallow marine sediments at Hydrate Ridge, Oregon
title_sort cultivation of methanogens from shallow marine sediments at hydrate ridge, oregon
publisher Hindawi Limited
series Archaea
issn 1472-3646
1472-3654
publishDate 2006-01-01
description Little is known about the methanogenic degradation of acetate, the fate of molecular hydrogen and formate or the ability of methanogens to grow and produce methane in cold, anoxic marine sediments. The microbes that produce methane were examined in permanently cold, anoxic marine sediments at Hydrate Ridge (44°35' N, 125°10' W, depth 800 m). Sediment samples (15 to 35 cm deep) were collected from areas of active methane ebullition or areas where methane hydrates occurred. The samples were diluted into enrichment medium with formate, acetate or trimethylamine as catabolic substrate. After 2 years of incubation at 4 °C to 15 °C, enrichment cultures produced methane. PCR amplification and sequencing of the rRNA genes from the highest dilutions with growth suggested that each enrichment culture contained a single strain of methanogen. The level of sequence similarity (91 to 98%) to previously characterized prokaryotes suggested that these methanogens belonged to novel genera or species within the orders Methanomicrobiales and Methanosarcinales. Analysis of the 16S rRNA gene libraries from DNA extracted directly from the sediment samples revealed phylotypes that were either distantly related to cultivated methanogens or possible anaerobic methane oxidizers related to the ANME-1 and ANME-2 groups of the Archaea. However, no methanogenic sequences were detected, suggesting that methanogens represented only a small proportion of the archaeal community.
url http://dx.doi.org/10.1155/2006/710190
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