Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/31856

TítuloHalorhabdus tiamatea : proteogenomics and glycosidase activity measurements identify the first cultivated euryarchaeon from a deep-sea anoxic brine lake as potential polysaccharide degrader
Autor(es)Werner, Johannes
Ferrer, Manuel
Michel, Gurvan
Mann, Alexander J.
Sixing Huang
Juarez, Silvia
Ciordia, Sergio
Albar, Juan P.
Alcaide, María
La Cono, Violetta
Yakimov, Michail M.
Antunes, André Guimarães Lemos
Taborda, Marco
Costa, Milton S. da
Tran Hai
Glöckner, Frank Oliver
Golyshina, Olga V.
Golyshin, Peter N.
Teeling, Hanno
The MAMBA Consortium
Data2014
EditoraBlackwell Publishing Inc.
RevistaApplied and Environmental Microbiology
CitaçãoWerner, Johannes; Ferrer, Manuel; Michel, Gurvan; Mann, Alexander J.; Huang, Sixing; Juarez, Silvia; Ciordia, Sergio; Albar, Juan P.; Alcaide, María; La Cono, Violetta; Yakimov, Michail M.; Antunes, A.; Taborda, Marco; da Costa, Milton S.; Hai, Tran; Glöckner, Frank Oliver; Golyshina, Olga V.; Golyshin, Peter N.; Teeling, Hanno; The MAMBA Consortium, Halorhabdus tiamatea: proteogenomics and glycosidase activity measurements identify the first cultivated euryarchaeon from a deep-sea anoxic brine lake as potential polysaccharide degrader. Environmental Microbiology, 16(8), 2525-2537, 2014
Resumo(s)Euryarchaea from the genus Halorhabdus have been found in hypersaline habitats worldwide, yet are represented by only two isolates: Halorhabdus utahensis AX-2T from the shallow Great Salt Lake of Utah, and Halorhabdus tiamatea SARL4BT from the Shaban deep-sea hypersaline anoxic lake (DHAL) in the Red Sea. We sequenced the H. tiamatea genome to elucidate its niche adaptations. Among sequenced archaea, H. tiamatea features the highest number of glycoside hydrolases, the majority of which were expressed in proteome experiments. Annotations and glycosidase activity measurements suggested an adaptation towards recalcitrant algal and plant-derived hemicelluloses. Glycosidase activities were higher at 2% than at 0% or 5% oxygen, supporting a preference for low-oxygen conditions. Likewise, proteomics indicated quinone-mediated electron transport at 2% oxygen, but a notable stress response at 5% oxygen. Halorhabdus tiamatea furthermore encodes proteins characteristic for thermophiles and light-dependent enzymes (e.g. bacteriorhodopsin), suggesting that H. tiamatea evolution was mostly not governed by a cold, dark, anoxic deep-sea habitat. Using enrichment and metagenomics, we could demonstrate presence of similar glycoside hydrolase-rich Halorhabdus members in the Mediterranean DHAL Medee, which supports that Halorhabdus species can occupy a distinct niche as polysaccharide degraders in hypersaline environments.
TipoArtigo
URIhttps://hdl.handle.net/1822/31856
DOI10.1111/1462-2920.12393
ISSN1462-2912
e-ISSN1462-2920
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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