Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases

Abstract In the present study we investigate the microbial community inhabiting As Burgas geothermal spring, located in Ourense (Galicia, Spain). The approximately 23 Gbp of Illumina sequences generated for each replicate revealed a complex microbial community dominated by Bacteria in which Proteoba...

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Autores principales: María-Eugenia DeCastro, Michael P. Doane, Elizabeth Ann Dinsdale, Esther Rodríguez-Belmonte, María-Isabel González-Siso
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/dedbadce5f1b41e9967159b1694085e0
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spelling oai:doaj.org-article:dedbadce5f1b41e9967159b1694085e02021-12-02T15:08:22ZExploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases10.1038/s41598-020-80489-62045-2322https://doaj.org/article/dedbadce5f1b41e9967159b1694085e02021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-80489-6https://doaj.org/toc/2045-2322Abstract In the present study we investigate the microbial community inhabiting As Burgas geothermal spring, located in Ourense (Galicia, Spain). The approximately 23 Gbp of Illumina sequences generated for each replicate revealed a complex microbial community dominated by Bacteria in which Proteobacteria and Aquificae were the two prevalent phyla. An association between the two most prevalent genera, Thermus and Hydrogenobacter, was suggested by the relationship of their metabolism. The high relative abundance of sequences involved in the Calvin–Benson cycle and the reductive TCA cycle unveils the dominance of an autotrophic population. Important pathways from the nitrogen and sulfur cycle are potentially taking place in As Burgas hot spring. In the assembled reads, two complete ORFs matching GH2 beta-galactosidases were found. To assess their functional characterization, the two ORFs were cloned and overexpressed in E. coli. The pTsbg enzyme had activity towards o-Nitrophenyl-β-d-galactopyranoside (ONPG) and p-Nitrophenyl-β-d-fucopyranoside, with high thermal stability and showing maximal activity at 85 °C and pH 6, nevertheless the enzyme failed to hydrolyze lactose. The other enzyme, Tsbg, was unable to hydrolyze even ONPG or lactose. This finding highlights the challenge of finding novel active enzymes based only on their sequence.María-Eugenia DeCastroMichael P. DoaneElizabeth Ann DinsdaleEsther Rodríguez-BelmonteMaría-Isabel González-SisoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
María-Eugenia DeCastro
Michael P. Doane
Elizabeth Ann Dinsdale
Esther Rodríguez-Belmonte
María-Isabel González-Siso
Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases
description Abstract In the present study we investigate the microbial community inhabiting As Burgas geothermal spring, located in Ourense (Galicia, Spain). The approximately 23 Gbp of Illumina sequences generated for each replicate revealed a complex microbial community dominated by Bacteria in which Proteobacteria and Aquificae were the two prevalent phyla. An association between the two most prevalent genera, Thermus and Hydrogenobacter, was suggested by the relationship of their metabolism. The high relative abundance of sequences involved in the Calvin–Benson cycle and the reductive TCA cycle unveils the dominance of an autotrophic population. Important pathways from the nitrogen and sulfur cycle are potentially taking place in As Burgas hot spring. In the assembled reads, two complete ORFs matching GH2 beta-galactosidases were found. To assess their functional characterization, the two ORFs were cloned and overexpressed in E. coli. The pTsbg enzyme had activity towards o-Nitrophenyl-β-d-galactopyranoside (ONPG) and p-Nitrophenyl-β-d-fucopyranoside, with high thermal stability and showing maximal activity at 85 °C and pH 6, nevertheless the enzyme failed to hydrolyze lactose. The other enzyme, Tsbg, was unable to hydrolyze even ONPG or lactose. This finding highlights the challenge of finding novel active enzymes based only on their sequence.
format article
author María-Eugenia DeCastro
Michael P. Doane
Elizabeth Ann Dinsdale
Esther Rodríguez-Belmonte
María-Isabel González-Siso
author_facet María-Eugenia DeCastro
Michael P. Doane
Elizabeth Ann Dinsdale
Esther Rodríguez-Belmonte
María-Isabel González-Siso
author_sort María-Eugenia DeCastro
title Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases
title_short Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases
title_full Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases
title_fullStr Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases
title_full_unstemmed Exploring the taxonomical and functional profile of As Burgas hot spring focusing on thermostable β-galactosidases
title_sort exploring the taxonomical and functional profile of as burgas hot spring focusing on thermostable β-galactosidases
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/dedbadce5f1b41e9967159b1694085e0
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