The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry

Many microorganisms feed on the tissue and recalcitrant bone materials from dead animals, however little is known about the collaborative effort and characteristics of their enzymes. In this study, microbial metagenomes from symbionts of the marine bone-dwelling worm Osedax mucofloris, and from micr...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Laura Fernandez-Lopez, Sergio Sanchez-Carrillo, Antonio García-Moyano, Erik Borchert, David Almendral, Sandra Alonso, Isabel Cea-Rama, Noa Miguez, Øivind Larsen, Johannes Werner, Kira S. Makarova, Francisco J. Plou, Thomas G. Dahlgren, Julia Sanz-Aparicio, Ute Hentschel, Gro Elin Kjæreng Bjerga, Manuel Ferrer
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://doaj.org/article/4d56ef80d0354f6c92a291c584168217
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:4d56ef80d0354f6c92a291c584168217
record_format dspace
spelling oai:doaj.org-article:4d56ef80d0354f6c92a291c5841682172021-12-02T05:00:24ZThe bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry2001-037010.1016/j.csbj.2021.11.027https://doaj.org/article/4d56ef80d0354f6c92a291c5841682172021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S200103702100492Xhttps://doaj.org/toc/2001-0370Many microorganisms feed on the tissue and recalcitrant bone materials from dead animals, however little is known about the collaborative effort and characteristics of their enzymes. In this study, microbial metagenomes from symbionts of the marine bone-dwelling worm Osedax mucofloris, and from microbial biofilms growing on experimentally deployed bone surfaces were screened for specialized bone-degrading enzymes. A total of 2,043 taxonomically (closest match within 40 phyla) and functionally (1 proteolytic and 9 glycohydrolytic activities) diverse and non-redundant sequences (median pairwise identity of 23.6%) encoding such enzymes were retrieved. The taxonomic assignation and the median identity of 72.2% to homologous proteins reflect microbial and functional novelty associated to a specialized bone-degrading marine community. Binning suggests that only one generalist hosting all ten targeted activities, working in synergy with multiple specialists hosting a few or individual activities. Collagenases were the most abundant enzyme class, representing 48% of the total hits. A total of 47 diverse enzymes, representing 8 hydrolytic activities, were produced in Escherichia coli, whereof 13 were soluble and active. The biochemical analyses revealed a wide range of optimal pH (4.0–7.0), optimal temperature (5–65 °C), and of accepted substrates, specific to each microbial enzyme. This versatility may contribute to a high environmental plasticity of bone-degrading marine consortia that can be confronted to diverse habitats and bone materials. Through bone-meal degradation tests, we further demonstrated that some of these enzymes, particularly those from Flavobacteriaceae and Marinifilaceae, may be an asset for development of new value chains in the biorefinery industry.Laura Fernandez-LopezSergio Sanchez-CarrilloAntonio García-MoyanoErik BorchertDavid AlmendralSandra AlonsoIsabel Cea-RamaNoa MiguezØivind LarsenJohannes WernerKira S. MakarovaFrancisco J. PlouThomas G. DahlgrenJulia Sanz-AparicioUte HentschelGro Elin Kjæreng BjergaManuel FerrerElsevierarticleBone microbiomeBone degradationCollagenaseGlycosidaseMetagenomicsOsedax mucoflorisBiotechnologyTP248.13-248.65ENComputational and Structural Biotechnology Journal, Vol 19, Iss , Pp 6328-6342 (2021)
institution DOAJ
collection DOAJ
language EN
topic Bone microbiome
Bone degradation
Collagenase
Glycosidase
Metagenomics
Osedax mucofloris
Biotechnology
TP248.13-248.65
spellingShingle Bone microbiome
Bone degradation
Collagenase
Glycosidase
Metagenomics
Osedax mucofloris
Biotechnology
TP248.13-248.65
Laura Fernandez-Lopez
Sergio Sanchez-Carrillo
Antonio García-Moyano
Erik Borchert
David Almendral
Sandra Alonso
Isabel Cea-Rama
Noa Miguez
Øivind Larsen
Johannes Werner
Kira S. Makarova
Francisco J. Plou
Thomas G. Dahlgren
Julia Sanz-Aparicio
Ute Hentschel
Gro Elin Kjæreng Bjerga
Manuel Ferrer
The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry
description Many microorganisms feed on the tissue and recalcitrant bone materials from dead animals, however little is known about the collaborative effort and characteristics of their enzymes. In this study, microbial metagenomes from symbionts of the marine bone-dwelling worm Osedax mucofloris, and from microbial biofilms growing on experimentally deployed bone surfaces were screened for specialized bone-degrading enzymes. A total of 2,043 taxonomically (closest match within 40 phyla) and functionally (1 proteolytic and 9 glycohydrolytic activities) diverse and non-redundant sequences (median pairwise identity of 23.6%) encoding such enzymes were retrieved. The taxonomic assignation and the median identity of 72.2% to homologous proteins reflect microbial and functional novelty associated to a specialized bone-degrading marine community. Binning suggests that only one generalist hosting all ten targeted activities, working in synergy with multiple specialists hosting a few or individual activities. Collagenases were the most abundant enzyme class, representing 48% of the total hits. A total of 47 diverse enzymes, representing 8 hydrolytic activities, were produced in Escherichia coli, whereof 13 were soluble and active. The biochemical analyses revealed a wide range of optimal pH (4.0–7.0), optimal temperature (5–65 °C), and of accepted substrates, specific to each microbial enzyme. This versatility may contribute to a high environmental plasticity of bone-degrading marine consortia that can be confronted to diverse habitats and bone materials. Through bone-meal degradation tests, we further demonstrated that some of these enzymes, particularly those from Flavobacteriaceae and Marinifilaceae, may be an asset for development of new value chains in the biorefinery industry.
format article
author Laura Fernandez-Lopez
Sergio Sanchez-Carrillo
Antonio García-Moyano
Erik Borchert
David Almendral
Sandra Alonso
Isabel Cea-Rama
Noa Miguez
Øivind Larsen
Johannes Werner
Kira S. Makarova
Francisco J. Plou
Thomas G. Dahlgren
Julia Sanz-Aparicio
Ute Hentschel
Gro Elin Kjæreng Bjerga
Manuel Ferrer
author_facet Laura Fernandez-Lopez
Sergio Sanchez-Carrillo
Antonio García-Moyano
Erik Borchert
David Almendral
Sandra Alonso
Isabel Cea-Rama
Noa Miguez
Øivind Larsen
Johannes Werner
Kira S. Makarova
Francisco J. Plou
Thomas G. Dahlgren
Julia Sanz-Aparicio
Ute Hentschel
Gro Elin Kjæreng Bjerga
Manuel Ferrer
author_sort Laura Fernandez-Lopez
title The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry
title_short The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry
title_full The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry
title_fullStr The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry
title_full_unstemmed The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry
title_sort bone-degrading enzyme machinery: from multi-component understanding to the treatment of residues from the meat industry
publisher Elsevier
publishDate 2021
url https://doaj.org/article/4d56ef80d0354f6c92a291c584168217
work_keys_str_mv AT laurafernandezlopez thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT sergiosanchezcarrillo thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT antoniogarciamoyano thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT erikborchert thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT davidalmendral thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT sandraalonso thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT isabelcearama thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT noamiguez thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT øivindlarsen thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT johanneswerner thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT kirasmakarova thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT franciscojplou thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT thomasgdahlgren thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT juliasanzaparicio thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT utehentschel thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT groelinkjærengbjerga thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT manuelferrer thebonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT laurafernandezlopez bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT sergiosanchezcarrillo bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT antoniogarciamoyano bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT erikborchert bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT davidalmendral bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT sandraalonso bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT isabelcearama bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT noamiguez bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT øivindlarsen bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT johanneswerner bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT kirasmakarova bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT franciscojplou bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT thomasgdahlgren bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT juliasanzaparicio bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT utehentschel bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT groelinkjærengbjerga bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
AT manuelferrer bonedegradingenzymemachineryfrommulticomponentunderstandingtothetreatmentofresiduesfromthemeatindustry
_version_ 1718400827203256320