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dc.contributor.authorWohlgemuth, R
dc.contributor.authorLittlechild, J
dc.contributor.authorMonti, D
dc.contributor.authorSchnorr, K
dc.contributor.authorvan Rossum, T
dc.contributor.authorSiebers, B
dc.contributor.authorMenzel, P
dc.contributor.authorKublanov, IV
dc.contributor.authorRike, AG
dc.contributor.authorSkretas, G
dc.contributor.authorSzabo, Z
dc.contributor.authorPeng, X
dc.contributor.authorYoung, MJ
dc.date.accessioned2020-01-23T12:09:30Z
dc.date.issued2018-09-25
dc.description.abstractNovel hydrolases from hot and other extreme environments showing appropriate performance and/or novel functionalities and new approaches for their systematic screening are of great interest for developing new processes, for improving safety, health and environment issues. Existing processes could benefit as well from their properties. The workflow, based on the HotZyme project, describes a multitude of technologies and their integration from discovery to application, providing new tools for discovering, identifying and characterizing more novel thermostable hydrolases with desired functions from hot terrestrial and marine environments. To this end, hot springs worldwide were mined, resulting in hundreds of environmental samples and thousands of enrichment cultures growing on polymeric substrates of industrial interest. Using high-throughput sequencing and bioinformatics, 15 hot spring metagenomes, as well as several sequenced isolate genomes and transcriptomes were obtained. To facilitate the discovery of novel hydrolases, the annotation platform Anastasia and a whole-cell bioreporter-based functional screening method were developed. Sequence-based screening and functional screening together resulted in about 100 potentially new hydrolases of which more than a dozen have been characterized comprehensively from a biochemical and structural perspective. The characterized hydrolases include thermostable carboxylesterases, enol lactonases, quorum sensing lactonases, gluconolactonases, epoxide hydrolases, and cellulases. Apart from these novel thermostable hydrolases, the project generated an enormous amount of samples and data, thereby allowing the future discovery of even more novel enzymes.en_GB
dc.description.sponsorshipEuropean Commissionen_GB
dc.description.sponsorshipEuropean Union FP7en_GB
dc.identifier.citationVol. 36 (8), pp. 2077 - 2100en_GB
dc.identifier.doi10.1016/j.biotechadv.2018.09.004
dc.identifier.grantnumberKBBE-2010-4-265933en_GB
dc.identifier.grantnumber265933en_GB
dc.identifier.urihttp://hdl.handle.net/10871/40546
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights© 2018. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dc.subjectHydrolasesen_GB
dc.subjectMetagenomicsen_GB
dc.subjectEnrichmenten_GB
dc.subjectSequencingen_GB
dc.subjectGenomicsen_GB
dc.subjectThermophilesen_GB
dc.subjectGene expressionen_GB
dc.subjectEnzyme screeningen_GB
dc.subjectEnzyme characterizationen_GB
dc.subjectBiocatalysisen_GB
dc.titleDiscovering novel hydrolases from hot environmentsen_GB
dc.typeArticleen_GB
dc.date.available2020-01-23T12:09:30Z
dc.identifier.issn0734-9750
dc.descriptionThis is the author accepted manuscript. The final version is available from Elsevier via the DOI in this recorden_GB
dc.identifier.journalBiotechnology Advancesen_GB
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dcterms.dateAccepted2018-09-24
exeter.funder::European Commissionen_GB
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2018-09-25
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-01-23T12:06:59Z
refterms.versionFCDAM
refterms.dateFOA2020-01-23T12:09:38Z
refterms.panelAen_GB


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© 2018. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  
Except where otherwise noted, this item's licence is described as © 2018. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/