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dc.contributor.authorMekasha, Sophanit
dc.contributor.authorByman, Ida Roksvåg
dc.contributor.authorLynch, Catherine
dc.contributor.authorToupalová, Hana
dc.contributor.authorAndera, Ladislav
dc.contributor.authorNæs, Tormod
dc.contributor.authorVaaje-Kolstad, Gustav
dc.contributor.authorEijsink, Vincentius Gerardus Henricus
dc.date.accessioned2018-04-17T10:59:54Z
dc.date.available2018-04-17T10:59:54Z
dc.date.created2017-05-30T11:25:22Z
dc.date.issued2017
dc.identifier.citationProcess Biochemistry. 2017, 56 132-138.
dc.identifier.issn1359-5113
dc.identifier.urihttp://hdl.handle.net/11250/2494448
dc.description.abstractOne potential strategy for biorefining of chitin-rich biomass entails enzymatic saccharification, which, so far, has been scarcely explored. Here, saccharification of chitin was explored using response surface methodology available in the MODDE®10 software, to develop optimal cocktails of five mono-component enzymes from Serratia marcescens, three chitinases, SmChiA, SmChiB, SmChiC, a lytic polysaccharide monooxygenase, SmLPMO10A (or “CBP21”), and a beta-N-acetylhexosaminidase, SmCHB (“chitobiase”). These five enzymes were recombinantly produced in Escherichia coli. For both shrimp and crab chitins, SmChiA was the most abundant (40% and 38%, respectively) in the optimized cocktails, whereas SmChiB, SmChiC and SmLPMO10A were present at 30% and 26%, 15% and 23%, and 3% and 2%, respectively. Saccharification yields were 70%–75%, whereas a “minimal” cocktail of SmChiA and SmCHB gave only 40% saccharification. These results show that enzymatic saccharification of chitin requires multiple enzyme activities applied at dosages similar to those used for saccharification of cellulose.
dc.language.isoeng
dc.titleDevelopment of enzyme cocktails for complete saccharification of chitin using mono-component enzymes from Serratia marcescens
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionacceptedVersion
dc.source.pagenumber132-138
dc.source.volume56
dc.source.journalProcess Biochemistry
dc.identifier.doi10.1016/j.procbio.2017.02.021
dc.identifier.cristin1472737
dc.relation.projectNofima AS: 201702
dc.relation.projectNorges forskningsråd: 262308
dc.relation.projectNorges forskningsråd: 221576
dc.relation.projectEC/FP7/FPR7-289284
cristin.unitcode7543,3,2,0
cristin.unitnameRåvare og prosess
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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