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Lignin enrichment and enzyme deactivation as the root cause of enzymatic hydrolysis slowdown of steam pretreated sugarcane bagasse

dc.contributor.authorWallace, Joshua
dc.contributor.authorBrienzo, Michel
dc.contributor.authorGarcia-Aparicio, Maria P.
dc.contributor.authorGoergens, Johann F.
dc.contributor.institutionUniv Stellenbosch
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-11-26T15:29:13Z
dc.date.available2018-11-26T15:29:13Z
dc.date.issued2016-05-25
dc.description.abstractThe enzymatic hydrolysis (EH) rate normally decreases during the hydrolysis, leaving unhydrolyzed material as residue. This phenomenon occurs during the hydrolysis of both cellulose (avicel) and lignocellulosic material, in nature or even pretreated. The progression of EH of steam pretreated sugarcane bagasse was associated with an initial (fast), intermediate (slower) and recalcitrant (slowest) phases, at glucan to glucose conversion yields of 61.7, 81.6 and 86%, respectively. Even though the EH of avicel as a simpler material than steam pretreated sugarcane bagasse, EH slowdown was present. The less thermo-stable endo-xylanase lost 58% of initial enzyme activity, followed by beta-glucosidase that lost 16%, culminating in FPase activity loss of 30% in the first 24 hours. After 72 hours of EH the total loss of FPase activity was 40% compared to the initial activity. Analysis of the solid residue from EH showed that lignin content, phenolic compounds and ash increased while glucan decreased as hydrolysis progressed. During the initial fast phase of EH, the total solid residue surface area consisted predominantly of internal surface area. Thereafter, in the intermediate and recalcitrant phases of EH, the ratio of external:internal surface area increased. The proposed fiber damage and decrease in internal surface area, probably by EH action, was visualized by scanning electron microscopy imagery. The higher lignin/glucan ratio as EH progressed and enzyme deactivation by thermo instability were the main effects observed, respectively to substrate and enzyme.en
dc.description.affiliationUniv Stellenbosch, Dept Proc Engn, Private Bag X1, ZA-7602 Stellenbosch, South Africa
dc.description.affiliationUniv Stellenbosch, Dept Microbiol, Private Bag X1, ZA-7602 Stellenbosch, South Africa
dc.description.sponsorshipSouth Africa Sugarcane Research Institute (SASRI)
dc.description.sponsorshipNational Research Foundation (NRF)
dc.description.sponsorshipTechnology and Human Resources for Industry Program of the Department of Trade and Industry of South Africa (DTI)
dc.format.extent361-371
dc.identifierhttp://dx.doi.org/10.1016/j.nbt.2016.01.004
dc.identifier.citationNew Biotechnology. Amsterdam: Elsevier Science Bv, v. 33, n. 3, p. 361-371, 2016.
dc.identifier.doi10.1016/j.nbt.2016.01.004
dc.identifier.fileWOS000373545600006.pdf
dc.identifier.issn1871-6784
dc.identifier.lattes8251885707409794
dc.identifier.urihttp://hdl.handle.net/11449/158796
dc.identifier.wosWOS:000373545600006
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofNew Biotechnology
dc.relation.ispartofsjr0,967
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.titleLignin enrichment and enzyme deactivation as the root cause of enzymatic hydrolysis slowdown of steam pretreated sugarcane bagasseen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.advisor.lattes8251885707409794
unesp.author.orcid0000-0002-3096-8843[2]

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