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Oxidation-reduction potential (ORP) as a tool for process monitoring of H2O2/LPMO assisted enzymatic hydrolysis of cellulose

Kadić, A. (författare)
Lund University,Lunds universitet,Avdelningen för kemiteknik,Institutionen för processteknik och tillämpad biovetenskap,Institutioner vid LTH,Lunds Tekniska Högskola,Division of Chemical Engineering,Department of Process and Life Science Engineering,Departments at LTH,Faculty of Engineering, LTH
Chylenski, P. (författare)
Norwegian University of Life Sciences
Tengstedt Hansen, Mads Anders (författare)
Borregaard AS
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Bengtsson, O. (författare)
Borregaard AS
Eijsink, Vincent G.H. (författare)
Norwegian University of Life Sciences
Lidén, Gunnar (författare)
Lund University,Lunds universitet,Avdelningen för kemiteknik,Institutionen för processteknik och tillämpad biovetenskap,Institutioner vid LTH,Lunds Tekniska Högskola,Division of Chemical Engineering,Department of Process and Life Science Engineering,Departments at LTH,Faculty of Engineering, LTH
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 (creator_code:org_t)
Elsevier BV, 2019
2019
Engelska.
Ingår i: Process Biochemistry. - : Elsevier BV. - 1359-5113. ; 86, s. 89-97
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Oxidation-reduction potential (ORP) is an environmental factor of importance in several biological conversion processes. Lytic polysaccharide monooxygenases (LPMOs) catalyze oxidative disruption of the cellulose chain in the presence of oxygen or hydrogen peroxide and increase enzymatic hydrolysis yields. However, the enzymes are also sensitive to oxidative damage and the level of oxidative agent needs to be controlled to avoid inactivation of the LPMOs. In the current study, enzymatic hydrolysis of sulfite-pretreated softwood (12% DM loading) was carried out in lab scale reactors with gradual addition of hydrogen peroxide using an LPMO-containing commercial enzyme cocktail. The ORP was measured during enzymatic hydrolysis together with released glucose and the level of C4-oxidized dimer as a marker for LPMO activity. Arrests in LPMO activity coincided with a markedly changed ORP signal and this was utilized in subsequent experiments in which the feed rate of hydrogen peroxide was controlled by keeping the ORP at predetermined set-points of -40 mV, -80 mV and -120 mV. Under anaerobic conditions, the highest hydrolysis yield (78% after 72 h) was found for the ORP set-point of -80 mV. The results show that ORP can serve as an indicator of LPMO activity and may help optimizing overall process efficiency.

Ämnesord

TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Biokatalys och enzymteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Biocatalysis and Enzyme Technology (hsv//eng)

Nyckelord

Cellulose
Enzymatic hydrolysis
Hydrogen peroxide
Lytic polysaccharide monooxygenase (LPMO)
Oxidation-reduction potential (ORP)
Redox

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