scholarly journals Immobilized protease on magnetic particles for enzymatic protein hydrolysis of poultry by-products

LWT ◽  
2021 ◽  
Vol 152 ◽  
pp. 112327
Author(s):  
Wilhelm R. Glomm ◽  
Sileshi G. Wubshet ◽  
Diana Lindberg ◽  
Katinka R. Dankel ◽  
Nils K. Afseth ◽  
...  
2017 ◽  
Vol 9 (29) ◽  
pp. 4247-4254 ◽  
Author(s):  
Sileshi Gizachew Wubshet ◽  
Ingrid Måge ◽  
Ulrike Böcker ◽  
Diana Lindberg ◽  
Svein Halvor Knutsen ◽  
...  

An FTIR-based multivariate approach is developed for monitoring molecular weight distribution during enzymatic protein hydrolysis of byproducts.


Author(s):  
Sileshi G. Wubshet ◽  
Diana Lindberg ◽  
Eva Veiseth-Kent ◽  
Kenneth A. Kristoffersen ◽  
Ulrike Böcker ◽  
...  

2018 ◽  
Vol 11 (11) ◽  
pp. 2032-2043 ◽  
Author(s):  
Sileshi Gizachew Wubshet ◽  
Jens Petter Wold ◽  
Nils Kristian Afseth ◽  
Ulrike Böcker ◽  
Diana Lindberg ◽  
...  

2018 ◽  
Vol 54 (4A) ◽  
pp. 140
Author(s):  
Tran Chi Linh

Protein hydrolysates were produced from shrimp waste mainly comprising head and shell by different commercial proteases (Alcalase, Protamex, Flavourzyme). Shrimp waste was mixed with water (ratio of 1:5 w/v) and was treated with protease individually or together, which were incorporated either simultaneously or sequentially. Temperature was kept at the optimum for each enzyme. pH was initially adjusted to the most favorable value for each enzyme. Result of study showed that in case of individial addition, the highest yield of protein recovery (YPR 48.88 %) was obtained with Alcalase (375 U/g material) at 50 °C, pH 8 for 4 hours. Besides, the maximal yield of amino acids recovery (2.91 %) was obtained with Flavourzyme (250 U/g material) at 50 °C, pH 7 for 4 hours. Specially, the sequential treatment with Alcalase and Flavourzyme improved significantly the hydrolysis of protein. The yield of protein recovery (YPR 49.13 %) and yield of amino acids recovery (YAR 6.91 %) were obtained by addition of Flavourzyme 6 hours after Alcalase, which is attributed to the combined nature of the endo- and exocatalytic action of Alcalase and Flavourzyme, respectively. This research shows the feasibility of hydrolyzing shrimp by-products using different commercial proteases.


2020 ◽  
Vol 849 ◽  
pp. 72-77
Author(s):  
Firman Kurniawansyah ◽  
Amila D. Istiqomah ◽  
Aisyah J. Malahayati ◽  
Himawan Tri Bayu Murti Petrus ◽  
Achmad Roesyadi

Synthesizing materials can be attempted by utilizing alternative sources such as wastes or disposed/by-products of certain activities. In this article, exploration of silica from agricultural waste and from geothermal sludgefor production of silica catalysts, are presented. The first silica catalyst was synthesized from rice husk. The husk was initially heated until silica ashes could be formed. After immersion in acidic solution, impregnation with nickel and molybdenum were conducted to introduce active metal of nickel (Ni) and molybdenum (Mo) in the support structure. The catalyst formed, Ni-Mo/SiO2 was applied to convert crude palm oil into biofuels. The other silica catalyst was obtained from geothermal sludge. After washing, the catalyst was soaked in sulphuric acid solution to form acidic silica solid catalyst. The catalyst was applied in hydrolysis of seaweed-industry solid waste to produce glucose. The catalyst was relatively successful to facilitate 19-20% glucose yield, or up to 21% glucose selectivity from waste material.


2014 ◽  
Vol 40 (2) ◽  
pp. 103-113
Author(s):  
Marcin Wołczyński ◽  
Marta Janosz-Rajczyk

Abstract The presented results of research on the effectiveness of enzymatic hydrolysis of lignocellulosic waste, depending on their initial depolymerisation in alkaline medium were considered in the context of the possibility of their further use in the fermentation media focused on the recovery of energy in the form of molecular hydrogen. The aim of this study was to determine the appropriate dose and concentration of a chemical reagent, whose efficiency would be high enough to cause decomposition of the complex, but without an excessive production of by-products which could adversely affect the progress and effectiveness of the enzymatic hydrolysis and fermentation. The effect of treatment on physical-chemical changes of homogenates’ properties such as pH, COD, the concentration of monosaccharide and total sugars and the concentration of total suspended solids and volatile suspended solids was determined. The enzymatic decomposition of lignocellulosic complex was repeatedly more efficient if the sample homogenates were subjected to an initial exposure to NaOH. The degree of conversion of complex sugars into simple sugars during enzymatic hydrolysis of homogenates pre-alkalized to pH 11.5 and 12.0 was 83.3 and 84.2% respectively, which should be sufficient for efficient hydrogen fermentation process.


2009 ◽  
Vol 18 (1-2) ◽  
pp. 120-134 ◽  
Author(s):  
Irineu Batista ◽  
Cristina Ramos ◽  
Rita Mendonça ◽  
Maria Leonor Nunes

2016 ◽  
Vol 71 (3) ◽  
pp. 249-265 ◽  
Author(s):  
Christina Taouss ◽  
Peter G. Jones

AbstractDiphosphanegold(I) complexes of the form dppmEAuX [dppm = bis(diphenylphosphano)methane, E = S, Se; X = Br, I], dppeEAuX [dppe = 1,2-bis(diphenylphosphano)ethane; E = O, S; X = Br, I] and dppbzEAuX [dppbz = 1,2-bis(diphenylphosphano)benzene; E = S, Se, X = Br, I] were treated with elemental X2. With dppm, the three products [dppmEAuX2]+X3– (E = S, X = Br (1), I (2); E = Se, X = I (3) were obtained in quantitative yield. These are gold(III) complexes involving a five-membered ring . With dppe, the only related product was [dppeEAuBr2]+Br3– (4), in which the central ring is six-membered with two carbon atoms. These dppe systems are very sensitive to oxidation/hydrolysis of the ligand, and several such unintended products were isolated and identified. The reaction of dppbzSAuBr with bromine leads to [dppbzS]2+[AuBr4]–Br– (5), the dication of which is formally 1,1,3,3-tetraphenylbenzo[d]-2-thia-1, 3-diphosphol-1,3-diium and contains a central five-membered ring . The dications are associated with the bromide anions via S…Br contacts of ca. 3.1 Å to form inversion-symmetric S2Br2 rings. The halogenation of the dppbzSe derivatives leads to loss of selenium and formation of dppbzAuBr3 (6), with [4+1] coordination at gold, or the known compound [dppbzAuI2]+I3– (7). All products 1–6 were subjected to X-ray diffraction analyses, as were four hydrolysis products 4a–d and two further by-products [5(thtBr+)·2Br3–·3(AuBr4–)] (1a) and (tht)AuBr3 (1b). Compound 1a displays unusually short Br…Br contacts of 3.2398(8) Å between neighbouring tetrabromidoaurate(III) ions.


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