Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes

In the present study, hydrolysed protein of viscera and head of Silver carp (Hypophthalmichthys molitrix) was compared using Alcalase enzyme and internal tissue enzymes at 2 and 4 hours. The result indicated that product by Alcalase (Treatment 1) had significantly higher protein and rate of hydrolysates than that produced by internal tissue enzymes (Treatment 2). So, the highest mean (±SD) protein (68.10±1.33) was related to treatment 1-head (with Alcalase enzyme) after 4 hours and the highest rate of hydrolysates (29.36±1.35) was related to treatment 1-head (with Alcalase enzyme) after 4 hours. The result indicated that rate of hydrolysates raised as time of hydrolysates increased. However the intensity and rate of hydrolysates is reduced. The highest rate of hydrolysates occurred at 120 minutes in the first. This mode was similar for two treatments. The result can be considered as the Alcalase was preferred to internal enzyme.

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Bibliographic Details
Main Authors: Hosseini, Sh., Ghoroghi, A., Jamalzadeh, H.R., Safari, R.
Format: Journal Contribution biblioteca
Language:other
Published: 2012
Subjects:Processing, Hypophthalmichthys molitrix, Silver carp, Biotechnology, Fish, Comparison, Protein, Enzyme, Tissues,
Online Access:http://hdl.handle.net/1834/10635
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spelling dig-aquadocs-1834-106352021-05-19T06:45:25Z Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes Hosseini, Sh. Ghoroghi, A. Jamalzadeh, H.R. Safari, R. Hosseini, Sh. Processing Hypophthalmichthys molitrix Silver carp Biotechnology Fish Comparison Protein Enzyme Tissues In the present study, hydrolysed protein of viscera and head of Silver carp (Hypophthalmichthys molitrix) was compared using Alcalase enzyme and internal tissue enzymes at 2 and 4 hours. The result indicated that product by Alcalase (Treatment 1) had significantly higher protein and rate of hydrolysates than that produced by internal tissue enzymes (Treatment 2). So, the highest mean (±SD) protein (68.10±1.33) was related to treatment 1-head (with Alcalase enzyme) after 4 hours and the highest rate of hydrolysates (29.36±1.35) was related to treatment 1-head (with Alcalase enzyme) after 4 hours. The result indicated that rate of hydrolysates raised as time of hydrolysates increased. However the intensity and rate of hydrolysates is reduced. The highest rate of hydrolysates occurred at 120 minutes in the first. This mode was similar for two treatments. The result can be considered as the Alcalase was preferred to internal enzyme. Published 2017-11-29T17:52:37Z 2017-11-29T17:52:37Z 2012 Journal Contribution Refereed 1026-1354 http://hdl.handle.net/1834/10635 other pp.55-62 Iran
institution UNESCO
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-aquadocs
tag biblioteca
region Europa del Oeste
libraryname Repositorio AQUADOCS
language other
topic Processing
Hypophthalmichthys molitrix
Silver carp
Biotechnology
Fish
Comparison
Protein
Enzyme
Tissues
Processing
Hypophthalmichthys molitrix
Silver carp
Biotechnology
Fish
Comparison
Protein
Enzyme
Tissues
spellingShingle Processing
Hypophthalmichthys molitrix
Silver carp
Biotechnology
Fish
Comparison
Protein
Enzyme
Tissues
Processing
Hypophthalmichthys molitrix
Silver carp
Biotechnology
Fish
Comparison
Protein
Enzyme
Tissues
Hosseini, Sh.
Ghoroghi, A.
Jamalzadeh, H.R.
Safari, R.
Hosseini, Sh.
Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes
description In the present study, hydrolysed protein of viscera and head of Silver carp (Hypophthalmichthys molitrix) was compared using Alcalase enzyme and internal tissue enzymes at 2 and 4 hours. The result indicated that product by Alcalase (Treatment 1) had significantly higher protein and rate of hydrolysates than that produced by internal tissue enzymes (Treatment 2). So, the highest mean (±SD) protein (68.10±1.33) was related to treatment 1-head (with Alcalase enzyme) after 4 hours and the highest rate of hydrolysates (29.36±1.35) was related to treatment 1-head (with Alcalase enzyme) after 4 hours. The result indicated that rate of hydrolysates raised as time of hydrolysates increased. However the intensity and rate of hydrolysates is reduced. The highest rate of hydrolysates occurred at 120 minutes in the first. This mode was similar for two treatments. The result can be considered as the Alcalase was preferred to internal enzyme.
format Journal Contribution
topic_facet Processing
Hypophthalmichthys molitrix
Silver carp
Biotechnology
Fish
Comparison
Protein
Enzyme
Tissues
author Hosseini, Sh.
Ghoroghi, A.
Jamalzadeh, H.R.
Safari, R.
Hosseini, Sh.
author_facet Hosseini, Sh.
Ghoroghi, A.
Jamalzadeh, H.R.
Safari, R.
Hosseini, Sh.
author_sort Hosseini, Sh.
title Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes
title_short Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes
title_full Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes
title_fullStr Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes
title_full_unstemmed Comparison of produced fish protein hydrolysete from viscera and head of Silver carp (Hypophthalmichthys molitrix) using Alcalase enzyme and internal tissue enzymes
title_sort comparison of produced fish protein hydrolysete from viscera and head of silver carp (hypophthalmichthys molitrix) using alcalase enzyme and internal tissue enzymes
publishDate 2012
url http://hdl.handle.net/1834/10635
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