Flow rate dependent continuous hydrolysis of protein isolates

Abstract Food protein hydrolysates are often produced in unspecific industrial batch processes. The hydrolysates composition underlies process-related fluctuations and therefore the obtained peptide fingerprint and bioactive properties may vary. To overcome this obstacle and enable the production of...

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Main Authors: Tim Sewczyk, Marieke Hoog Antink, Michael Maas, Stephen Kroll, Sascha Beutel
Format: Article
Language:English
Published: SpringerOpen 2018-02-01
Series:AMB Express
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13568-018-0548-9
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spelling doaj-a5cb6cf2f4f749b197e631e460ef723b2020-11-24T23:21:41ZengSpringerOpenAMB Express2191-08552018-02-01811910.1186/s13568-018-0548-9Flow rate dependent continuous hydrolysis of protein isolatesTim Sewczyk0Marieke Hoog Antink1Michael Maas2Stephen Kroll3Sascha Beutel4Institute for Technical Chemistry, Leibniz University HannoverAdvanced Ceramics, University BremenAdvanced Ceramics, University BremenInstitute for Bioplastics and Biocomposites, Hochschule HannoverInstitute for Technical Chemistry, Leibniz University HannoverAbstract Food protein hydrolysates are often produced in unspecific industrial batch processes. The hydrolysates composition underlies process-related fluctuations and therefore the obtained peptide fingerprint and bioactive properties may vary. To overcome this obstacle and enable the production of specific hydrolysates with selected peptides, a ceramic capillary system was developed and characterized for the continuous production of a consistent peptide composition. Therefore, the protease Alcalase was immobilized on the surface of aminosilane modified yttria stabilized zirconia capillaries with a pore size of 1.5 µm. The loading capacity was 0.3 µg enzyme per mg of capillary with a residual enzyme activity of 43%. The enzyme specific peptide fingerprint produced with this proteolytic capillary reactor system correlated with the degree of hydrolysis, which can be controlled over the residence time by adjusting the flow rate. Common food proteins like casein, sunflower and lupin protein isolates were tested for continuous hydrolysis in the developed reactor system. The peptide formation was investigated by high-performance liquid chromatography. Various trends were found for the occurrence of specific peptides. Some are just intermediately occurring, while others cumulate by time. Thus, the developed continuous reactor system enables the production of specific peptides with desired bioactive properties.http://link.springer.com/article/10.1186/s13568-018-0548-9ImmobilizationProteasesBioactive peptidesContinuous processFood protein
collection DOAJ
language English
format Article
sources DOAJ
author Tim Sewczyk
Marieke Hoog Antink
Michael Maas
Stephen Kroll
Sascha Beutel
spellingShingle Tim Sewczyk
Marieke Hoog Antink
Michael Maas
Stephen Kroll
Sascha Beutel
Flow rate dependent continuous hydrolysis of protein isolates
AMB Express
Immobilization
Proteases
Bioactive peptides
Continuous process
Food protein
author_facet Tim Sewczyk
Marieke Hoog Antink
Michael Maas
Stephen Kroll
Sascha Beutel
author_sort Tim Sewczyk
title Flow rate dependent continuous hydrolysis of protein isolates
title_short Flow rate dependent continuous hydrolysis of protein isolates
title_full Flow rate dependent continuous hydrolysis of protein isolates
title_fullStr Flow rate dependent continuous hydrolysis of protein isolates
title_full_unstemmed Flow rate dependent continuous hydrolysis of protein isolates
title_sort flow rate dependent continuous hydrolysis of protein isolates
publisher SpringerOpen
series AMB Express
issn 2191-0855
publishDate 2018-02-01
description Abstract Food protein hydrolysates are often produced in unspecific industrial batch processes. The hydrolysates composition underlies process-related fluctuations and therefore the obtained peptide fingerprint and bioactive properties may vary. To overcome this obstacle and enable the production of specific hydrolysates with selected peptides, a ceramic capillary system was developed and characterized for the continuous production of a consistent peptide composition. Therefore, the protease Alcalase was immobilized on the surface of aminosilane modified yttria stabilized zirconia capillaries with a pore size of 1.5 µm. The loading capacity was 0.3 µg enzyme per mg of capillary with a residual enzyme activity of 43%. The enzyme specific peptide fingerprint produced with this proteolytic capillary reactor system correlated with the degree of hydrolysis, which can be controlled over the residence time by adjusting the flow rate. Common food proteins like casein, sunflower and lupin protein isolates were tested for continuous hydrolysis in the developed reactor system. The peptide formation was investigated by high-performance liquid chromatography. Various trends were found for the occurrence of specific peptides. Some are just intermediately occurring, while others cumulate by time. Thus, the developed continuous reactor system enables the production of specific peptides with desired bioactive properties.
topic Immobilization
Proteases
Bioactive peptides
Continuous process
Food protein
url http://link.springer.com/article/10.1186/s13568-018-0548-9
work_keys_str_mv AT timsewczyk flowratedependentcontinuoushydrolysisofproteinisolates
AT mariekehoogantink flowratedependentcontinuoushydrolysisofproteinisolates
AT michaelmaas flowratedependentcontinuoushydrolysisofproteinisolates
AT stephenkroll flowratedependentcontinuoushydrolysisofproteinisolates
AT saschabeutel flowratedependentcontinuoushydrolysisofproteinisolates
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