Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance
Skim latex from Hevea brasiliensis consists of many useful proteins and enzymes that can be utilized to produce value-added products for industrial purposes. In this project, to enhance the properties of the recovered lipase from skim latex serum, this enzyme was immobilized via cross-linked enzym...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Penerbit Universiti Kebangsaan Malaysia
2020
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| Online Access: | http://journalarticle.ukm.my/15709/ http://journalarticle.ukm.my/15709/1/49_01_16.pdf |
| _version_ | 1848813865456893952 |
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| author | Nur Amalin Ab Aziz Al Safi, Faridah Yusof, |
| author_facet | Nur Amalin Ab Aziz Al Safi, Faridah Yusof, |
| author_sort | Nur Amalin Ab Aziz Al Safi, |
| building | UKM Institutional Repository |
| collection | Online Access |
| description | Skim latex from Hevea brasiliensis consists of many useful proteins and enzymes that can be utilized to produce value-added
products for industrial purposes. In this project, to enhance the properties of the recovered lipase from skim latex serum, this
enzyme was immobilized via cross-linked enzyme aggregates (CLEA) technology, and supported by magnetic nanoparticles
(MNP-CLEA-lipase). MNP-CLEA-lipase was prepared by chemical cross-linking of enzyme aggregates with amino
functionalized MNP, which can easily be separated from the spent media after use by magnetic field. The performances of
the newly produced MNP-CLEA-lipase were compared with its unsupported counterpart, CLEA-lipase. The optimum
conditions for the preparation of CLEA-lipase was carried out by using 45% saturated (NH4)2SO4 and 50 mM glutaraldehyde
(GA), whereas for MNP-CLEA-lipase, it was carried out by using 70% saturated (NH4)2SO4 and 60 mM GA. The optimum
pH changes from 6 to 8 when CLEA-lipase is supported, while achieving a maximum of 69.92% residual activity (RA)
compared to 20.66% for the unsupported CLEA-lipase. However, the optimum temperature for both are the same (35°C),
with MNP-CLEA-lipase achieving 85.89% RA compared to 31.91% for the unsupported ones. Stability studies carried out
on both showed that MNP-CLEA-lipase has higher thermal (25–60°C) and pH (5–10) stabilities compared to its unsupported
counterparts. As for the reusability of enzymes, MNP-CLEA-lipase retained 56.46% of residual activity after six cycles of
reuse. The FESEM results showed that the MNP-CLEA-lipase is a Type 2, which is less structured, and this has bearings
towards its activities. FTIR analysis showed the presence of Amide I and Amide II bands in MNP-CLEA-lipase, originating
from the newly formed cross-linked between the silanized MNP and CLEA-lipase. Overall, MNP supported CLEA-lipase
showed better performance compared to the unsupported biocatalyst. |
| first_indexed | 2025-11-15T00:24:59Z |
| format | Article |
| id | oai:generic.eprints.org:15709 |
| institution | Universiti Kebangasaan Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T00:24:59Z |
| publishDate | 2020 |
| publisher | Penerbit Universiti Kebangsaan Malaysia |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | oai:generic.eprints.org:157092020-11-18T06:05:50Z http://journalarticle.ukm.my/15709/ Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance Nur Amalin Ab Aziz Al Safi, Faridah Yusof, Skim latex from Hevea brasiliensis consists of many useful proteins and enzymes that can be utilized to produce value-added products for industrial purposes. In this project, to enhance the properties of the recovered lipase from skim latex serum, this enzyme was immobilized via cross-linked enzyme aggregates (CLEA) technology, and supported by magnetic nanoparticles (MNP-CLEA-lipase). MNP-CLEA-lipase was prepared by chemical cross-linking of enzyme aggregates with amino functionalized MNP, which can easily be separated from the spent media after use by magnetic field. The performances of the newly produced MNP-CLEA-lipase were compared with its unsupported counterpart, CLEA-lipase. The optimum conditions for the preparation of CLEA-lipase was carried out by using 45% saturated (NH4)2SO4 and 50 mM glutaraldehyde (GA), whereas for MNP-CLEA-lipase, it was carried out by using 70% saturated (NH4)2SO4 and 60 mM GA. The optimum pH changes from 6 to 8 when CLEA-lipase is supported, while achieving a maximum of 69.92% residual activity (RA) compared to 20.66% for the unsupported CLEA-lipase. However, the optimum temperature for both are the same (35°C), with MNP-CLEA-lipase achieving 85.89% RA compared to 31.91% for the unsupported ones. Stability studies carried out on both showed that MNP-CLEA-lipase has higher thermal (25–60°C) and pH (5–10) stabilities compared to its unsupported counterparts. As for the reusability of enzymes, MNP-CLEA-lipase retained 56.46% of residual activity after six cycles of reuse. The FESEM results showed that the MNP-CLEA-lipase is a Type 2, which is less structured, and this has bearings towards its activities. FTIR analysis showed the presence of Amide I and Amide II bands in MNP-CLEA-lipase, originating from the newly formed cross-linked between the silanized MNP and CLEA-lipase. Overall, MNP supported CLEA-lipase showed better performance compared to the unsupported biocatalyst. Penerbit Universiti Kebangsaan Malaysia 2020 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/15709/1/49_01_16.pdf Nur Amalin Ab Aziz Al Safi, and Faridah Yusof, (2020) Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance. Malaysian Applied Biology, 49 (1). pp. 141-152. ISSN 0126-8643 http://www.mabjournal.com/index.php?option=com_content&view=article&id=981&catid=59:current-view&Itemid=56 |
| spellingShingle | Nur Amalin Ab Aziz Al Safi, Faridah Yusof, Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| title | Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| title_full | Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| title_fullStr | Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| title_full_unstemmed | Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| title_short | Immobilization of CLEA-lipase of Hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| title_sort | immobilization of clea-lipase of hevea brasiliensis onto magnetic nanoparticles for enhanced biocatalytic performance |
| url | http://journalarticle.ukm.my/15709/ http://journalarticle.ukm.my/15709/ http://journalarticle.ukm.my/15709/1/49_01_16.pdf |