Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba

This study was conducted to partially purify linalool synthase from the young leaves of Michellia alba (Cempaka Putih) from the Magnoliaceae family. The technique used to determine the amount of linalool produced from enzyme activity was the combination of solid-phase microextraction (SPME) and gas...

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Main Author: Lee, Yuan Chern
Format: Thesis
Language:English
English
Published: 2006
Subjects:
Online Access:http://psasir.upm.edu.my/id/eprint/504/
http://psasir.upm.edu.my/id/eprint/504/1/600363_fbsb_2006_20_abstrak_je__dh_pdf_.pdf
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author Lee, Yuan Chern
author_facet Lee, Yuan Chern
author_sort Lee, Yuan Chern
building UPM Institutional Repository
collection Online Access
description This study was conducted to partially purify linalool synthase from the young leaves of Michellia alba (Cempaka Putih) from the Magnoliaceae family. The technique used to determine the amount of linalool produced from enzyme activity was the combination of solid-phase microextraction (SPME) and gas chromatography with flame-ionization detecter (GCFID) technique. The substrate used for this enzyme activity assay was geranylpyrophosphate (GPP). Optimal conditions such as temperature and incubation time for SPME technique were also determined. The linalool synthase exhibited a strict requirement for a divalent metal cofactor with a preference for Mg2+, Mn2+ and K+ ions. The optimal pH and temperature of the enzyme was 6.0 and 30oC respectively. The enzyme was inhibited by 1,2-Di(2-aminoethoxy)ethane-N,N,N’N’-tetra-acetic acids (EGTA). Three steps of partial purification of enzyme were carried out, including the crude extraction of young leaves, ultra centrifugation and Mono-Q anion exchange chromatography. The partially purified linalool synthase was characterized and studied for its enzyme kinetic properties. The linalool synthase has a Km of 83µM for substrate GPP. The SPME-GCFID technique was later proved to be reliable and sensitive in determination of monoterpene products.
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institution Universiti Putra Malaysia
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language English
English
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publishDate 2006
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spelling upm-5042013-05-27T06:48:48Z http://psasir.upm.edu.my/id/eprint/504/ Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba Lee, Yuan Chern This study was conducted to partially purify linalool synthase from the young leaves of Michellia alba (Cempaka Putih) from the Magnoliaceae family. The technique used to determine the amount of linalool produced from enzyme activity was the combination of solid-phase microextraction (SPME) and gas chromatography with flame-ionization detecter (GCFID) technique. The substrate used for this enzyme activity assay was geranylpyrophosphate (GPP). Optimal conditions such as temperature and incubation time for SPME technique were also determined. The linalool synthase exhibited a strict requirement for a divalent metal cofactor with a preference for Mg2+, Mn2+ and K+ ions. The optimal pH and temperature of the enzyme was 6.0 and 30oC respectively. The enzyme was inhibited by 1,2-Di(2-aminoethoxy)ethane-N,N,N’N’-tetra-acetic acids (EGTA). Three steps of partial purification of enzyme were carried out, including the crude extraction of young leaves, ultra centrifugation and Mono-Q anion exchange chromatography. The partially purified linalool synthase was characterized and studied for its enzyme kinetic properties. The linalool synthase has a Km of 83µM for substrate GPP. The SPME-GCFID technique was later proved to be reliable and sensitive in determination of monoterpene products. 2006-02 Thesis NonPeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/504/1/600363_fbsb_2006_20_abstrak_je__dh_pdf_.pdf Lee, Yuan Chern (2006) Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba. Masters thesis, Universiti Putra Malaysia. Monoterpenes - Enzyme activation English
spellingShingle Monoterpenes - Enzyme activation
Lee, Yuan Chern
Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba
title Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba
title_full Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba
title_fullStr Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba
title_full_unstemmed Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba
title_short Partial Purification and Characterization of a Monoterpene Synthase Extracted from Young Leaves of Michellia Alba
title_sort partial purification and characterization of a monoterpene synthase extracted from young leaves of michellia alba
topic Monoterpenes - Enzyme activation
url http://psasir.upm.edu.my/id/eprint/504/
http://psasir.upm.edu.my/id/eprint/504/1/600363_fbsb_2006_20_abstrak_je__dh_pdf_.pdf