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Isolation of cysteine biosynthetic cDNA and characterization of cy-o-acetylserine (thiol) lyase from Leucaena leucocephala

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dc.contributor.authorYafuso, Jannai Tetsuko
dc.date.accessioned2016-05-02T23:10:27Z-
dc.date.available2016-05-02T23:10:27Z-
dc.date.issued2013-12
dc.identifier.urihttp://hdl.handle.net/10125/100770-
dc.descriptionM.S. University of Hawaii at Manoa 2013.
dc.descriptionIncludes bibliographical references.
dc.description.abstractIn plants, the final two steps of cysteine formation are catalyzed by O-acetylserine (thiol) lyase (OAS-TL) and serine acetyltransferase (SAT). The purpose of this study was to isolate and characterize an OAS-TL from the tree-legume Leucaena leucocephala (leucaena). Leucaena contains a toxic, nonprotein amino acid, mimosine, which is also formed by an OAS-TL, and characterization of this enzyme is essential for developing a mimosine-free leucaena for its use as a protein-rich fodder. The cDNA for a putative chloroplastic OAS-TL and cytosolic SAT were isolated through Reverse Transcriptase-PCR using degenerate primers. An additional cDNA for a cytosolic leucaena OAS-TL (cy-OAS-TL) isoform was previously obtained through interspecies suppression subtractive hybridization and was selected for further characterization. SAT and cy-OAS-TL were successfully over-expressed and purified from Escherichia coli. A 40-kDa recombinant cy-OAS-TL was further studied through enzyme activity assays where it was found to synthesize only cysteine. The enzyme followed Michaelis-Menten kinetics, and the Km was calculated to be 1.850 ± 0.4146 mM sulfide and the Vmax was 200.6 ± 19.92 μM cysteine min-1. The N-terminal affinity His-tag was cleaved from the recombinant OAS-TL to eliminate its possible interference in binding with the substrate 3-hydroxy-4-pyridone for mimosine formation. The His-tag-cleaved cy-OAS-TL was again observed to catalyze the formation of cysteine but not mimosine. Thus, the cytosolic OAS-TL from leucaena used in this study is specific for only cysteine synthesis and is different from previously reported OAS-TLs that also function as β-substituted alanine synthases.
dc.language.isoeng
dc.publisher[Honolulu] : [University of Hawaii at Manoa], [December 2013]
dc.relationTheses for the degree of Master of Science (University of Hawaii at Manoa). Molecular Biosciences and Bioengineering.
dc.subjectcysteine formation
dc.subjectOAS-TL
dc.titleIsolation of cysteine biosynthetic cDNA and characterization of cy-o-acetylserine (thiol) lyase from Leucaena leucocephala
dc.typeThesis
dc.type.dcmiText
Appears in Collections:M.S. - Molecular Biosciences and Bioengineering



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