Characterization of a plant S-adenosylmethionine synthetase from Acacia koa

Copyright © 2024 The Author(s). Published by Elsevier Masson SAS.. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant physiology and biochemistry : PPB. - 1991. - 210(2024) vom: 09. Mai, Seite 108618
1. Verfasser: Carrillo, James T (VerfasserIn)
Weitere Verfasser: Borthakur, Dulal
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Plant physiology and biochemistry : PPB
Schlagworte:Journal Article Feedback inhibition Heterologous expression Hybrid enzyme Non-aqueous activity assay Recombinant enzyme Methionine Adenosyltransferase EC 2.5.1.6 Plant Proteins S-Adenosylmethionine 7LP2MPO46S
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520 |a The Acacia koa S-adenosylmethionine (SAM) synthetase was identified from transcriptome data and cloned into the T7-expression vector pEt14b. Assays indicate a thermoalkaliphic enzyme which tolerates conditions up to pH 10.5, 55 °C and 3 M KCl. In vitro examples of plant SAM-synthetase activity are scarce, however this study provides supporting evidence that these extremophilic properties may actually be typical for this plant enzyme. Enzyme kinetic constants (Km = 1.44 mM, Kcat = 1.29 s-1, Vmax 170 μM. min-1) are comparable to nonplant SAM-synthetases except that substrate inhibition was not apparent at 10 mM ATP/L-methionine. Methods were explored in this study to reduce feedback inhibition, which is known to limit SAM-synthetase activity in vitro. Four single-point mutation variants of the Acacia koa SAM-synthetase were produced, each with varying degrees of reduced reaction rate, greater sensitivity to product inhibition and loss of thermophilic properties. Although an enhanced mutant was not produced, this study describes the first mutagenesis of a plant SAM-synthetase. Overcoming feedback inhibition was accomplished by the addition of organic solvent to enzyme assays. Acetonitrile, methanol or dimethylformamide, when included as 25% of the assay volume, improved total SAM production by 30-65% 
650 4 |a Journal Article 
650 4 |a Feedback inhibition 
650 4 |a Heterologous expression 
650 4 |a Hybrid enzyme 
650 4 |a Non-aqueous activity assay 
650 4 |a Recombinant enzyme 
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650 7 |a EC 2.5.1.6  |2 NLM 
650 7 |a Plant Proteins  |2 NLM 
650 7 |a S-Adenosylmethionine  |2 NLM 
650 7 |a 7LP2MPO46S  |2 NLM 
700 1 |a Borthakur, Dulal  |e verfasserin  |4 aut 
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