Characterization of osmolyte betaine synthesizing sarcosine dimethylglycine <Emphasis Type="Italic">N</Emphasis>-methyltransferase from <Emphasis Type="Italic">Methanohalophilus portucalensis</Emphasis> |
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Authors: | Shih-Ya Chen Mei-Chin Lai Shu-Jung Lai Yu-Chien Lee |
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Institution: | (1) Department of Life Sciences, National Chung Hsing University, Taichung, 40227, Taiwan, ROC; |
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Abstract: | To overcome the extracellular salt stress, Methanohalophilus portucalensis FDF1T synthesizes the compatible solute betaine through the methylation of glycine, sarcosine, and N,N-dimethylglycine. S-adenosylmethionine (AdoMet) is the methyl donor. The enzyme sarcosine dimethylglycine N-methyltransferase (SDMT) of M. portucalensis, that catalyzes the formation of N,N-dimethylglycine and glycine betaine, has been purified and characterized. SDMT, a monomer of 33 kDa with a pI at 5.03, has
a narrow substrate specificity limited to using only sarcosine and dimethylglycine as substrates for the methyl transferase
reaction. The K
m values for sarcosine and AdoMet were 2.29 and 0.21 mM, respectively, with a V
max of 0.83 μmol/mg-min (k
cat value of 0.44 s−1). The K
m values for dimethylglycine and AdoMet were 3.76 and 0.59 mM, respectively, with a V
max of 4.88 μmol/mg-min (k
cat of 2.68 s−1). A high concentration of the end product betaine (2.0 M) did not affect the SMT activity, but it slightly inhibited the
DMT activity. Both activities were also not affected by potassium or sodium ions in concentrations of 200–1,000 mM. We compared
this novel archaeal SDMT enzyme to other similar bacterial transferases as well as to the glycine sarcosine dimethylglycine
methyltransferase found also in M. portucalensis. |
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Keywords: | |
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