S-Adenosyl-L-Methionine:L-Methionine
S-Methyltransferase from Germinating Barley1
Purification and Localization
Maria João Pimenta*,
Tsuyoshi Kaneta,
Yvan Larondelle,
Naoshi Dohmae, and
Yuji Kamiya
Plant Hormone Function, Frontier Research Program (M.J.P., T.K.,
Y.K.), and Division of Biomolecular Characterization (N.D.), The
Institute of Physical and Chemical Research (RIKEN), 2-1 Hirosawa,
Wako-shi, Saitama, 351-0198, Japan; and The
Institute of Physical and Chemical Research (RIKEN), 2-1 Hirosawa,
Wako-shi, Saitama, 351-0198, JapanUnité de Biochimie de la
Nutrition, Université Catholique de Louvain, Place
Croix-du-Sud, 2-bt 8, 1348 Belgium (M.J.P., Y.L.)
S-Adenosyl-L-methionine:L-methionine
S-methyltransferase (MMT) catalyzes the synthesis of
S-methyl-L-methionine (SMM) from L-methionine and
S-adenosyl-L-methionine. SMM content
increases during barley (Hordeum vulgare L.)
germination. Elucidating the role of this compound is important from
both a fundamental and a technological standpoint, because SMM is the
precursor of dimethylsulfide, a biogenic source of atmospheric S and an
undesired component in beer. We present a simple purification scheme
for the MMT from barley consisting of 10% to 25% polyethylene glycol
fractionation, anion-exchange chromatography on
diethylaminoethyl-Sepharose, and affinity chromatography on
adenosine-agarose. A final activity yield of 23% and a 2765-fold
purification factor were obtained. After digestion of the protein with
protease, the amino acid sequence of a major peptide was
determined and used to produce a synthetic peptide. A polyclonal
antibody was raised against this synthetic peptide conjugated to
activated keyhole limpet hemocyanin. The antibody recognized the 115-kD
denatured MMT protein and native MMT. During barley germination, both
the specific activity and the amount of MMT protein increased.
MMT-specific activity was found to be higher in the root and shoot than
in the endosperm. MMT could be localized by an immunohistochemical
approach in the shoot, scutellum, and aleurone cells but not in the
root or endosperm (including aleurone).
1
This work was supported by the Frontier Research
Program of the Japanese government. M.J.P. received a Japanese Science
and Technology fellowship.
*
Corresponding author; e-mail pimenta{at}postman.riken.go.jp; fax
81-48-462-4691.
Plant Physiol. (1998) 118: 431-438
Copyright Clearance Center: 0032-0889/98/118//08
© 1998 American Society of Plant Physiologists