Plant and Cell Physiology, 2001, Vol. 42, No. 4 349-357
© 2001 Oxford University Press
Characterization of an Isoform of Rice Starch Branching Enzyme, RBE4, in Developing Seeds
1 Institute of Applied Biochemistry, University of Tsukuba, Tsukuba Science City, Ibaraki, 305-8572 Japan 2 Mitsui Plant Biotechnology Research Institute, TCI D-21, Sengen 2-1-6, Tsukuba Science City, Ibaraki, 305-0047 Japan 3 Institute of Agricultural and Forest Engineering, University of Tsukuba, Tsukuba Science City, Ibaraki, 305-8572 Japan 4 Carbohydrate Science Laboratory, National Food Research Institute, Ministry of Agriculture, Forestry and Fisheries, 2-1-2 Kannondai, Tsukuba Science City, Ibaraki, 305-8642 Japan
cDNA clones encoding an isoform of starch
branching enzyme, RBE4, have been identified from a developing rice seed
cDNA library, using a synthetic oligonucleotide probe corresponding to the
N-terminal amino acid sequence of RBE4. The cDNA-derived amino acid
sequence indicated that RBE4 is initially produced as a precursor protein
of 841 amino acids, including a 53-residue transit peptide at the
N-terminus. The mature form of RBE4 shared a high degree of sequence
identity (80%) with mature RBE3, and possessed an N-terminal extra
sequence, as found in RBE3. Northern blot analysis demonstrated that the
RBE4 gene is expressed in both leaves and developing seeds. The RBE4 gene
was distinguished from the RBE1 and RBE3 genes by expression at the earlier
stages of seed development. To examine enzymatic functions of RBE4,
recombinant proteins were produced in Escherichia coli cells, and
purified by two chromatographic separations. The branched
-glucans
produced by the recombinant enzymes from potato amylose revealed the
different patterns of oligosaccharide chain transfer. The peak of major
branches of the products by RBE3 or RBE4 was 6 glucose units, whereas the
peaks of major branches of the products by RBE1 were 6 and 11 glucose
units. The similar property between RBE3 and RBE4 is supported by high
similarity of the amino acid sequences between
them.
5 Corresponding author: E-mail, koumno@sakura.cc.tsukuba.ac.jp; Fax, +81-298-55-2203.
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