Precursor of the Inactive 2S Seed Storage Protein from the Indian
Mustard Brassica juncea Is a Novel Trypsin Inhibitor
CHARACTERIZATION, POST-TRANSLATIONAL PROCESSING STUDIES, AND
TRANSGENIC EXPRESSION TO DEVELOP INSECT-RESISTANT
PLANTS*,
Surekha
Mandal,
Pallob
Kundu,
Biswajit
Roy, and
Radha K.
Mandal
From the Department of Biochemistry, Bose Institute,
Calcutta 700054, India
A number of trypsin inhibitor (TI) genes have
been used to generate insect-resistant plants. Here we report a novel
trypsin inhibitor from Indian mustard Brassica juncea
(BjTI) that is unique in being the precursor of a 2S seed storage
protein. The inhibitory activity is lost upon processing. The predicted
amino acid sequence of the precursor based on the B. juncea
2S albumin (Bj2S) gene cloned and sequenced in this laboratory
(Bj2Sc; GenBankTM accession number X65972) showed a
soybean-TI active site-like motif GPFRI at the expected processing
site. The BjTI was found to be a thermostable Kunitz type TI that
inhibits trypsin at a molar ratio of 1:1. The 20-kDa BjTI was purified
from midmature seeds and found to be processed in vitro to
9- and 4-kDa subunits upon incubation with seed extract. The Bj2Sc
sequence was expressed in Escherichia coli pET systems as
the inhibitor precursor. The radiolabeled gene product was expressed
in vitro in a coupled transcription-translation system and
showed the expected processing into subunits. Two in vitro
expressed pre-2S proteins, mutated at Gly and Asp residues, were
processed normally to mature subunits, showing thereby no absolute
requirement of Gly and Asp residues for processing. Finally, the 2S
gene was introduced into tobacco and tomato plants. Third generation
transgenics expressing BjTI at 0.28-0.83% of soluble leaf proteins
showed remarkable resistance against the tobacco cutworm,
Spodoptera litura. This novel TI can be used in
transforming seed crops for protection to their vegetative parts and
early seed stages, when insect damage is maximal; as the seeds mature,
the TI will be naturally processed to the inactive storage protein that
is safe for consumption.
*
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The on-line version of this article (available at
http://www.jbc.org) contains three additional tables and three
additional figures.
To whom correspondence should be addressed. Tel.:
91-33-351-8055; Fax: 91-33-334-3886; E-mail:
rkmandal@hotmail.com.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.