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Correct Processing of the Kiwifruit Protease Actinidin in Transgenic Tobacco Requires the Presence of the C-Terminal Propeptide
Author(s) -
Wyatt Paul,
J. Amiss,
R. Try,
Uta Praekelt,
Rodney J. Scott,
H. SMITH
Publication year - 1995
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.108.1.261
Subject(s) - cauliflower mosaic virus , proteases , biology , complementary dna , protease , biochemistry , protein precursor , transgene , in vitro , microbiology and biotechnology , genetically modified crops , chemistry , gene , enzyme
A 355 cauliflower mosaic virus promoter and a tapetum-specific promoter were used to direct the synthesis in tobacco of preproactinidin and a derivative that lacked a C-terminal extension. Preproactinidin was processed into a form that migrated identically on protein gels with mature actinidin extracted from kiwifruit. This protein was proteolytically active in vitro, and high-level accumulation of this protein appeared to be detrimental to plant growth. Plants expressing an actinidin cDNA construct that lacked the sequence encoding the C-terminal propeptide were phenotypically normal but accumulated N-proactinidin, which was proteolytically active in vitro but did not self-cleave to mature actinidin. In transgenic tobacco, the C-terminal extension of actinidin is therefore required for correct processing.

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