The plant aspartic proteinase-specific polypeptide insert is not directly related to the activity of oryzasin 1

被引:28
作者
Asakura, T
Matsumoto, I
Funaki, J
Arai, S
Abe, K
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Appl Biol Chem, Bunkyo Ku, Tokyo 1138657, Japan
[2] Atomi Jr Coll, Food Sci Lab, Tokyo, Japan
[3] Fukuoka Womens Univ, Fac Environm Sci, Fukuoka, Japan
[4] Tokyo Univ Agr, Dept Nutr Sci, Tokyo, Japan
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2000年 / 267卷 / 16期
关键词
expression; Escherichia coli; aspartic proteinase; rice;
D O I
10.1046/j.1432-1327.2000.01582.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many plant aspartic proteinases (APs) are different from animal and microbial APs in that they contain a polypeptide insert, approximate to 100 amino acids in length, in the C-terminal region. To interpret the significance of this insert, we constructed an expression system for rice AP oryzasin 1 by linking a pro-oryzasin 1 downstream of glutathione S-transferase (GST). GST-proOS1 expressed the highest degree of hemoglobin-hydrolytic activity when treated at pH 3.3 and incubated for 24 h at room temperature. We carried out a similar experiment using an insert-lacking proOS1 mutant, GST-Delta proOS1, as the fusion protein, and found it to show similar activity. This result indicates that the insert is not involved in the production of AP activity. We then investigated the autolysis of the two proteins by Western blot analysis. GST-proOS1 was autolyzed into 67- and 64-kDa fragments, while GST-Delta proOS1 autolyzed to 54- and 52-kDa products. GST-Delta proOS1 clearly produced two molecular species early in the autolytic process, and not later than 3 h from the start, but no such clear result was observed in the case of GST-proOS1. This suggests that, although the presence of the plant AP-specific insert does not influence the enzyme activity by itself, it apparently has an effect on the autolysis of OS1.
引用
收藏
页码:5115 / 5122
页数:8
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