Involvement of α-amylase I-1 in starch degradation in rice chloroplasts

被引:108
作者
Asatsuma, S
Sawada, C
Itoh, K
Okito, M
Kitajima, A
Mitsui, T [1 ]
机构
[1] Niigata Univ, Grad Sch Sci & Technol, Labs Plant & Microbial Genome Control, Niigata 9502181, Japan
[2] Niigata Univ, Dept Appl Biol Chem, Niigata 9502181, Japan
关键词
alpha-amylase; chloroplast; glycoprotein; Golgi complex; Oryza sativa L; starch; transgenic plant;
D O I
10.1093/pcp/pci091
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
To determine the role of alpha-amylase isoform I-1 in the degradation of starch in rice leaf chloroplasts, we generated a series of transgenic rice plants with suppressed expression or overexpression of alpha-amylase I-1. In the lines with suppressed expression of alpha-amylase I-1 at both the mRNA and protein levels, seed germination and seedling growth were markedly delayed in comparison with those in the wild-type plants. However, the growth retardation was overcome by supplementation of sugars. Interestingly, a significant increase of starch accumulation in the young leaf tissues was observed under a sugar-supplemented condition. In contrast, the starch content of leaves was reduced in the plants overexpressing alpha-amylase I-1. In immunocytochemical analysis with specific anti-alpha-amylase I-1 antiserum, immuno-gold particles deposited in the chloroplasts and extracellular space in young leaf cells. We further examined the expression and targeting of alpha-amylase I-1 fused with the green fluorescent protein in re-differentiated green cells, and showed that the fluorescence of the expressed fusion protein co-localized with the chlorophyll autofluorescence in the transgenic cells. In addition, mature protein species of alpha-amylase I-1 bearing an oligosaccharide side chain were detected in the isolated chloroplasts. Based on these results, we concluded that alpha-amylase I-1 targets the chloroplasts through the endoplasmic reticulum-Golgi system and plays a significant role in the starch degradation in rice leaves.
引用
收藏
页码:858 / 869
页数:12
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