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编码一种在紫草产紫草素愈伤组织菌株中优先表达的新型质外体蛋白的cDNA的分子克隆与鉴定

Molecular cloning and characterization of a cDNA encoding a novel apoplastic protein preferentially expressed in a shikonin-producing callus strain of Lithospermum erythrorhizon.

作者信息

Yamamura Yoshimi, Sahin F Pinar, Nagatsu Akito, Mizukami Hajime

机构信息

Graduate School of Pharmaceutical Sciences, Nagoya City University, Mizuho-ku, Nagoya, 467-8603 Japan.

出版信息

Plant Cell Physiol. 2003 Apr;44(4):437-46. doi: 10.1093/pcp/pcg057.

DOI:10.1093/pcp/pcg057
PMID:12721385
Abstract

A cDNA (LEPS-2) encoding a novel cell wall protein was cloned from shikonin-producing callus tissues of Lithospermum erythrorhizon by differential display between a shikonin-producing culture strain and a non-producing strain. The LEPS-2 cDNA encoded a polypeptide of 184 amino acids. The deduced amino acid sequence exhibited no significant homology with known proteins. Expression of LEPS-2 gene as well as accumulation of LEPS-2 protein was highly correlated with shikonin production in L. erythrorhizon cells in culture. In the intact plant, expression of LEPS-2 was detected only in the roots where shikonin pigments accumulated. Cell fractionation experiments and immunocytochemical analysis showed that the protein was localized in the apoplast fraction of the cell walls. The shikonin pigments were also stored on the cell walls as oil droplets. These results indicate that expression of the LEPS-2 is closely linked with shikonin biosynthesis and the LEPS-2 protein may be involved in the intra-cell wall trapping of shikonin pigments.

摘要

通过对紫草素产生菌株和非产生菌株进行差异显示,从紫草的紫草素产生愈伤组织中克隆出一个编码新型细胞壁蛋白的cDNA(LEPS-2)。LEPS-2 cDNA编码一个由184个氨基酸组成的多肽。推导的氨基酸序列与已知蛋白质无显著同源性。LEPS-2基因的表达以及LEPS-2蛋白的积累与培养的紫草细胞中紫草素的产生高度相关。在完整植株中,仅在积累紫草素色素的根部检测到LEPS-2的表达。细胞分级分离实验和免疫细胞化学分析表明,该蛋白定位于细胞壁的质外体部分。紫草素色素也作为油滴储存在细胞壁上。这些结果表明,LEPS-2的表达与紫草素生物合成密切相关,并且LEPS-2蛋白可能参与紫草素色素在细胞壁内的捕获。

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