Senyuk V, Rotari V, Becker C, Zakharov A, Horstmann C, Müntz K, Vaintraub I
Laboratory of Protein Chemistry, State University of Moldova, Kishinev, Republic Moldova.
Eur J Biochem. 1998 Dec 1;258(2):546-58. doi: 10.1046/j.1432-1327.1998.2580546.x.
An asparaginyl-specific cysteine endopeptidase which was named 'legumain-like proteinase' (LLP) and has an apparent molecular mass of 38.1 kDa was isolated from cotyledons of kidney bean (Phaseolus vulgaris L.) seedlings and partially characterized. It is, to our knowledge, the first known proteinase which in vitro extensively degrades native phaseolin, the major storage globulin of this grain legume. Phaseolin that in vitro had been partially degraded by LLP (Pvitro) and phaseolin that was isolated after partial in vivo breakdown 6 days after the start of seed imbibition (Pvivo) showed similar fragment patterns on SDS/polyacrylamide gels. The fragments had identical cleavage sites in Pvitro and Pvivo as determined by partial amino acid sequencing. In both types of partially degraded phaseolin, these cleavage sites have asparagine in the P1 position. Two of the cleavage sites are located in the beta-barrel domain of the C-terminal module and only one cleavage site was found in the beta-barrel domain of the N-terminal module according to the consensus structural model of phaseolin subunits. These results suggest that very likely LLP could in vivo be responsible for the initiation of phaseolin proteolysis. Two different legumain-specific clones named cp6b and p21b were isolated from a cDNA library of germinated bean cotyledons. Cp6b encodes LLP, while p21b encodes a VPE-like enzyme. Southern-blot analysis revealed a single gene copy for Pv-VPE and, presumably, at least two gene copies for LLP in the kidney bean genome. Northern-blot analysis indicated that mRNAs for both clones appear de novo during seed germination. However, the developmental patterns of the transcript levels corresponding to the two clones differed significantly. The temporal pattern of phaseolin degradation and of LLP polypeptide levels agreed well with the suggestion that LLP plays a key role in the mobilization of phaseolin during and after kidney bean germination.
从菜豆(Phaseolus vulgaris L.)幼苗子叶中分离出一种天冬酰胺特异性半胱氨酸内肽酶,命名为“豆球蛋白样蛋白酶”(LLP),其表观分子量为38.1 kDa,并对其进行了部分特性鉴定。据我们所知,它是以一种已知的蛋白酶,能够在体外大量降解该豆科作物主要储存球蛋白——天然菜豆蛋白。体外经LLP部分降解的菜豆蛋白(Pvitro)和种子吸胀6天后体内部分降解后分离得到的菜豆蛋白(Pvivo)在SDS/聚丙烯酰胺凝胶上显示出相似的片段模式。通过部分氨基酸测序确定,Pvitro和Pvivo中的片段具有相同的切割位点。在两种类型的部分降解菜豆蛋白中,这些切割位点的P1位置均为天冬酰胺。根据菜豆蛋白亚基的共有结构模型,其中两个切割位点位于C端模块的β桶结构域,而在N端模块的β桶结构域中仅发现一个切割位点。这些结果表明,LLP很可能在体内负责菜豆蛋白水解的起始过程。从发芽菜豆子叶的cDNA文库中分离出两个不同的豆球蛋白特异性克隆,分别命名为cp6b和p21b。Cp6b编码LLP,而p21b编码一种VPE样酶。Southern杂交分析显示,菜豆基因组中Pv-VPE有一个基因拷贝,LLP可能至少有两个基因拷贝。Northern杂交分析表明,两个克隆的mRNA在种子萌发过程中从头出现。然而,对应于两个克隆的转录水平的发育模式有显著差异。菜豆蛋白降解的时间模式和LLP多肽水平与LLP在菜豆萌发期间及之后菜豆蛋白动员中起关键作用的观点非常吻合。