Mishra Shruti, Dubey Rama Shanker
Department of Biochemistry, Faculty of Science, Banaras Hindu University, Varanasi, India.
J Plant Physiol. 2006 Sep;163(9):927-36. doi: 10.1016/j.jplph.2005.08.003. Epub 2005 Oct 3.
When seedlings of two rice (Oryza sativa L.) cvs. Malviya-36 and Pant-12 were raised under 25 and 50 microM As2O3 in the medium an increase in the level of RNA, proteins and proline accompanied with a decline in the level of free amino acid pool was observed under arsenic supplementation compared to controls. In situ As3+ treatment caused a marked inhibition in activities of ribonuclease (RNase, EC 3.1.27.1), protease and leucine aminopeptidase (LAP, EC 3.4.11.1) whereas the activity level of carboxypeptidase (EC 3.4.16.5) was enhanced. In vitro supply of As2O3 in the enzyme assay medium beyond 400 microM resulted in gradual inhibition of RNase and beyond 5 microM inhibition of LAP activities. Addition of 1M proline in the assay medium significantly restored the loss in RNase activity due to in vitro arsenic treatment or due to osmotic stress created by incorporation of polyethylene glycol (PEG). Isoform pattern of RNase extracted from As3+ -exposed seedlings showed a significant alteration compared to its pattern in unexposed seedlings. Results suggest that arsenic exposure impairs hydrolysis of RNA and proteins in rice seedlings due to inhibition of RNase and proteases activities and that proline accumulating under As3+ toxicity appears to serve as enzyme protectant.
当两个水稻(Oryza sativa L.)品种Malviya - 36和Pant - 12的幼苗在添加了25和50微摩尔三氧化二砷的培养基中培养时,与对照相比,在添加砷的情况下,观察到RNA、蛋白质和脯氨酸水平增加,同时游离氨基酸池水平下降。原位砷(As3+)处理显著抑制了核糖核酸酶(RNase,EC 3.1.27.1)、蛋白酶和亮氨酸氨肽酶(LAP,EC 3.4.11.1)的活性,而羧肽酶(EC 3.4.16.5)的活性水平则增强。在酶测定培养基中体外供应超过400微摩尔的三氧化二砷会导致核糖核酸酶逐渐受到抑制,超过5微摩尔则会抑制亮氨酸氨肽酶的活性。在测定培养基中添加1M脯氨酸可显著恢复因体外砷处理或因加入聚乙二醇(PEG)造成的渗透胁迫导致的核糖核酸酶活性损失。从暴露于砷(As3+)的幼苗中提取的核糖核酸酶同工型模式与其在未暴露幼苗中的模式相比有显著改变。结果表明,砷暴露会因抑制核糖核酸酶和蛋白酶的活性而损害水稻幼苗中RNA和蛋白质的水解,并且在砷(As3+)毒性下积累的脯氨酸似乎起到了酶保护剂的作用。