TISSUE DISTRIBUTION AND BIOCHEMICAL CHARACTERIZATION OF BETA-CYANOALANINE SYNTHASE FROM COMMON BEAN SEEDS (PHASEOLUS VULGARIS)

EN Ezima, A. Ademakinwa, Temitope Fasanya, A. A. Adelegan, A. E. Ojo
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Abstract

Cyanide is produced throughout a plant's life cycle, its production increases during certain developmental stages such as seed germination, seedling elongation, fruit ripening and senescence. Beta-cyanoalanine synthase is the most important cyanide metabolizing enzyme found in plants. This work is aimed at studying the tissue distribution, partial purification and some physicochemical properties of β-cyanoalanine synthase from bean seeds (Phaseolus vulgaris). β-cyanolalanine synthase was isolated and partially purified using a combination of ammonium sulphate precipitation, desalting on Sephadex G-10 and gel filtration chromatography on Sephacryl S-200 column. The biochemical characteristics of the enzyme were investigated. Results obtained from this work showed that β-cyanolalanine synthase is more concentrated in the seeds (20.53 nmol/HS/mg) when compared 2 to the cotyledons (10.08 nmol/HS/mg) and the seed coats (5.82 nmol/HS/mg). The partially purified 2 2 enzyme showed a specific activity of 26.77 nmol/HS/mg and an apparent molecular weight of about 2 60,000Da, K values for cyanide and L-cysteine of  0.741 mM and 1.724 mM respectively. The V max m value obtained for cyanide was 25.00 nmol/H S/ml/minwhile that of L-cysteine was 2 o666.67nmol/H S/ml/min. The enzyme showed an optimum temperature of 40C and optimum pH of 2 10.0.Studies on the effect of chloride salt indicated that NaCl and MnCl had strong inhibitory effect 2 on the enzyme; NHCl had slight negative effect while KCl and ZnCl activated the enzyme dose 4 2 dependently.This study showed the presence of β-cyanoalanine synthase in bean seeds which is believed to function in the detoxification of cyanide produced in its tissues especially during germination.
菜豆种子β -氰丙氨酸合成酶的组织分布及生化特性
氰化物在植物的整个生命周期中产生,在种子萌发、幼苗伸长、果实成熟和衰老等某些发育阶段,氰化物的产生会增加。-氰丙氨酸合成酶是植物中发现的最重要的氰化物代谢酶。本研究旨在研究蚕豆种子中β-氰丙氨酸合成酶的组织分布、部分纯化及其部分理化性质。采用硫酸铵沉淀、Sephadex G-10脱盐和sepphacryl S-200凝胶过滤层析相结合的方法分离和部分纯化了β-三聚丙氨酸合成酶。研究了该酶的生化特性。结果表明,β-三聚丙氨酸合成酶在种子中的含量(20.53 nmol/HS/mg)高于子叶(10.08 nmol/HS/mg)和种皮(5.82 nmol/HS/mg)。部分纯化的22酶比活性为26.77 nmol/HS/mg,表观分子量约为26万da,对氰化物和l -半胱氨酸的K值分别为0.741 mM和1.724 mM。氰化物的vmax m值为25.00 nmol/H S/ml/min, l -半胱氨酸的vmax m值为2 o666.67nmol/H S/ml/min。该酶的最适温度为40℃,最适pH为2.10.0。对氯盐作用的研究表明,NaCl和MnCl对该酶有较强的抑制作用;NHCl对酶有轻微的负作用,KCl和ZnCl对酶的激活剂量为4.2。本研究表明,大豆种子中存在β-氰丙氨酸合成酶,该酶被认为在其组织中产生的氰化物解毒中起作用,特别是在萌发过程中。
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