Characterisation of Endo-Polygalacturonases Activities of Rice (Oryza sativa) Fungal Pathogens in Nigeria, West Africa

A. O. Adejuwon, M. Donova, V. Tsygankova, O. Obayemi
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Abstract

Rice (Oryza sativa) is cultivated in swampy geographical locations of tropical Nigeria, West Africa. Here it is infected by a host of fungal pathogens on the field or contaminated at postharvest. This has led to its loss and reduction in its production in both the national and global market. Lasiodiplodia theobromae and Rhizoctonia solani have recently been identified as the major fungal phytopathogens causing the deterioration of this grain on the field and at postharvest and affecting its production in Nigeria leading to gross capital loss. Hence the need to determine physiological control measures for the eradication of both phytopathogens on the field and at postharvest. In this study, tropical strains of Lasiodiplodia theobromae and Rhizoctonia solani obtained from deteriorated rice (Oryza sativa) were grown in a growth nutrient medium composed of MgSo4.7H20, K2HPO4, FeSO4.7H20, potassium nitrate and pectin at 30°C. Endo-Polygalacturonase activities were produced by the fungal isolates in the growth medium within ten days. The endo-polygalacturonases from both fungi were purified by a combination of ammonium sulphate precipitation, dialysis, gel filtration (on Sephadex G-100 column) and ion-exchange chromatography (on CM-Sephadex C-50 and CM-Sephadex C-25 columns). The molecular weight of endo-polygalacturonase from the Lasiodiplodia theobromae using Sephadex G-100 was estimated as 124,000 Daltons while that of the Rhizoctonia solani was estimated as 92,000 Daltons. The purified endo-polygalcuronase from the Lasiodiplodia theobromae exhibited optimum activity at 30°C and at pH 4.5 while that from the Rhizoctonia solani exhibited optimum activity at 32°C and at pH 5.0. The purified endo-polygalacturonases from both fungi exhibited optimum activities at 0.2% pectin concentration. They were stimulated by Ca2+ but inhibited by ethlylenediamine tetracetic acid (EDTA) and 2,4-dinitrophenol. The purified endo-polygalacturonase from the Lasiodiplodia theobromae lost 80% of its activity within 20 minutes of heat at 80°C. While the purified endo-polygalacturonase from the Rhizoctonia solani lost 82% of its activity within 20 minutes of heat at 80°C. Potassium nitrate as nitrogen source in the defined growth medium with pectin as carbon source supported highest activity of endo-polygalacturonase by the Lasiodiplodia theobromae while ammonium chloride as nitrogen source in the defined growth medium with pectin as carbon source supported highest activity of endo-polygalacturonase by the Rhizoctonia solani. In conclusion, the conditions inhibiting endo-polygalacturonases from Lasiodiplodia theobromae and Rhizoctonia solani capable of degrading the pectin portion of rice (Oryza sativa) can be adapted as feasible control measures limiting the infection and contamination of rice (Oryza sativa) by these phytopathogens on the field and at postharvest. Temperature and pH extreme from 30°C and pH 4.5 will be feasible inhibitory control measures for the growth of Lasiodiplodia theobromae on rice (Oryza sativa) in Nigeria while temperature and pH extreme from 32°C and pH 5.0 will inhibit growth of Rhizoctonia solani on the grain. These physiological conditions will preserve pectin in rice (Oryza sativa) from degradation by these two fungal phytopathogens.
西非尼日利亚稻(Oryza sativa)真菌病原菌内切多半乳糖醛酸酶活性研究
水稻(Oryza sativa)种植在西非热带尼日利亚的沼泽地理位置。在这里,它在田间被许多真菌病原体感染,或者在收获后被污染。这导致其在国内和全球市场上的损失和产量减少。最近已查明可可枯裂菌和索拉根丝核菌是造成这种谷物在田间和收获后变质的主要真菌植物病原体,并影响其在尼日利亚的生产,导致总资本损失。因此,需要确定在田间和采后根除植物病原体的生理控制措施。本研究将从变质水稻(Oryza sativa)中获得的热带枯枯病菌(Lasiodiplodia theobromae)和番茄根丝核菌(Rhizoctonia solani)在由MgSo4.7H20、K2HPO4、FeSO4.7H20、硝酸钾和果胶组成的生长营养培养基中培养,温度为30℃。真菌分离物在生长培养基中10天内产生内切-聚半乳糖醛酸酶活性。通过硫酸铵沉淀、透析、凝胶过滤(在Sephadex G-100柱上)和离子交换层析(在CM-Sephadex C-50和CM-Sephadex C-25柱上)对两种真菌的内切聚半乳糖醛酸酶进行纯化。用Sephadex G-100测定了茄根丝核菌内聚半乳糖醛酸酶的分子量为12.4万道尔顿,茄根丝核菌内聚半乳糖醛酸酶的分子量为9.2万道尔顿。在30℃、pH值为4.5的条件下,从可可裂丝虫中纯化的内聚半乳糖醛酸酶具有最佳活性,而在32℃、pH值为5.0的条件下,从茄根丝胞菌中纯化的内聚半乳糖醛酸酶具有最佳活性。从两种真菌中纯化的内聚半乳糖醛酸酶在0.2%果胶浓度下表现出最佳活性。它们受到Ca2+的刺激,但受到乙二胺四乙酸(EDTA)和2,4-二硝基苯酚的抑制。在80°C高温下加热20分钟后,纯化的内聚半乳糖醛酸酶失去了80%的活性。而在80℃高温下加热20分钟后,纯化的索拉尼根丝核菌内聚半乳糖醛酸酶活性下降82%。在以果胶为碳源的生长培养基中,硝酸钾为氮源支持可可裂裂菌的内聚半乳糖醛酸酶活性最高,而在以果胶为碳源的生长培养基中,氯化铵为氮源支持番茄根丝胞菌的内聚半乳糖醛酸酶活性最高。综上所述,在田间和采后,抑制可可枯丝枯菌和茄根丝枯菌降解水稻果胶部分的内聚半乳糖醛酸酶的条件可作为限制这两种植物病原体对水稻侵染的可行控制措施。30℃和4.5℃的极端温度和pH值对尼日利亚水稻(Oryza sativa)上的可可枯丝枯病(Lasiodiplodia theobrome)生长有抑制作用,32℃和5.0的极端温度和pH值对水稻上的茄根丝枯菌(Rhizoctonia solani)生长有抑制作用。这些生理条件将使水稻中的果胶免受这两种真菌植物病原体的降解。
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