Characterization of alkaline protease produced by Streptomyces griseorubens E44G and its possibility for controlling Rhizoctonia root rot disease of corn

被引:23
|
作者
Al-Askar, Abdulaziz Abdulrahman [1 ]
Rashad, Younes Mohamed [2 ]
Hafez, Elsayed Elsayed [3 ]
Abdulkhair, Waleed Mohamed [4 ]
Baka, Zakaria Awad [5 ]
Ghoneem, Khalid Mohamed [6 ]
机构
[1] King Saud Univ, Fac Sci, Dept Bot & Microbiol, Riyadh, Saudi Arabia
[2] King Saud Univ, Teachers Coll, Dept Sci, Riyadh, Saudi Arabia
[3] City Sci Res & Technol Applicat, Arid Lands Cultivat Res Inst, Plant Protect & Biomol Diag Dept, Alexandria, Egypt
[4] Natl Org Drug Control & Res, Dept Microbiol, Gen Dept Basic Med Sci, Giza, Egypt
[5] Damietta Univ, Dept Bot, Coll Sci, Dumyat, Egypt
[6] Agr Res Ctr, Plant Pathol Res Inst, Dept Seed Pathol Res, Giza, Egypt
关键词
purification; characterization; antifungal; protease; EXTRACELLULAR METABOLITES; PARTIAL-PURIFICATION; ANTIFUNGAL ACTIVITY;
D O I
10.1080/13102818.2015.1015446
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The antifungal activity of Streptomyces griseorubens E44G against Rhizoctonia solani, the causal agent of root rot disease of corn, was investigated. The mycelial growth of R. solani was inhibited by S. griseorubens E44G, indicating that it has an antifungal potential. The antagonist, S. griseorubens E44G, was detected to have proteolytic activity, using the method of casein hydrolysis. Moreover, the protease production was optimized under submerged conditions. The purification and precipitation of protease were achieved by ammonium sulphate and Sephadex G-100 gel filtration chromatography. Protease activity was detected spectrophotometrically based on the production of tyrosine. The molecular weight of the enzyme (35 kDa) was determined by sodium dodecyl sulphate polyacrylamide gel electrophoresis . The optimum activity of the enzyme was detected at pH 8.5 and 60 degrees C. The results indicated that the enzyme was thermostable and retained full activity even after 1 hour of incubation at 60 degrees C. The purified enzyme substantially inhibited the growth of R. solani, indicating that this enzyme may be actually involved in the antagonistic process.
引用
收藏
页码:457 / 462
页数:6
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