Khalil,, K. (2003). Streptomyces MUT ANTS AND PROTOPL ST REGENERATION AS TOOLS FOR BIOCONTROL OF PLi, NT PATHOGENIC FUNGI.. Journal of Plant Production, 28(5), 3479-3496. doi: 10.21608/jpp.2003.243292
K. M. A. Khalil,. "Streptomyces MUT ANTS AND PROTOPL ST REGENERATION AS TOOLS FOR BIOCONTROL OF PLi, NT PATHOGENIC FUNGI.". Journal of Plant Production, 28, 5, 2003, 3479-3496. doi: 10.21608/jpp.2003.243292
Khalil,, K. (2003). 'Streptomyces MUT ANTS AND PROTOPL ST REGENERATION AS TOOLS FOR BIOCONTROL OF PLi, NT PATHOGENIC FUNGI.', Journal of Plant Production, 28(5), pp. 3479-3496. doi: 10.21608/jpp.2003.243292
Khalil,, K. Streptomyces MUT ANTS AND PROTOPL ST REGENERATION AS TOOLS FOR BIOCONTROL OF PLi, NT PATHOGENIC FUNGI.. Journal of Plant Production, 2003; 28(5): 3479-3496. doi: 10.21608/jpp.2003.243292
Streptomyces MUT ANTS AND PROTOPL ST REGENERATION AS TOOLS FOR BIOCONTROL OF PLi, NT PATHOGENIC FUNGI.
Genetics and Cytology Department, National Research Center, Dokki, Cairo, Egypt.
Abstract
Sixteen Streptomyces cultures.l.e, four wild type strains. eleven mutanl and one regenerated protoplast isolate were tested for their abilities to inhibit one o~ more of three locat isolates of the plant pathogenic fungi, Fusarium sdsni, Rhizo Ionia solani and Sclerotium ro/fsii. which cause root rot disease. Bacillus subtitles was used to measure the antibacterial antibiotic activity of Streptomyces strains and mutants. All tested cultures were antibacterial antibiotic producers except R 1. G2 and Sir. ebus. Mutant R4 was the best antibacterial producer.
The sixteen cultures were tested for their antifungal activity against Fu arium solani. All of them inhibited F. solani growth after three days of incubation. After seven days. the antifungal activities of two-strains, Sfr. albus and Str. Gn'seovin'dis wa~ lost. Antifungal activities of eight mutants increased by increasing incubation ~eriod. Mutants R2. R4 and G4 were the higher antifungal activity mutants against F. Jolani. The best producer was R2 mutant, either after three or seven days of incubation.1
Two strains. Sir. albus and Sir. griseoviridis were inactive against Rhizoclonia 1 lani, after three and seven days of incubation. The activities of seven cultures were decreased after seven days of incubation. Mutants R2. VT and GR were the higher antifungal activity after seven days of incubation. G1 mutant was the best antir~ngal activity against Rhizoctonia solani after three days of incubation.
All tested cultures showed antifungal activities against Sclerotium olfsii.
Three cultures. R 1. Str. a/bus and Str. griseoviridis, lost their activities after even days of incubation. Three mutants G1. G2 and G3 isolated from Sir. grise us, were higher antifungal activities against R. solani. The best antifungal activity was G2 after three and seven days of incubation. Since, G2 was inactive as antibacterial anti iotic producer so in some cases, it is advantage to use such mutant as a biocontrol st ain. On the basis of the above results, S. rolfsii showed to be very sensitive to most vf the Streptomyces tested cultures. Mutant R2 proved to be the best in its antifungal activity against two out of the three tested plant pathogenic fungi. GR. which was selected after protoplast regeneration. has a remarkable antifungal activity. It was one of three higher antifungal activities against R. solani after seven days of incubation.
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