2017
DOI: 10.1002/jobm.201600604
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The use of newly isolated Streptomyces strain TN258 as potential biocontrol agent of potato tubers leak caused by Pythium ultimum

Abstract: An actinomycete strain designated TN258, was isolated from Tunisian Sahara soil and selected for its antagonistic activity, especially against Pythium ultimum (P. ultimum) causing potato tubers leak. Based on the results of cultural characteristic of TN258 strain, the 16S rRNA gene nucleotide sequence (1433 bp, accession n° HE600071) and the phylogenetic analysis, we propose the assignment of our new isolate bacterium as Streptomyces TN258 strain. After culture optimization, the inhibitory effect of TN258 free… Show more

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Cited by 18 publications
(8 citation statements)
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“…Many species of bacteria, especially Bacillus, are known as biological control agents that inhibit several phytopathogenic fungi due to the production of cell wall-degrading enzymes and other antifungal metabolic products[1921]. Many Bacillus strains antagonistic to fungi have been isolated from soil[10, 2224].…”
Section: Discussionmentioning
confidence: 99%
“…Many species of bacteria, especially Bacillus, are known as biological control agents that inhibit several phytopathogenic fungi due to the production of cell wall-degrading enzymes and other antifungal metabolic products[1921]. Many Bacillus strains antagonistic to fungi have been isolated from soil[10, 2224].…”
Section: Discussionmentioning
confidence: 99%
“…Plant fungal diseases are difficult to control, which makes it possible to lead to huge economic losses. Thus, strategies to ensure that plants avoid to fungal infection should be developed, especially by the development of biological control methods [ 34 ].…”
Section: Discussionmentioning
confidence: 99%
“…The inoculum of M. phaseolina and R. solani was prepared by seeding suspensions of mycelial fragments of each isolate on Potato Dextrose Agar (PDA; BioCen, Bejucal, Mayabeque, Cuba) at 28 °C for three days in darkness. In vitro dual culture assays were conducted in 9.0 cm in diameter Petri dishes with PDA [ 37 ]. To this end, a 7.0 mm in diameter mycelial plug of the pathogen was placed at one end of the plate, and another 7.0 mm in diameter mycelial plug of the actinobacterial strain was plated at 50.0 mm apart at the opposite end.…”
Section: Methodsmentioning
confidence: 99%