مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

76
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

11
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Antagonistic activity of cellulose-degrading bacteria isolated from soil and bovine waste against some phytopathogenic fungi

Pages

  1431-1436

Abstract

 Cellulolytic bacteria can be found in soil and ruminal wastes. The present study was conducted to isolate and identify cellulose degrading bacteria from forest soil and bovine waste and their screening for potential antifungal activity. The cellulolytic bacteria were isolated from the samples by serial dilution method on modified Czapeck (CMC) agar and following Congo red assay. Seventeen isolates were selected on the basis of cellulolytic activity through Congo red assay. The antifungal activity of these isolates was also determined against different phytopathogenic fungi including Alternaria, Cladosporium, Verticillium, Fusarium, Mucor and Rhizopus. The isolates were identified using standard biochemical tests according to Bergey’ s manual. Among the 17 isolates, 11 to Bacillus spp., 2 to Pseudomonas spp., 1 to Citrobacter spp., 3 to Staphylococcus spp. belonged. The antifungal activity against the target phytopathogens was shown by the 2 isolates of Bacillus. Isolate Bacillus spp. R7 from the bovine waste showed high activity against Alternaria by giving a zone of inhibition of 16 mm while isolate R1 from the forest soil showed antifungal activity against Fusarium by giving a clear zone of 13 mm. Based on the results of sequencing isolates R7 and R1 were most similar (more than 90% identity) to Bacillus licheniformis and Bacillus Subtilis strains, respectively. The results of the present study show that most cellulolytic bacteria isolated from soil and bovine waste belonged to the Bacillus that some of them had antifungal activity, so they are promising for biocontrol of phythopathogens and it is possible to use them as an effective strategy to manage plant diseases and protect the environment.

Multimedia

  • No record.

    • Cites

  • No record.

    • References

  • No record.

    • Cite

    APA: Copy

    Mokabber, Shaghayegh, & AHANI AZARI, ANIA. (2021). Antagonistic activity of cellulose-degrading bacteria isolated from soil and bovine waste against some phytopathogenic fungi. INTERNATIONAL JOURNAL OF MOLECULAR AND CLINICAL MICROBIOLOGY, 11(1), 1431-1436. SID. https://sid.ir/paper/973228/en

    Vancouver: Copy

    Mokabber Shaghayegh, AHANI AZARI ANIA. Antagonistic activity of cellulose-degrading bacteria isolated from soil and bovine waste against some phytopathogenic fungi. INTERNATIONAL JOURNAL OF MOLECULAR AND CLINICAL MICROBIOLOGY[Internet]. 2021;11(1):1431-1436. Available from: https://sid.ir/paper/973228/en

    IEEE: Copy

    Shaghayegh Mokabber, and ANIA AHANI AZARI, “Antagonistic activity of cellulose-degrading bacteria isolated from soil and bovine waste against some phytopathogenic fungi,” INTERNATIONAL JOURNAL OF MOLECULAR AND CLINICAL MICROBIOLOGY, vol. 11, no. 1, pp. 1431–1436, 2021, [Online]. Available: https://sid.ir/paper/973228/en

    Related Journal Papers

  • No record.

    • Related Seminar Papers

  • No record.

    • Related Plans

  • No record.

    • Recommended Workshops






    Move to top
    email sharing button
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    sharethis sharing button