Biosynthetic genes are responsible for antibiotic production by rhizobacterial antagonists. Detection of antibiotic biosynthetic genes of an antagonist is therefore important for the identification of genes and antibiotics responsible for disease suppression. The study was carried out to detect the antibiotic producing genes of eight rhizobacteria responsible for fungal disease suppression. Eight yam (Dioscorea sp.) rhizobacterial isolates which were found to possess antifungal properties against several plant pathogenic fungi and identified as Bacillus species were tested for the presence of genes for biosynthesis of antifungal lipopeptides; bacillomycin D, iturin A, surfactin, fengycin, and aminopolyols, zwettemycin A as possible antibiotic tools for biocontrol using specific primers. The detection of bacillomycin D gene by PCR amplification, gene sequencing, and BLAST analysis, was achieved through the use of the primer pair, BACC1-F/BACC1-R, capable of detecting 875-bp region, iturin A through the use of ITUD1-F/ITUD1-R primer pair, capable of detecting 647-bp region while primer pair SUR3-F/SUR3-R, capable of detecting 441-bp region was also used for the detection of surfactin. Three separate primer pairs were used for fengycin viz. FEND1-F/FEND1-R, FENA1-F/FENA1-R, and FENB2-F/FENB2-R, capable of detecting 964-bp region corresponding to fengycin D, fengycin A and fengycin B respectively. Zwettermycin A was detected through the use of ZWET-F2/ZWET-R1 primer pair, capable of detecting 1-kb region. The outcome of the study shows that all the eight rhizobacteria possessed biosynthetic genes for the production of bacillomycin D, iturin A, and surfactin, however, neither the three types of fengycin nor the zwettermycin A were detected. Sequenced data of these antibiotics have been deposited with GenBank and the following accession numbers assigned to bacillomycin D (MW263002-MW263009), iturin A (MW263010-MW263017), and surfactin (MW263018-MW263025). All the eight rhizobacteria tested were found to possess three out of the five biosynthetic genes namely bacillomycin D, iturin A and surfactin. The detection of these biosynthetic genes confirms and justify why these rhizobacteria are potential biocontrol agents of plant pathogens.
Published in | Plant (Volume 11, Issue 4) |
DOI | 10.11648/j.plant.20231104.12 |
Page(s) | 122-129 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2023. Published by Science Publishing Group |
Antifungal, Lipidopeptides, Iturin A, Bacillomycin D, Surfactin, Fengycin and Zwettermycin A
[1] | de Vrije, T., Antoine, N., Buitelaar, R. M., Bruckner, S., Dissevelt, M., Durand, A., Gerlagh, M. and Jones, E. E. et al. The fungal biocontrol agent Coniothyrium minitans: production by solid-state fermentation, application and marketing. Applied Microbiology and Biotechnology, 2001, 56, 58–68. |
[2] | Raaijmakers, J. M., Vlami, M. and de Souza, J. T. Antibiotic production by bacterial biocontrol agents. Antonie van Leeuwenkoek, 2002, 81: 537-547. |
[3] | Köhl, J., Kolnaar, R., and Ravensberg, W. J. Mode of actions of microbial biological control agents against plant disease: Relevance beyond efficacy. Frontier in Plant Science, 2019, 10: 845. |
[4] | Kim, P. I., Bai, H., Bai, D., Chae, H., Chung, S., Kim, Y., Park, R. and Chi, Y. T. Purification and characterization of a lipopeptide produced by Bacillus thuringiensis CMB26. Journal of Applied Microbiology, 2004, 97: 942-949. |
[5] | Handelsman, J. and Stabb, E. V. Biocontrol of soil-borne plant pathogens. The Plant Cell, 1996, 8: 1855-1869. |
[6] | Yu, G. Y., Sinclair, J. B., Hartman, G. L. and Bertagnolli, B. L. Production of iturin A by Bacillus amyloliquefaciens suppressing Rhizoctonia solani. Soil Biology and Biochemistry, 2002, 34: 955–63. |
[7] | Milner, J. L. Silo-Suh, L. Lee, J. C. He, H. Clardy, J. and Handelsman, J. Production of kanosamine by Bacillus cereus UW85. Applied Environmental Microbiology, 1996, 62: 3061-3065. |
[8] | Mckeen, C. D., Relly, C. C. and Pusey, P. L. Production and partial characterization of antifungal substances antagonistic to Monilinia fructicola from Bacillus subtilis. Phytopathology, 1996, 76: 136-139. |
[9] | Cesa-Luna, C., Baez, A., Quintero-Hernández, V., De la Cruz-Enríquez, J., Castañeda- Antonio. M. D. and Muñoz-Rojas, J. The importance of antimicrobial compounds produced by beneficial bacteria on the biocontrol of phytopathogens. Acta Biologica Colombiana, 2020, 25 (1): 140-154. |
[10] | de Souza, J. T. and Raaijmakers, J. M. Polymorphisms within the prnD and the pltC genes from pyrrolnitrin and pyoluteorin-producing Pseudomonas and Burkholderia spp. FEMS Microbiology and Ecology, 2003, 43: 21-34. |
[11] | Larbi-Koranteng, S., Awuah, R. T. and Kankam, F. Biological control of black pod disease of cocoa (Theobroma cacao L.) with Bacillus amyloliquefaciens, Aspergillus sp. and Penicillium sp. in vitro and in the field. Journal of Microbiology and Antimicrobiology, 2020, 12 (2), 52-63. |
[12] | Akrasi, K. O. Anti-microbial properties of yam rhizosphere microorganisms and their potential use for controlling yam tuber rot. MSc. Thesis. Faculty of Agriculture, KNUST, Kumasi. Ghana, 2005, Pp. 104. |
[13] | Ramarathnam, R., Bo, S., Chen, Y., Fernando, W. G. D., Xuewen, G. and de Kievit, T. Molecular and biochemical detection of fengycin and bacillomycin D-producing Bacillus spp., antagonistic to fungal pathogens of canola and wheat. Canadian Journal of Microbiolology, 2007, 53 (7): 901-911. |
[14] | Altschui, S. F., Gish, W., Miller, W., Myers, E. W. and Lipman, D. J. Basic Local Alignment Search Tool. Journal of Molecular Biology, 1990, 215: 403-410. |
[15] | Moyne, A. L., Shelby, R., Cleveland, T. E. and Tuzun, S. Bacillomycin D: an iturin with antifungal activity against Aspergillus flavus. J of Appl Microbiol 90: 622–629. |
[16] | Paulitz, T. C. and Belanger, R. R. Biological control in greenhouse systems. Annual Review of Phytopathology, 2001, 39: 103-133. |
[17] | Kloepper, J. W, Ryu, C. M. and Zhang, S. Induced systemic resistance and promotion of plant growth by Bacillus spp. Phytopathology, 2004, 94: 1259-1266. |
[18] | Koumoutsi, A., Chen, X. H., Henne, A., Liesegang, H., Gabriele, H., Franke, P., Vater, J. and Borris, R. Structural and functional characterization of gene clusters directing nonribosomal synthesis of bioactive lipopeptides in Bacillus amyloliquefaciens strain FZB42. Journal of Bacteriology, 2004, 186: 1084-1096. |
[19] | Athukorala, S. N. P., Fernando, W. G. D. and Rashid, K. Y. (2009) Identification of antifungal antibiotics of Bacillus species isolated from different microhabitats using polymerase chain reaction and MALDI-TOF mass spectrometry. Canadian Journal of Microbiology, 2009, 55: 1021-1032. |
[20] | Korenbien, E., Vieira de Araujo, L., Guimarães, C. R., de Souza, L. M., Sassaki, G., Abreu, F, Nitschke, M., Lins, U., Freire, D. M. G., Barreto-Bergter, E. and Seldin, L. Purification and characterization of a surfactin-like molecule produced by Bacillus sp. H2O-1 and its antagonistic effect against sulfate reducing bacteria. BMC Microbiology, 2012, 12: 252. |
[21] | Phae, C. G., Shoda, M. and Kubota, H. Suppressive effect of Bacillus subtilis and its products on phytopathogenic microorganisms. Journal of Fermentation and Bioengineering, 1990, 69: 1–7. |
[22] | Akrasi, K. O. and Awuah, R. T. Tuber rot of yam in Ghana and evaluation of some rhizosphere bacteria for fungitoxicity to yam rot fungi. International Journal of AgriScience, 2012, 2 (7): 571-582. |
[23] | Hiroaka, H., Asaka, O., Ano, T. and Shoda, M. Characterization of Bacillus subtilis RB14, coproducer of peptide antibiotics iturin A and surfactin. Journal of General and Applied Microbiology, 1992, 38 (6): 635-640. |
[24] | Asaka, O. and Shoda, M. Biocontrol of Rhizoctonia solani damping-off of tomato with Bacillus subtilis RB14. Applied Environmental Microbiology, 1996, 62: 4081–4085. |
[25] | Ji, S. H., Cahandra, N. P., Den, J. X., Kim, Y. S., Yun, B. S. and Yu, S. H. Biocontrol activity of B. amyloliquefaciens CNU114001 against fungal plant diseases. Mycobiology, 2013 41 (4): 234-242. |
[26] | Shoda, M. Bacterial control of plant diseases. Journal of Bioscience and Bioengineering, 2000, 89: 515-21. |
[27] | Chen, X. H., Koumoutsi, A., Scholz, R., Schneider, K., Vater, J., Sussmuth, R., Piel, J. and Borriss, R. Genome analysis of Bacillus amyloliquefaciens FZB42 reveals its potential for biocontrol of plant pathogens. Journal of Biotechnology, 2009, 140, 27–37. |
[28] | Raupach, G. S. and Kloepper, J. W. Mixtures of plant growth promoting rhizobacteria enhance biological control of multiple Cucumber pathogens. Phytopathology, 1998. 88: 1158-1164. |
[29] | Koranteng, S. L. and Awuah, R. T. Biological suppression of black pod lesion development on detached cocoa pods. African Journal of Agricultural Research, 2011, 6 (1): 67-72. |
[30] | Ko, K. S., Kim, J. W., Kim, J. M., Kim, W., Chung, S. I., Kim, I. J. and Kook, Y. H. Population structure of the Bacillus cereus group as determined by sequence analysis of six housekeeping genes and the plcR gene. Infection Immunology, 2004, 72: 5253–5261. |
[31] | Koumoutsi, A. Functional genome analysis of the plant-growth promoting bacterium Bacillus amyloliquefaciens strain FZB42; characterizing its production and regulation of nonribosomal peptide synthetases. PhD Dissertation, Humboldt-Universitat, Berlin, 2006. |
[32] | Hou, X., Boyetchko, S. M., Brkic, M., Olson, D., Ross, A. and Hegedus, D. Characterization of the anti-fungal activity of a Bacillus spp. associated with sclerotia from Sclerotinia sclerotiorum. Applied Microbiology and Biotechnology, 2006, 72: 644–653. |
[33] | Arguelles-Arias, A., Ongena, M., Halimi, B., Lara, Y., Brans, A., Joris, B. and Fickers, P. Bacillus amyloliquefaciens GA1 as a source of potent antibiotics and other secondary metabolites for biocontrol of plant pathogens. Microbial Cell Fact, 2009, 8: 63–70. |
[34] | Ongena, M., Adam, A., Jourdan, E., Paquot, M., Brans, A., Joris, B., Arpigny, J. L. and Thonart, P. Surfactin and fengycin lipopeptides of Bacillus subtilis as elicitors of induced systemic resistance in plants. Environmental Microbiology, 2007, 9: 1084-1090. |
[35] | Romero, D., Vicente, A., Rakotoaly, R., Dufour, S., Veening, J. and Arrebola, E. The iturin and fengycin families of lipopeptides are key factors in antagonism of Bacillus subtilis toward Podosphaera fusca. Molecular Plant Microbe Interaction, 2007, 20: 430-440. |
[36] | Zeriouh, H., Romero, D., Garcia-Gutierrez, L., Cazorla, F. M., de Vicente, A., Perez-Garcia, A. (2011). The iturin-like lipopeptides are essential components in the biological control arsenal of Bacillus subtilis against bacterial diseases of cucurbits. Molecular Plant-Microbe Interaction, 2011, 24: 1540–1552. |
[37] | Zeriouh, H., de Vicente, A., Perez-Garcia, A., Romero, D. Surfactin triggers biofilm formation of Bacillus subtilis in melon phylloplane and contributes to the biocontrol activity. Environmental Microbiology, 2014, 16: 2196–2211. |
[38] | Ramarathnam, R. Phyllosphere bacterial biological control of Leptosphaeria maculans, the blackleg pathogen of canola (Brassica napus L.): screening for potential antibiotic producers, investigation of the mechanism of control, biochemical detection of the antifungal compounds, and establishment of the role of antibiosis. Ph.D. thesis, University of Manitoba, Winnipeg, Manitoba, 2007. |
APA Style
Stephen, L., Richard, A. T., Dorcas, Q. M., Frederick, K., Abdulai, M., et al. (2023). Molecular Detection of Biosynthetic Genes for Anti-fungal Metabolite Production by Yam (Dioscorea sp.) Rhizobacteria. Plant, 11(4), 122-129. https://doi.org/10.11648/j.plant.20231104.12
ACS Style
Stephen, L.; Richard, A. T.; Dorcas, Q. M.; Frederick, K.; Abdulai, M., et al. Molecular Detection of Biosynthetic Genes for Anti-fungal Metabolite Production by Yam (Dioscorea sp.) Rhizobacteria. Plant. 2023, 11(4), 122-129. doi: 10.11648/j.plant.20231104.12
@article{10.11648/j.plant.20231104.12, author = {Larbi-Koranteng Stephen and Awuah Tuyee Richard and Quain Marian Dorcas and Kankam Frederick and Muntala Abdulai and Yükselbaba Utku}, title = {Molecular Detection of Biosynthetic Genes for Anti-fungal Metabolite Production by Yam (Dioscorea sp.) Rhizobacteria}, journal = {Plant}, volume = {11}, number = {4}, pages = {122-129}, doi = {10.11648/j.plant.20231104.12}, url = {https://doi.org/10.11648/j.plant.20231104.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.plant.20231104.12}, abstract = {Biosynthetic genes are responsible for antibiotic production by rhizobacterial antagonists. Detection of antibiotic biosynthetic genes of an antagonist is therefore important for the identification of genes and antibiotics responsible for disease suppression. The study was carried out to detect the antibiotic producing genes of eight rhizobacteria responsible for fungal disease suppression. Eight yam (Dioscorea sp.) rhizobacterial isolates which were found to possess antifungal properties against several plant pathogenic fungi and identified as Bacillus species were tested for the presence of genes for biosynthesis of antifungal lipopeptides; bacillomycin D, iturin A, surfactin, fengycin, and aminopolyols, zwettemycin A as possible antibiotic tools for biocontrol using specific primers. The detection of bacillomycin D gene by PCR amplification, gene sequencing, and BLAST analysis, was achieved through the use of the primer pair, BACC1-F/BACC1-R, capable of detecting 875-bp region, iturin A through the use of ITUD1-F/ITUD1-R primer pair, capable of detecting 647-bp region while primer pair SUR3-F/SUR3-R, capable of detecting 441-bp region was also used for the detection of surfactin. Three separate primer pairs were used for fengycin viz. FEND1-F/FEND1-R, FENA1-F/FENA1-R, and FENB2-F/FENB2-R, capable of detecting 964-bp region corresponding to fengycin D, fengycin A and fengycin B respectively. Zwettermycin A was detected through the use of ZWET-F2/ZWET-R1 primer pair, capable of detecting 1-kb region. The outcome of the study shows that all the eight rhizobacteria possessed biosynthetic genes for the production of bacillomycin D, iturin A, and surfactin, however, neither the three types of fengycin nor the zwettermycin A were detected. Sequenced data of these antibiotics have been deposited with GenBank and the following accession numbers assigned to bacillomycin D (MW263002-MW263009), iturin A (MW263010-MW263017), and surfactin (MW263018-MW263025). All the eight rhizobacteria tested were found to possess three out of the five biosynthetic genes namely bacillomycin D, iturin A and surfactin. The detection of these biosynthetic genes confirms and justify why these rhizobacteria are potential biocontrol agents of plant pathogens. }, year = {2023} }
TY - JOUR T1 - Molecular Detection of Biosynthetic Genes for Anti-fungal Metabolite Production by Yam (Dioscorea sp.) Rhizobacteria AU - Larbi-Koranteng Stephen AU - Awuah Tuyee Richard AU - Quain Marian Dorcas AU - Kankam Frederick AU - Muntala Abdulai AU - Yükselbaba Utku Y1 - 2023/11/17 PY - 2023 N1 - https://doi.org/10.11648/j.plant.20231104.12 DO - 10.11648/j.plant.20231104.12 T2 - Plant JF - Plant JO - Plant SP - 122 EP - 129 PB - Science Publishing Group SN - 2331-0677 UR - https://doi.org/10.11648/j.plant.20231104.12 AB - Biosynthetic genes are responsible for antibiotic production by rhizobacterial antagonists. Detection of antibiotic biosynthetic genes of an antagonist is therefore important for the identification of genes and antibiotics responsible for disease suppression. The study was carried out to detect the antibiotic producing genes of eight rhizobacteria responsible for fungal disease suppression. Eight yam (Dioscorea sp.) rhizobacterial isolates which were found to possess antifungal properties against several plant pathogenic fungi and identified as Bacillus species were tested for the presence of genes for biosynthesis of antifungal lipopeptides; bacillomycin D, iturin A, surfactin, fengycin, and aminopolyols, zwettemycin A as possible antibiotic tools for biocontrol using specific primers. The detection of bacillomycin D gene by PCR amplification, gene sequencing, and BLAST analysis, was achieved through the use of the primer pair, BACC1-F/BACC1-R, capable of detecting 875-bp region, iturin A through the use of ITUD1-F/ITUD1-R primer pair, capable of detecting 647-bp region while primer pair SUR3-F/SUR3-R, capable of detecting 441-bp region was also used for the detection of surfactin. Three separate primer pairs were used for fengycin viz. FEND1-F/FEND1-R, FENA1-F/FENA1-R, and FENB2-F/FENB2-R, capable of detecting 964-bp region corresponding to fengycin D, fengycin A and fengycin B respectively. Zwettermycin A was detected through the use of ZWET-F2/ZWET-R1 primer pair, capable of detecting 1-kb region. The outcome of the study shows that all the eight rhizobacteria possessed biosynthetic genes for the production of bacillomycin D, iturin A, and surfactin, however, neither the three types of fengycin nor the zwettermycin A were detected. Sequenced data of these antibiotics have been deposited with GenBank and the following accession numbers assigned to bacillomycin D (MW263002-MW263009), iturin A (MW263010-MW263017), and surfactin (MW263018-MW263025). All the eight rhizobacteria tested were found to possess three out of the five biosynthetic genes namely bacillomycin D, iturin A and surfactin. The detection of these biosynthetic genes confirms and justify why these rhizobacteria are potential biocontrol agents of plant pathogens. VL - 11 IS - 4 ER -