Generic placeholder image

Recent Patents on Food, Nutrition & Agriculture

Editor-in-Chief

ISSN (Print): 2212-7984
ISSN (Online): 1876-1429

Research Article

Antifungal Mechanism of Rhodotorula mucilaginosa and Aureobasidium sp. nov. Isolated from Cerbera manghas L. against the Growth of Destructive Molds in Post Harvested Apples

Author(s): Dalia Sukmawati*, Andisa Shabrina, Reni Indrayanti, Tri Handayani Kurniati, Muktiningsih Nurjayadi, Iman Hidayat, Shabrina Nida Al Husna, Nuniek Ina Ratnaningtyas, Hesham El Enshasy, Daniel Joe Dailin and Abd El-Latif Hesham

Volume 11, Issue 3, 2020

Page: [219 - 228] Pages: 10

DOI: 10.2174/2212798411666200423101159

Abstract

Background: Apples often experience postharvest damage due to being attacked by mold organisms. Several groups of molds such as Aspergillus sp., Penicilium expansum, Botrytis cinerea, and Venturia sp. can cause a serious postharvest disease exhibited as watery regions where areas of blue-green tufts of spores develop. Current methods using fungicides to control pathogenic fungi can cause resistance if applied in the long term. An alternative procedure using yeast as a biological agent has been found.

Objective: The aim of this study is to screen potential yeast, which has the ability to inhibit the growth of Aspergillus brasielensis (isolate A1) and Aspergillus flavus section flavi (isolate A17) isolated from apple fruits.

Methods: Antagonism test using YMA dual culture medium using in vitro assays and ITS rDNA identification were performed.

Results: The result showed that 3 out of 19 yeast isolated from Cerbera manghas L, T1, T3 and T4, demonstrated the potential ability as a biocontrol agent. ITS rDNA identification demonstrated that T1 has a similarity to Rhodotorula mucilaginosa while T3 and T4 were identified as Aureobasidium sp. nov. The 3 isolates exhibited the ability to reduce the growth of A. brasiliensis sensu lato better than dithane 0.3% with a Disease Incidence (DI) of 100% and a Disease Severity (DS) value of 45%. Only isolate T1 and T3 were able to reduce decay symptoms in apples inoculated with A. flavus sensu lato (with DO and DS were 100% and 25%, respectively) compared to dithane pesticides 0.3%.

Conclusion: This study indicated that competition between nutrients occurs between pathogenic molds and under-yeast in vitro and in vivo conditions. However, further studies in the future might be able to elucidate the ‘killer’ activity and interaction with the pathogen cells and the bio-product production using Rhodotorula mucilaginosa and Aureoubasidium namibiae strains to control postharvest diseases.

Keywords: Apple, Aureobasidium pullulans, biocontrol fungi, Rhodotorula mucilaginosa, molds, fungicides.

Graphical Abstract
[1]
Wulandari A. Antibacterial ability of manalagi apple extracts against Salmonella thyposa. J Healthy Sci AAKMAL 2002; 2: 1-3.
[2]
Oro L, Feliziani E, Ciani M, Romanazzi G, Comitini F. Volatile organic compounds from Wickerhamomyces anomalus, Metschnikowia pulcherrima and Saccharomyces cerevisiae inhibit growth of decay causing fungi and control postharvest diseases of strawberries. Int J Food Microbiol 2018; 265: 18-22.
[http://dx.doi.org/10.1016/j.ijfoodmicro.2017.10.027] [PMID: 29107842]
[3]
Donowarti I, Winahyu ST. Economic analysis of apple production in Poncokusumo village, Malang Regency. Primordia 2008; 4(2): 150-6.
[4]
Semangun H. Horticultural Crop Diseases in Indonesia. 3rd ed. Gajah Mada University Press Yogyakarta 2007.
[5]
Aladdin A, Dib JR, Abd MR, Enshasy HE. Killer Yeast, a Novel Biological Control of Soilborne Diseases for Good Agriculture Practice. In: Zakaria ZA, Ed. Sustainable Technologies for the Management of Agricultural Wastes. Singapore: Springer 2018: 71-86..
[http://dx.doi.org/10.1007/978-981-10-5062-6_6]
[6]
Maxin P, Williams M, Weber RWS. Control of fungal storange rots of apples by hot water treatments: a northern Eurpoean perspective. Erwerbs-Obstbau 2014; 56: 25-34.
[http://dx.doi.org/10.1007/s10341-014-0200-z]
[7]
da Cunha T, Ferraz LP, Wehr PP, Kupper KC. Antifungal activity and action mechanisms of yeasts isolates from citrus against Penicillium italicum. Int J Food Microbiol 2018; 276: 20-7.
[http://dx.doi.org/10.1016/j.ijfoodmicro.2018.03.019] [PMID: 29653393]
[8]
Santoso B. Postharvest Diseases of Horticultural Commodities. Rineka Cipta Jakarta 2008.
[9]
Vico I, Duduk N, Vasic M. Identification of Penicillium expansum causing postharvest blue mold decay of apple fruit Pestic phytomedicina 2014; 29(4): 257-66.
[10]
Soemirat J. Environmental Toxicology. Gadjah Mada University Press Yogyakarta 2003.
[11]
Mahyuni EL. Risk factors in the use of pesticides for health complaints to farmers in Berastagi District, Karo Regency. Kesmas 2015; 9: 79-89.
[12]
Abdel-Aziz SM, Gupta VK, Sukmawati D, Fadel M. Role of nutrient in microbial developments and microbial metabolic diversity. Microbial Applications 2016; 7: 151-76.
[http://dx.doi.org/10.1515/9783110412789-009]
[13]
Enshasy HE, Dailin DJ, Manas NHA, et al. Current and future applications of phytases in poultry industry: a critical review. J Adv VetBio Sci Tech 2018; 3(3): 65-74.
[http://dx.doi.org/10.31797/vetbio.455687]
[14]
Sperandio EM, Martins do Vale HM, Moreira GAM. Yeasts from native Brazilian Cerrado plants: occurrence, diversity and use in the biocontrol of citrus green mould. Fungal Biol 2015; 119(11): 984-93.
[http://dx.doi.org/10.1016/j.funbio.2015.06.011] [PMID: 26466874]
[15]
Sukmawati D, Puspitasari SI, Wahyudi P, et al. Screening mold Aspergillus spp. producing aflatoxin in corn pipeline at Bekasi, West Java Area. Al-Kauniyah. J Biol 2018; 11(2): 151-62.
[16]
Yun W, Yulin L, Weidong X, et al. Exploring the effect of β-glucan on the biocontrol activity of Cryptococcus podzolicus against postharvest decay of apples and the possible mechanisms involved. Biol Control 2018; 121: 14-22.
[http://dx.doi.org/10.1016/j.biocontrol.2018.02.001]
[17]
Golubev WI. Antagonistic Anteractions among yeast. In: Peter G, Rosa C, Eds. Biodiversity and Ecophysiology of Yeasts. Germany: Springer 2006: 197-219..
[18]
Lopes MR, Klein MN, Ferraz LP, da Silva AC, Kupper KC. Saccharomyces cerevisiae: a novel and efficient biological control agent for Colletotrichum acutatum during pre-harvest. Microbiol Res 2015; 175: 93-9.
[http://dx.doi.org/10.1016/j.micres.2015.04.003] [PMID: 25960430]
[19]
Sukmawati D. Antagonism mechanism of fungal contamination animal feed using phylloplane yeasts isolated from the Bintaro plant (Cerbera manghas) Bekasi in Java, Indonesia. Int J Curr Microbiol Appl Sci 2016; 5(5): 54-62.
[http://dx.doi.org/10.20546/ijcmas.2016.505.007]
[20]
Perez MF, Isas AS, Aladdin A, Enshasy HE, Dib JR. Killer Yeasts as Biocontrol Agents of Postharvest Fungal Diseases in Lemons. In: Zakaria ZA, Ed. Sustainable Technologies for the Management of Agricultural Wastes. Singapore: Springer 2018: 87-98..
[http://dx.doi.org/10.1007/978-981-10-5062-6_7]
[21]
Spadaro D. Biological control of postharvest diseases of pome fruit using yeast antagonist PhD Thesis, University of Turin, Turin, Italy, 2003.
[22]
Widyastuti S. Post harvest diseases control of Penicillium expansum against yeast Rhodotorula glutinis. Proceedings of Agricultural Engineering National Seminar. Yogyakarta. 2008.
[23]
Liu Y, Wang W, Zhou Y, Yao S, Deng L, Zeng K. Isolation, identification and in vitro screening of Chongqing orangery yeasts for the biocontrol of Penicillium digitatum on citrus fruit. Biol Control 2017; 110: 18-24.
[http://dx.doi.org/10.1016/j.biocontrol.2017.04.002]
[24]
Liu Z, Du S, Ren Y, Liu Y. Biocontrol ability of killer yeasts (Saccharomyces cerevisiae) isolated from wine against Colletotrichum gloeosporioides on grape. J Basic Microbiol 2018; 58(1): 60-7.
[http://dx.doi.org/10.1002/jobm.201700264] [PMID: 29105800]
[25]
Wang Y, Luo Y, Sui Y, et al. Exposure of Candida oleophila to sublethal salt stress induces an antioxidant response and improves biocontrol efficacy. Biol Control 2018; 127: 109-15.
[http://dx.doi.org/10.1016/j.biocontrol.2018.09.002]
[26]
James RB. Ed Nutritional control of growth and development in yeast. Genetics 2012; 192(1): 73-105.
[27]
Agrios GN. Plant Pathology. 5th ed. University of Florida Florida 2005.
[28]
Utami S. Insecticide activity of bintaro against Eurema sp. on a labora-tory scale. J Plantation Forest Res 2010; 7(4): 211-0.
[29]
Awad HM, El-Enshasy HA, Hanapi SZ, Hamed ER, Rosidi B. A new chitinase-producer strain Streptomyces glauciniger WICC-A03: isolation and identification as a biocontrol agent for plants phytopathogenic fungi. Nat Prod Res 2014; 28(24): 2273-7.
[http://dx.doi.org/10.1080/14786419.2014.939083] [PMID: 25078877]
[30]
Peréz-Sariñana BY, Fernandoa SEL, Sergio ST, Eapen D, Sebastian PJ. Evaluation of agro-industrial wastes to produce bioethanol: case study - mango (Mangifera indica L.). Energy Procedia 2014; 57: 860-6.
[http://dx.doi.org/10.1016/j.egypro.2014.10.295]
[31]
Hall BG. Phylogenetic trees made easy: A how to manual for molecular biologists. Sinaeur Associates Inc Sunderland 2001.
[32]
Sukmawati D, Oetari A, Hendrayanti D, Atria M, Wellyzar S. Identification of phylloplane yeasts from paper mulberry (Broussonetia papyrifera (L.) L’Her.ex Vent.) in Java, Indonesia. Malays J Microbiol 2015; 11(4): 324-40.
[33]
Shabrina A, Sukmawati D, Hidayat I. Isolation and pathogenicity test of destructive molds in Malang apples (Malus sylvestris Mill.) post harvest. Bioma 2018; 14(1): 4.
[34]
Sibounnavong P, Soytong K, Divina CC, Kalaw SP. In-vitro biological activities of Emericella nidulans, a new fungal antagonist, against Fusarium oxysporum f. sp. lycopersici. J Agr Technol 2009; 5(1): 75-84.
[35]
Tang YC, Amon A. Gene copy number alterations: a cost-benefit analysis 2013; 152: 394-405..
[http://dx.doi.org/10.1016/j.cell.2012.11.043]
[36]
Mahunu GK, Zhang H, Yang Q, Zhang X, Li D, Zhou Y. Improving the biocontrol efficacy of Pichia caribbica with phytic acid against postharvest blue mold and natural decay in apples. Biol Control 2015; 92: 172-89.
[http://dx.doi.org/10.1016/j.biocontrol.2015.10.012]
[37]
Wan M, Li G, Zhang J, Jiang D, Huang HC. Effect of volatile substances of Steptomyces platensis F-1 on control of plant fungal diseases. Biol Control 2008; 46: 552-9.
[http://dx.doi.org/10.1016/j.biocontrol.2008.05.015]
[38]
White TJ, Bruns T, Lee S, Taylor JW. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, Eds. PCR Protocols. New York: Academic Press Inc 1990: 315-22..
[http://dx.doi.org/10.1016/B978-0-12-372180-8.50042-1]
[39]
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol 1990; 215(3): 403-10.
[http://dx.doi.org/10.1016/S0022-2836(05)80360-2] [PMID: 2231712]
[40]
Hidayat T, Pancoro A. Molecular phylogenetic studies and its role in providing basic information for improving the quality of orchid genetic sources. J Agro Biogen 2008; 4: 35-40.
[41]
Lutz C, Gramisci BR, Lutz MC, Lopes CA, Sangorrín MP. Enhancing the efficacy of yeast biocontrol agents against postharvest pathogens through nutrient profiling and the use of other additives. Biol Control 2018; 121: 151-8.
[http://dx.doi.org/10.1016/j.biocontrol.2018.03.001]
[42]
Janisiewicz WJ, Korsten L. Biological control of postharvest diseases of fruits. Annu Rev Phytopathol 2002; 40: 411-41.
[http://dx.doi.org/10.1146/annurev.phyto.40.120401.130158] [PMID: 12147766]
[43]
Sharma RR, Singh D, Singh R. Biological control of postharvest diseases of fruits and vegetables by microbial antagonists: a review. Biol Control 2009; 50: 205-21.
[http://dx.doi.org/10.1016/j.biocontrol.2009.05.001]
[44]
Vermeersch L, Perez-Samper G, Cerulus B, et al. On the duration of the microbial lag phase. Curr Genet 2019; 65(3): 721-7.
[http://dx.doi.org/10.1007/s00294-019-00938-2] [PMID: 30666394]
[45]
Mahreni SS, Ferlany I. Agustina. Production of (Sacharomyces cerevisiae) (Fncc-3049) in The Flour of Banana Skin Culture in The Aerobic Condition. The 1st ACIKITA International Conference of Science and Technology. 2 February 2011..
[46]
Asaduzzaman MD. Standardization of yeast growth curves from several curves with different initial sizesMaster’s Thesis, University of Technology and Goteborg University SE, Goteborg, Sweden, 2007.
[47]
Iriani S, Maria B, Nur M. Potentially antihyperglycemic from biomass and phycocyanin of Spirulina fusiformis Voronikhin by in vivo test. Procedia Chem 2015; 14: 211-5.
[http://dx.doi.org/10.1016/j.proche.2015.03.030]
[48]
James SA, Collins MD, Roberts IN. Use of an rDNA internal transcribed spacer region to distinguish phylogenetically closely related species of the genera Zygosaccharomyces and Torulaspora. Int J Systemastic Bacteriol 1996; 46(1): 180-94.
[49]
Becker B, Schmitt MJ. Yeast killer toxin k28: biology and unique strategy of host cell intoxication and killing. Toxins 2017; 9(10): 333.
[http://dx.doi.org/10.3390/toxins9100333] [PMID: 29053588]
[50]
Ferraz LP, Cunha TD, da Silva AC, Kupper KC. Biocontrol ability and putative mode of action of yeasts against Geotrichum citri-aurantii in citrus fruit. Microbiol Res 2016; 188-189: 72-9.
[http://dx.doi.org/10.1016/j.micres.2016.04.012] [PMID: 27296964]
[51]
Jalal G, Etebarian HR, Sahebani NA, Roustaee A. Characterization of biocontrol activity of two yeast strains from iran against blue mould of apple in order to reduce the environmental pollution. J Int Environ Appl Sci 2009; 4(1): 28-36.
[52]
Monika W, Kordowska-Wiater M. The occurrence of killer activity in yeasts isolated from natural habitats. Acta Biochimica 2015; 46: 237-46.
[53]
Varga J, Kocsubé S, Tóth B, et al. Aspergillus brasiliensis sp. nov., a biseriate black Aspergillus species with world-wide distribution. Int J Syst Evol Microbiol 2007; 57(Pt 8): 1925-32.
[http://dx.doi.org/10.1099/ijs.0.65021-0] [PMID: 17684283]
[54]
Kozakiewicz Z. Aspergillus species on stored products. Taylor & Francis, Ltd Florida 2008.
[http://dx.doi.org/10.1099/ijs.0.65123-0] [PMID: 18319485]
[55]
Dellanerra D, Risandi A, Anggun S, et al. Screening and characterization of amylolitic mold originated from ghost crab (Ocypode sp) in Cidaon Ujung Kulon National Park, Indonesia AIP Conference Proceedings21202019;
[56]
Sukmawati D, Dellanerra D, Risandi A. Screening the capabilities of Indonesian indigenous mold in producing cellulase enzyme. Mater Sci Eng 2018; 434(1)012125
[http://dx.doi.org/10.1088/1757-899X/434/1/012125]

© 2024 Bentham Science Publishers | Privacy Policy