scholarly journals Potencial do óleo essencial de erva-luísa (Aloysia citriodora Palau) no controle de Fusarium sp. in vitro

2016 ◽  
Vol 18 (2) ◽  
pp. 558-562 ◽  
Author(s):  
Á.R. FREDDO ◽  
S.M. MAZARO ◽  
M.S.R. BORIN ◽  
C. BUSSO ◽  
F.E. CECHIN ◽  
...  
Keyword(s):  
Fusarium Sp

RESUMO O presente trabalho teve como objetivo principal avaliar o potencial do uso do óleo essencial de Aloysia citriodora no controle in vitro de Fusarium sp., isolado de plântulas de beterraba infectadas com o mesmo. O trabalho foi realizado por meio de dois experimentos: um sobre o efeito do óleo essencial no crescimento micelial, e outro sobre o efeito na germinação de conídios do fungo. No primeiro trabalho, avaliou-se em delineamento inteiramente ao acaso, o efeito das concentrações 0,0155%; 0,0315%; 0,0625%; 0,125%; 0,250% e 0,500% do óleo essencial de A. citriodora em placas de Petri® com meio de cultivo BDA, mais a testemunha, com meio BDA puro. Cada placa foi considerada uma repetição, as quais foram incubadas a 24ºC±1ºC e submetidas a fotoperíodo de doze horas. Avaliou-se o crescimento radial do patógeno em função do crescimento micelial do patógeno quando este atingia as bordas da primeira placa. No segundo experimento, as mesmas concentrações foram testadas, nas mesmas condições de incubação, no entanto, em lâminas de microscopia com meio BD. Utilizou-se delineamento inteiramente ao acaso, sendo considerada como unidade experimental cada lâmina utilizada. Avaliou-se 24 horas após a incubação, em microscópio óptico, a germinação dos primeiros vinte conídios visualizados a partir do canto esquerdo superior para o direito. Os resultados do segundo experimento foram expressos em porcentagem de germinação de conídios. Os resultados obtidos permitiram concluir que este óleo essencial possui efeito fungistático e fungicida sobre o crescimento micelial e na germinação de conídios de Fusarium sp.. Além disso este efeito é maior em função do aumento da concentração do óleo essencial.

Biocontrol of seed-borne Alternaria raphani and A. brassicicola

1987 ◽  
Vol 33 (10) ◽  
pp. 850-856 ◽  
Author(s):  
G. Vannacci ◽  
G. E. Harman
Keyword(s):  
Biological Control ◽  
Host Range ◽  
Trichoderma Harzianum ◽  
Pythium Species ◽  
Biological Control Agents ◽  
Fusarium Sp ◽  
Chamber Studies ◽  
Growth Chamber Studies ◽  
Radish Seedlings

Forty-two microorganisms were tested as biological control agents against Alternaria raphani and A. brassicicola. Tests were conducted for in vitro antagonistic ability, for ability to control the pathogens on naturally infected seeds germinated on moistened blotters, and in planting mix in growth chamber studies, and for their ability to reduce pod infection. The organisms tested were obtained from cruciferous seeds or were strains already identified as being effective against soil-borne Pythium species. The blotter test indicated that six organisms increased both the number of healthy seedlings and the number of seedlings produced from A. raphani infected radish seeds. An additional seven strains improved either germination or increased the number of healthy seedlings. Twenty-nine organisms increased the number of healthy cabbage seedlings from A. brassicicola infected seeds, but total germination was not modified by any treatment. Experiments in planting mix showed that five antagonists (Chaetomium globosum, two strains of Trichoderma harzianum, T. koningii, and Fusarium sp.) increased the number of healthy plants in both radish samples tested, while four additional antagonists provided a significant increase in only one of the samples tested. The five antagonists that consistently increased numbers of healthy radish seedlings also decreased pod infection by A. raphani. None were as effective as iprodrone, however. Several effective antagonists were found to be mycoparasitic against Alternaria spp. Some strains of Trichoderma previously found to be effective against Pythium spp. were also effective against Alternaria spp., indicating that these strains have a wide host range.

scholarly journals Rizobactérias e alface: colonização rizosférica, promoção de crescimento e controle biológico

2006 ◽  
Vol 30 (2) ◽  
pp. 225-234 ◽  
Author(s):  
Adriana Nanô Sottero ◽  
Sueli dos Santos Freitas ◽  
Arlete Marchi Tavares de Melo ◽  
Paulo Espíndola Trani
Keyword(s):  
Pseudomonas Spp ◽  
Fusarium Sp

Rizobactérias promotoras do crescimento de plantas (RPCPs) podem aumentar a produção agrícola de diversas culturas. O objetivo deste trabalho foi relacionar a colonização radicular e, ou, do colo de plântulas por RPCPs, avaliada in vitro, com sua capacidade de promoção do crescimento, de maneira a agilizar os testes de seleção de isolados de rizobactérias. Além disso, testou-se o antagonismo in vitro entre as bactérias e o fungo Fusarium sp., para verificar a possibilidade de ser a promoção do crescimento exercida por controle biológico de fitopatógeno. Avaliaram-se 64 isolados de rizobactérias do grupo fluorescente de Pseudomonas spp., de diversas origens. A avaliação foi feita visualmente, considerando-se que a presença de uma névoa turva de aspecto esbranquiçado ao longo e em volta da raiz ou de névoa em volta do colo da plântula indicava a colonização das raízes pela bactéria. De todos os isolados bacterianos, apenas oito resultaram em névoa ao longo das raízes e trinta e oito colonizaram a região do colo. Desenvolveu-se também um experimento em casa de vegetação para verificar a capacidade desses isolados de promover crescimento em plantas de alface. O substrato utilizado foi formado por uma mistura de solo e esterco de galinha, semelhante ao usado pelos produtores. Doze isolados promoveram o crescimento das plantas, tendo quatro aumentado a massa de matéria seca da raiz e nove, o número de folhas. Onze isolados que promoveram o crescimento das plantas de alface apresentaram colonização radicular na região do colo. No teste de antagonismo in vitro em meio B de King e em meio BDA, doze dos sessenta e quatro isolados avaliados apresentaram antagonismo contra Fusarium sp., e, desses, apenas três foram eficientes na promoção de crescimento de plantas de alface, tendo colonizado a região do colo das plântulas.

scholarly journals Potensi Metabolit Sekunder Cendawan Endofit Tanaman Cabai sebagai Penghambat Fusarium sp. Patogen Asal Biji Secara in Vitro

2016 ◽  
Vol 12 (1) ◽  
pp. 1-8
Author(s):  
Dewi Novina Sukapiring ◽  
◽  
Bonny Poernomo Wahyu Soekarno ◽  
Titiek Siti Yuliani ◽  
◽  
...  
Keyword(s):  
Fusarium Sp

scholarly journals Actividad antifúngica de propóleos obtenidos en tres provincias de Cuba sobre hongos contaminantes en cultivo de tejidos vegetales

2014 ◽  
Vol 23 (6) ◽  
pp. 3-9
Author(s):  
René Dionisio Cupull-Santana ◽  
Remigio Cortés-Rodríguez ◽  
Ervelio Eliseo Olazábal-Manso ◽  
Carlos Alberto Hernández Medina
Keyword(s):  
Apis Mellifera ◽  
Penicillium Sp ◽  
Trichoderma Sp ◽  
Fusarium Sp ◽  
Aspergillus Sp

La investigación se realizó con el objetivo de evaluar las características fisicoquímicas y la actividad antifúngica de propóleos de Apis mellifera, provenientes de las provincias de Villa Clara, Cienfuegos y Sancti Spíritus, Cuba. Se utilizó el método de recolección por raspado y se estableció el contenido de cera, ceniza, material insoluble y resina de los propóleos crudos. Además, se evaluó la actividad antimicrobiana in vitro frente a los hongos Aspergillus sp., Penicillium sp., Fusarium sp., Trichoderma sp., Colletotrichum sp. y Monilia sp.; los extractos presentaron alta actividad antifúngica en un amplio rango de concentraciones; además, los parámetros fisicoquímicos presentaron valores semejantes y dentro de los establecidos por regulaciones internacionales.

scholarly journals Saprophytic microorganisms with potential for biological control of Botrytis cinerea on Geraldton waxflower flowers

2001 ◽  
Vol 41 (5) ◽  
pp. 697 ◽  
Author(s):  
D. R. Beasley ◽  
D. C. Joyce ◽  
L. M. Coates ◽  
A. H. Wearing
Keyword(s):  
Botrytis Cinerea ◽  
Mycelial Growth ◽  
Germ Tube ◽  
Conidial Germination ◽  
Pseudomonas Sp ◽  
Trichoderma Spp ◽  
Fusarium Sp ◽  
Flower Abscission ◽  
Germ Tube Elongation

Saprophytic bacteria, yeasts and filamentous fungi were isolated from Geraldton waxflower flowers and screened to identify potential antagonism towards Botrytis cinerea. Isolates from other sources (e.g. avocado) were also tested. Isolates were initially screened in vitro for inhibition of B. cinerea conidial germination, germ tube elongation and mycelial growth. The most antagonistic bacteria, yeasts and fungi were selected for further testing on detached waxflower flowers. Conidia of the pathogen were mixed with conidia or cells of the selected antagonists, co-inoculated onto waxflower flowers, and the flowers were sealed in glass jars and incubated at 20˚C. The number of days required for the pathogen to cause flower abscission was determined. The most antagonistic bacterial isolate, Pseudomonas sp. 677, significantly reduced conidial germination and retarded germ tube elongation of B. cinerea. None of the yeast or fungal isolates tested was found to significantly reduce conidial germination or retard germ tube elongation, but several significantly inhibited growth of B. cinerea. Fusarium sp., Epicoccum sp. and Trichoderma spp. were the most antagonistic of these isolates. Of the isolates tested on waxflower, Pseudomonas sp. 677 was highly antagonistic towards B. cinerea and delayed waxflower abscission by about 3 days. Trichoderma harzianum also significantly delayed flower abscission. However, as with most of the fungal antagonists used, inoculation of waxflower flowers with this isolate resulted in unsightly mycelial growth.

scholarly journals In Vitro Inhibition of Fungal Antagonists on Fusarium sp., the Disease Causative Agent on Dragon Fruit Plant (Hylocereus undatus (Haw.) Britton & Rose)

2018 ◽  
Vol 5 (2) ◽  
pp. 224
Author(s):  
Dewa Ayu Andriastini ◽  
Yan Ramona ◽  
Meitini Wahyuni Proborini
Keyword(s):  
Causative Agent ◽  
Biocontrol Agent ◽  
Antagonistic Activity ◽  
Assay Method ◽  
In Vitro Growth ◽  
Dragon Fruit ◽  
Fusarium Sp ◽  
In Vitro Inhibition ◽  
Hylocereus Undatus

A research on in vitro inhibition of fungal antagonists, isolated from dragon fruit plantation in Sembung village, Bali, on Fusarium sp. (the disease causative agent of dragon fruit plant) was conducted with the main objective to investigate the effectiveness of these fungal antagonists to inhibit the in vitro growth of the pathogen. Dual assay method was applied in this experiment. The results showed that three potential fungal antagonists were successfully isolated in this research and they were identified as Trichoderma harzianum, Aspergillus niger, dan Paecilomyces lilacinus. All these fungal antagonists showed antagonistic activity against Fusarium sp. which was statistically significant (p<0.05) when compared to control. This indicated that all antagonist isolates were potential to be developed as biocontrol agent candidates.

Fusarihexins A and B: Novel Cyclic Hexadepsipeptides from the Mangrove Endophytic Fungus Fusarium sp. R5 with Antifungal Activities

Planta Medica ◽  
2018 ◽  
Vol 84 (18) ◽  
pp. 1355-1362 ◽  
Author(s):  
Xinwei Zhu ◽  
Yu Zhong ◽  
Zihui Xie ◽  
Manlin Wu ◽  
Zhibo Hu ◽  
...  
Keyword(s):  
Endophytic Fungus ◽  
Fruits And Vegetables ◽  
Pathogenic Fungi ◽  
Crown Rot ◽  
Fruit Rot ◽  
Chemical Structures ◽  
Mangrove Endophytic Fungus ◽  
Fusarium Sp ◽  
Colletotrichum Musae

AbstractTwo novel cyclic hexadepsipeptides, fusarihexin A (1) and fusarihexin B (2), and two known compounds, cyclo-(L-Leu–L-Leu–D-Leu–L-Leu–L-Val) (3) and cyclo-(L-Leu–L-Leu–D-Leu–L-Leu–L-Ile) (4), were isolated from the marine mangrove endophytic fungus Fusarium sp. R5. Their chemical structures were elucidated on the basis of spectroscopic data and Marfeyʼs analysis. In an in vitro bioassay, fusarihexin A (1) remarkably inhibited three plant pathogenic fungi: Colletotrichum gloeosporioides (Penz.) Sacc., which causes anthracnose in many fruits and vegetables, Colletotrichum musae (Berk. and M. A. Curtis) Arx, which causes crown rot and anthracnose in bananas, and Fusarium oxysporum Schlecht. f. sp. lycopersici (Sacc.) W. C. Snyder et H. N. Hansen, which causes Fusarium wilt and fruit rot in tomatoes. Fusarihexin B (2) strongly inhibited C. gloeosporioides and C. musae. The compounds were more potent than carbendazim, which is widely used as an agricultural and horticultural fungicide worldwide.

scholarly journals Salicylic acid in the induction of resistance to beet seedling damping-off and antifungal activity against Fusarium sp., in vitro

2016 ◽  
Vol 37 (1) ◽  
pp. 67 ◽  
Author(s):  
Douglas Junior Bertoncelli ◽  
Sérgio Miguel Mazaro ◽  
Rita De Cacia Dosciatti Serrão Rocha ◽  
Nean Locatelli Dalacosta ◽  
Adriano Lewandowski ◽  
...  
Keyword(s):  
Salicylic Acid ◽  
Antifungal Activity ◽  
Mycelial Growth ◽  
Experimental Unit ◽  
Damping Off ◽  
Potato Dextrose Agar Medium ◽  
Seedling Length ◽  
Fusarium Sp ◽  
And Control

The damping off is the main disease that affects the beet crop during the seedling production. The aim of this study was to evaluate different salicylic acid (SA) concentrations for resistance induction against damping-off in beet seedling and its antifungal activity against Fusarium sp., in vitro condition. Treatment of beet seed was with SA solution by immersion during 5 minutes in the 0.5, 1.0, 1.5 and 2.0 mM concentrations and control (distilled water). It was used four replications with 20 cells by experimental unit. The experiment was carried out for 14 days in cultivate chamber with temperature (23 oC ± 2°C), lighting (12 hours photoperiod) and humidity (70% ± 10%) controlled. After this time, the germination, damping off incidence, seedling length and fresh mass matter weight were evaluated. It was evaluated also in the seedling tissue the phenylalanine ammonia-lyase (PAL), ?-1.3 glucanase and chitinase level enzymes. In the in vitro the SA was putted in PDA (potato-dextrose-agar) medium, where the Fusarium sp. mycelial growth was evaluated. The SA applied for seeds treatment didn’t had effect significant on damping off of beet seedlings, but it induced the activity of ?-1.3 glucanase enzyme, it being this higher in nine times when compared the treatment control. The SA acted in the Fusarium sp. in vitro control with fungitoxic action, suppressed mycelial growth in 28% if compared to control.

scholarly journals Identifikasi Senyawa Aktif Kulit Batang Ampupu (Eucalyptus alba Reinw. Ex. Blume) dalam Menghambat Pertumbuhan Jamur Fusariummoniliforme

2018 ◽  
Vol 3 (01) ◽  
pp. 11-13
Author(s):  
Bernadina Metboki
Keyword(s):  
Tert Butyl ◽  
Alpha Pinene ◽  
Fusarium Sp

Produksi jagung yang rendah di Indonesia disebabkan oleh banyak faktor salah satunya adalah penyakit yang disebabkan oleh jamur. Pengendalian jamur dengan menggunakan bahan kimia sangat berbahaya bagi kesehatan. Oleh karena itu, diperlukan usaha pengembangan fungisida nabati yang ramah lingkungan, misalnya dengan menggunakan ekstrak kulit batang ampupu. Tujuan penelitian untuk mengetahui efek anti jamur dari ekstrak kulit batang ampupu terhadap pertumbuhan jamur Fusarium sp. yangmenyebabkan busuk tongkoljagung. Pengujian hambatan pertumbuhan Fusarium sp. oleh ekstrak kulit batang ampupu dilakukan di laboratorium dengan metode sumur difusi pada media PDA. Ekstrak dengan konsentrasi 1,5%, 3,0%, 4,5% di masukkan dalam sumur difusi pada setiap petri. Identifikasi senyawa aktif menggunakan Kromatografi Gas-Spektroskopi Massa.Hasil penelitian menunjukkan bahwa secara in vitro ekstrak kasar kulit batang ampupu dengan konsentrasi 1,5%, 3,0%, dan 4,5% mampu menghambat pertumbuhan jamur Fusarium moniliformedengan diameter zona hambatan masing-masing adalah 0,18 mm, 1,85 mm, 2,01 mm. peningkatan konsentrasi ekstrak yang diberikan menyebabkan zona hambatan yang terbentuk lebih besar. Sebelas senyawa dalam ekstrak methanol kulit batang ampupu diketahui berpotensi sebagai anti jamur yaitu Ethylbenzene, o-Xylene, ALPHA.-PINENE,DELTA.3-Carene, Azulene(CAS)Cyclopentacycloheptene, Tetradecane(CAS)n-Tetradecane, 2,6-Diisopropylnaphthalene, 7,9-Di-tert-butyl-1-oxaspiro(4,5)deca-6,9-dien, Hexadecanamide, 9-Octadecenamide, (Z)-(CAS)OLEOAMIDE, 1,2-Benzenedicarboxylicacid,mono(2-ethylhexyl). ©2018 dipublikasikan oleh Savana Cendana.

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