2009
DOI: 10.1016/j.micres.2006.11.022
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Quantitative isolation of biocontrol agents Trichoderma spp., Gliocladium spp. and actinomycetes from soil with culture media

Abstract: Soil biodiversity plays a key role in the sustainability of agriculture systems and indicates the level of health of soil, especially when considering the richness of microorganisms that are involved in biological control of soilborne diseases. Cultural practices may produce changes in soil microflora, which can be quantified through the isolation of target microorganisms. Rhizosphere soil samples were taken from an assay with different crop rotations and tillage systems, and populations of Trichoderma spp., G… Show more

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Cited by 122 publications
(45 citation statements)
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“…After sterilization in 1% NaOCl for 2 min, the roots were washed with sterile distilled water, weighed, and homogenized using an ULTRA-TURRAX apparatus (Janke & Kunkel) in 20 mL of water for 1 min. Serial dilutions were plated for colony forming unit counts on Trichoderma selective medium (Vargas Gil et al, 2008) at 28°C.…”
Section: Root Colonization Assaymentioning
confidence: 99%
“…After sterilization in 1% NaOCl for 2 min, the roots were washed with sterile distilled water, weighed, and homogenized using an ULTRA-TURRAX apparatus (Janke & Kunkel) in 20 mL of water for 1 min. Serial dilutions were plated for colony forming unit counts on Trichoderma selective medium (Vargas Gil et al, 2008) at 28°C.…”
Section: Root Colonization Assaymentioning
confidence: 99%
“…After the last disease evaluation, a dilution plate count technique (Vargas Gil et al 2009) was performed, taking 10 g of soil from each pot and diluting them in 90 mL of tap water. After agitation for 90 min at 170 rpm, a serial dilution was made to 1 g L -1 .…”
Section: Methodsmentioning
confidence: 99%
“…After 48 h of interaction, seedlings were transferred to individual plastic pots (56565 cm) containing sterilized peat moss soil (S-Jord; Hasselfors Garden) and the B. cinerea bioassay was performed following the procedure described previously (Dubey et al, 2013). To recover the T. atroviride strains, plants were carefully removed from the pots, after washing in water the roots were surface sterilized with 1 % NaOCl for 5 min and placed in Rose Bengal medium (Vargas Gil et al, 2009). The bioassay experiment was performed with five biological replicate and each replicate had three plants for each treatment.…”
Section: Construction Of Deletion and Complementation Vectorsmentioning
confidence: 99%