Please use this identifier to cite or link to this item: https://repository.unej.ac.id/xmlui/handle/123456789/89800
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dc.contributor.authorAsyiah, Iis Nur-
dc.contributor.authorHindersah, Reginawanti-
dc.contributor.authorHarni, Rita-
dc.date.accessioned2019-03-13T07:30:27Z-
dc.date.available2019-03-13T07:30:27Z-
dc.date.issued2019-03-13-
dc.identifier.isbn978-0-7354-1619-2-
dc.identifier.urihttp://repository.unej.ac.id/handle/123456789/89800-
dc.descriptionProceeding The 1st International Conference and Exhibition on Powder Technology Indonesia (ICePTi) 2017en_US
dc.description.abstractRoots of food crops are colonized by nonpathogenic mycorrhizal fungi which show natural ability to control plant pathogen. Mycorrhizal establishment in plant roots is affected by rhizobacteria, known as mycorrhiza helper bacteria (MHB), which has synergetic effects on mycorrhizal associations. Laboratory experiment has been conducted to assess the best carrier material to develop well-qualified MHB of Pseudomonas diminuta and Bacillus subtilis solid inoculant. Carrier materials were 100 mesh organic matter of agricultural waste. Different spore concentration of both bacterial liquid inoculants were grown on three kinds of 100-mesh organic matter and stored at room temperature up to 90 days. Cell viability of both MHB were counted by serial dilution plate method by using specific medium. The results showed that sugar cane baggase ash was the best carrier material to maintain cell viability for both MHB. However, the population of Pseudomonas diminuta and Bacillus subtilis in sugar cane baggase ash were slightly decreased after 90 days. The use of sugarcane baggase ash for solid MHB inoculant development could be suggested.en_US
dc.language.isoenen_US
dc.subjectCell Viabilityen_US
dc.subjectMycorrhiza Helper Bacteriaen_US
dc.subjectMHBen_US
dc.titleCell Viability of Mycorrhiza Helper Bacteria Solid Inoculant in Different Carrier Materialen_US
dc.typeProsidingen_US
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