2016
DOI: 10.9755/ejfa.2015-05-195
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Medium optimization of beta-glucanase production by Bacillus subtilis SAHA 32.6 used as biological control of oil palm pathogen

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Cited by 28 publications
(26 citation statements)
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“…Therefore, it can be concluded that the suitable incubation time was established at 52 and 56 hrs for BG15 and BG21, respectively. Compared to previous research by Dewi et al (2016) reported that the strain B. subtilis SAHA 32.6 produced the highest β-glucanase activity in the medium containing 1% β-glucan after 12 hrs of incubation, the culture time of strain BG15 and BG21 was significantly longer.…”
Section: Effect Of Incubation Time On β-Glucanase Production Ability contrasting
confidence: 77%
“…Therefore, it can be concluded that the suitable incubation time was established at 52 and 56 hrs for BG15 and BG21, respectively. Compared to previous research by Dewi et al (2016) reported that the strain B. subtilis SAHA 32.6 produced the highest β-glucanase activity in the medium containing 1% β-glucan after 12 hrs of incubation, the culture time of strain BG15 and BG21 was significantly longer.…”
Section: Effect Of Incubation Time On β-Glucanase Production Ability contrasting
confidence: 77%
“…The bacteria were grown in selective media consisting of different ingredients (g/L) i.e. K 2 HPO 4 (0.065), KH 2 PO 4 117 (0.25), (NH4) 2 SO 4 (0.05), NaCl (0.25), MgSO 4 .7H 2 O (0.012), yeast extract (0.15), 1% Laminarian at 37°C, 130 rpm for 96 h [ 47 ]. The cell free supernatant was obtained as described in section 2.2.1 and used as crude enzyme extract.…”
Section: Methodsmentioning
confidence: 99%
“…The main antagonistic mechanisms of the bacteria and yeasts in vitro against the phytopathogens are the production of hydrolytic enzymes, such as β-1,3-glucanase [38,39], which break the links of the glucan present in the cell wall of the phytopathogen, limiting their germination and growth. This enzyme has already been reported for B. subtilis [40], S. rhizophila [30,41,42], and C. laurentii [43]. The competence for space and nutrients is another mechanism through which the bacteria and yeasts limit phytopathogens in vitro because these microorganisms have a short period of exponential growth that allows them to exhaust carbon sources in their culture medium, thereby minimizing zoospore germination and phytopathogen growth [44,45].…”
Section: Discussionmentioning
confidence: 70%