2016
DOI: 10.1007/s00253-016-7977-7
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Inhibited growth of Clostridium butyricum in efficient H2-producing co-culture with Rhodobacter sphaeroides

Abstract: Cell number of Clostridium butyricum and Rhodobacter sphaeroides in co-culture was measured using q-PCR approach. During efficient H photoproduction from starch (6.2 mol H/mol glucose), Clostridia growth and starch-hydrolyzing activity was partly suppressed. Apparently, the effect of R. sphaeroides towards C. butyricum was not attributed to altered E or pH values in the presence of purple bacteria. Further, disk-diffusion test proved that R. sphaeroides was capable of producing inhibitors against another purpl… Show more

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Cited by 5 publications
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“…The PCR mixture included 10 μL SYBR Premix Ex Taq ™ (Takara Bio Inc., Dalian, China), 0.4 μL ROX Reference Dye II, 0.8 μL (0.4 μM) forward primer and reverse primer, and 6 μL ddH 2 O. The amplification conditions comprised the following steps: at 95 ℃ for 30 s, 40 cycles at 95 ℃ for 5 s, and 60 ℃ for 30 s. The primers used for qPCR amplification are shown in Table 1 (Sun et al 2010 ; Laurinavichene et al 2010 ; Larsen et al 2013 ). Using the Student’s t -test, statistically significant differences between groups were assessed.…”
Section: Methodsmentioning
confidence: 99%
“…The PCR mixture included 10 μL SYBR Premix Ex Taq ™ (Takara Bio Inc., Dalian, China), 0.4 μL ROX Reference Dye II, 0.8 μL (0.4 μM) forward primer and reverse primer, and 6 μL ddH 2 O. The amplification conditions comprised the following steps: at 95 ℃ for 30 s, 40 cycles at 95 ℃ for 5 s, and 60 ℃ for 30 s. The primers used for qPCR amplification are shown in Table 1 (Sun et al 2010 ; Laurinavichene et al 2010 ; Larsen et al 2013 ). Using the Student’s t -test, statistically significant differences between groups were assessed.…”
Section: Methodsmentioning
confidence: 99%