2017
DOI: 10.15376/biores.12.2.3371-3386
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Production of Acetone, Butanol, and Ethanol (ABE) by Clostridium acetobutylicum YM1 from Pretreated Palm Kernel Cake in Batch Culture Fermentation

Abstract: The viability of most fermentation processes is very much dependent on the cheap fermentation medium used. Palm kernel cake (PKC) is an abundant biomass generated from the palm oil processing industry that can be used as the carbon source for the growth and production of acetone-butanolethanol fermentation (ABE) by Clostridia. In this study, ABE production from the fermentation of PKC using Clostridium acetobutylicum YM1 in a batch culture was conducted. The PKC was subjected to treatment with acids (sulphuric… Show more

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Cited by 10 publications
(11 citation statements)
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“…However, after 36 hr, the cell dry weight no longer increased but instead decreased. This trend could be continuously accumulating results of the nutrient limitation (Burgard et al., ) or production inhibition of metabolites such as ethanol or others (Al‐Tabib, Al‐Shorgani, Hasan, Hamid, & Kalil, ). Although the physical and biochemical environments of the fed‐batch cultivation differ from those of a full cultivation, it is a useful attempt to build Z. rouxii high‐density cultivation.…”
Section: Resultsmentioning
confidence: 99%
“…However, after 36 hr, the cell dry weight no longer increased but instead decreased. This trend could be continuously accumulating results of the nutrient limitation (Burgard et al., ) or production inhibition of metabolites such as ethanol or others (Al‐Tabib, Al‐Shorgani, Hasan, Hamid, & Kalil, ). Although the physical and biochemical environments of the fed‐batch cultivation differ from those of a full cultivation, it is a useful attempt to build Z. rouxii high‐density cultivation.…”
Section: Resultsmentioning
confidence: 99%
“…The injection and detector temperatures were set at 250 °C and 280 °C respectively. Helium gas was used as a carrier gas with a flow rate of 1.50 mL/min (Al-Tabib et al 2017).…”
Section: Methodsmentioning
confidence: 99%
“…Approximately 1 mL of C. acetobutylicum YM1 cells were cultured in 9 mL of TYA medium and were incubated for 1 to 2 days at 30 °C under anaerobic conditions. This culture was subcultured in 90 mL TYA medium and incubated for 18 to 20 h at 30 °C to be used as inoculum (Al-Tabib et al 2017). Before the inoculation process, the nitrogen gas was purged into fermentation medium (TYA medium/fermentable sugars) to prepare the anaerobic conditions for cell growth and BioABE production.…”
Section: Bioabe Fermentationmentioning
confidence: 99%
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