The Hydrolysis of Coconut Kernel Residue by Aspergillus niger, Trichoderma reesei, and Fermentation of Hydrolysate by Saccharomyces cerevisiae for Ethanol Production
Coconut kernel residue are by-product from coconut processing industry, especially in Indonesia as the world’s second largest producer of coconut. Coconut kernel residue has a high cellulose content that could be converted to be a valuable product, such as ethanol. To manifest an integrated cocon...
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Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/34841 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Coconut kernel residue are by-product from coconut processing industry,
especially in Indonesia as the world’s second largest producer of coconut.
Coconut kernel residue has a high cellulose content that could be converted to be
a valuable product, such as ethanol. To manifest an integrated coconut industry,
the study of utilization of coconut kernel residue for ethanol production by
fermentation has been done. The optimization of inocula ratio has been conducted
to obtain the best inocula ratio. The inocula were mixed cultures of Aspergillus
niger and Trichoderma reesei with inocula ratio of 1:0, 0:1, 1:1, 1:2, and 2:1. The
highest reducing sugar equivalent with glucose was 104,27 mg/g by the fourth day
of fermentation, obtained from the substrate inoculated with A.niger : T.reesei
(1:0). A.niger was used as inoculum in hydrolysis process of coconut kernel
residue. The highest reducing sugar was 83,93 mg/g by the second day of
fermentation, and the highest CMCase activity was 612,99 U/g from the sixth day
of fermentation. Hydrolysis of coconut kernel residue by crude enzyme extract of
A.niger produced the highest reducing sugar 139,57 mg/g at the seventh day of
fermentation. At the end of the hydrolysis process, the cellulose content of
coconut kernel residue decreased up to 10,66%. Ethanol fermentation was done by
extracting the coconut kernel residue and inoculated the hydrolysate with
Saccharomyces cerevisiae for seven days. |
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