본 연구는 해조류, 꼬시래기를 발효하여 에탄올을 생산하였다. 최적 전처리 조건은 12% (w/v) 해조류 슬러리, 270 mM 황산, 121도 60분동안 실시하였다. 열산가수분해 후에, 꼬시래기 가수분해산물에 16 U/ml의 혼합효소 Viscozyme L과 Celluclast 1.5 L를 이용하여 효소당화를 수행하였다. 50.4 g/l의총단당류의농도는, 120 g dw/l 꼬시래기 슬러리로부터 열산가수분해와효소당화에 의해 총 탄수화물 60 g/l의 전환율 84.2%를 나타내었다. 꼬시래기 가수분해산물은 분리당화발효(SHF)로 에탄올 생산을 위한 기질로 사용하였다. 고농도 galactose로 순치한 Candida lusitaniae ATCC42720에 의한 에탄올 생산은 0.43의 에탄올 수율(YEtOH)인 22.0 g/l를 생산하였다. 특정 당에 순치한 효모는 혼합당의 흡수에 유용하며, 그 결과 해조류가수분해산물배지로부터 높은 에탄올 수율을 나타내었다.
본 연구는 해조류, 꼬시래기를 발효하여 에탄올을 생산하였다. 최적 전처리 조건은 12% (w/v) 해조류 슬러리, 270 mM 황산, 121도 60분동안 실시하였다. 열산가수분해 후에, 꼬시래기 가수분해산물에 16 U/ml의 혼합효소 Viscozyme L과 Celluclast 1.5 L를 이용하여 효소당화를 수행하였다. 50.4 g/l의총단당류의농도는, 120 g dw/l 꼬시래기 슬러리로부터 열산가수분해와효소당화에 의해 총 탄수화물 60 g/l의 전환율 84.2%를 나타내었다. 꼬시래기 가수분해산물은 분리당화발효(SHF)로 에탄올 생산을 위한 기질로 사용하였다. 고농도 galactose로 순치한 Candida lusitaniae ATCC42720에 의한 에탄올 생산은 0.43의 에탄올 수율(YEtOH)인 22.0 g/l를 생산하였다. 특정 당에 순치한 효모는 혼합당의 흡수에 유용하며, 그 결과 해조류가수분해산물배지로부터 높은 에탄올 수율을 나타내었다.
The seaweed, Gracilaria verrucosa, was fermented to produce bioethanol. Optimal pretreatment conditions were determined to be 12% (w/v) seaweed slurry and 270 mM sulfuric acid at 121℃ for 60 min. After thermal acid hydrolysis, enzymatic saccharification was carried out with 16 U/ml of mixed e...
The seaweed, Gracilaria verrucosa, was fermented to produce bioethanol. Optimal pretreatment conditions were determined to be 12% (w/v) seaweed slurry and 270 mM sulfuric acid at 121℃ for 60 min. After thermal acid hydrolysis, enzymatic saccharification was carried out with 16 U/ml of mixed enzymes using Viscozyme L and Celluclast 1.5 L to G. verrucosa hydrolysates. A total monosaccharide concentration of 50.4 g/l, representing 84.2% conversion of 60 g/l total carbohydrate from 120 g dw/l G. verrucosa slurry was obtained by thermal acid hydrolysis and enzymatic saccharification. G. verrucosa hydrolysate was used as the substrate for ethanol production by separate hydrolysis and fermentation (SHF). Ethanol production by Candida lusitaniae ATCC 42720 acclimated to high-galactose concentrations was 22.0 g/l with ethanol yield (YEtOH) of 0.43. Acclimated yeast to high concentrations of specific sugar could utilize mixed sugars, resulting in higher ethanol yields in the seaweed hydrolysates medium.
The seaweed, Gracilaria verrucosa, was fermented to produce bioethanol. Optimal pretreatment conditions were determined to be 12% (w/v) seaweed slurry and 270 mM sulfuric acid at 121℃ for 60 min. After thermal acid hydrolysis, enzymatic saccharification was carried out with 16 U/ml of mixed enzymes using Viscozyme L and Celluclast 1.5 L to G. verrucosa hydrolysates. A total monosaccharide concentration of 50.4 g/l, representing 84.2% conversion of 60 g/l total carbohydrate from 120 g dw/l G. verrucosa slurry was obtained by thermal acid hydrolysis and enzymatic saccharification. G. verrucosa hydrolysate was used as the substrate for ethanol production by separate hydrolysis and fermentation (SHF). Ethanol production by Candida lusitaniae ATCC 42720 acclimated to high-galactose concentrations was 22.0 g/l with ethanol yield (YEtOH) of 0.43. Acclimated yeast to high concentrations of specific sugar could utilize mixed sugars, resulting in higher ethanol yields in the seaweed hydrolysates medium.
lusitaniae displays a fast initial ethanol production rate and attains high ethanol conversions [15]. The objective of this study was to optimize the pretreatment conditions, such as thermal acid hydrolysis, enzymatic saccharification and ethanol fermentation for the red seaweed G. verrucosa.
대상 데이터
The culture of C. lusitaniae ATCC 42720, purchased from the American Type Culture Collection (ATCC), was grown in YPD medium containing 10 g/l yeast extract, 20 g/l peptone and 20 g/l glucose. The culture was incubated with agitation at 150 rpm for 24 h at 30℃.
성능/효과
In conclusion, the optimal pretreatment conditions of seaweed G. verrucosa were determined to be 12% of slurry and 270 mM of sulfuric acid at 121℃ for 60 minutes.
[12] reported high salt concentrations resulted in the rapid inhibition of cell growth and ethanol fermentation. Therefore, 12% (w/v) seaweed content with Eps of 84.2% was selected as the optimal seaweed slurry content for ethanol production.
The composition of G. verrucosa was analyzed by the AOAC method which revealed 66.9% carbohydrate, 10.6% crude fiber, 9.5% crude protein, 0.6% crude lipid, and 12.4% crude ash among other minor components. The weight ratio of galactose to AHG in the agar content was reported to be 0.
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