首页> 外文期刊>Annals of Microbiology >Ethanol production from Kinnow mandarin (Citrus reticulata) peels via simultaneous saccharification and fermentation using crude enzyme produced by Aspergillus oryzae and the thermotolerant Pichia kudriavzevii strain
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Ethanol production from Kinnow mandarin (Citrus reticulata) peels via simultaneous saccharification and fermentation using crude enzyme produced by Aspergillus oryzae and the thermotolerant Pichia kudriavzevii strain

机译:使用米曲霉和耐热毕赤酵母菌株生产的粗酶,通过同时糖化和发酵,从Kinnow柑桔(Citrus reticulata)生产乙醇。

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The aim of this study was to assess the potential of using the crude filtrate extract (CFE) produced by a newly isolated strain of Aspergillus oryzae and fermentation with a novel thermotolerant strain of Pichia kudriavzevii for the production of ethanol from kinnow peel waste (KP) via simultaneous saccharification and fermentation (SSF). High-performance liquid chromatography determination showed that pre-hydrolysis of KP with CFE at 3 cellulase filter paper units/g dry substrate (FPU/g-ds) at 50°C resulted in 24.87 ± 0.75 g l-1 glucose, 21.98 ± 0.53 g l-1 fructose, 10.86 ± 0.34 g l-1 sucrose and 6.56 ± 0.29 g l-1 galacturonic acid (GA) along with insignificant amounts of arabinose, galactose and xylose. Simultaneous saccharification and fermentation of hydrothermally pretreated KP at a substrate concentration of 15% (w v-1) was conducted in a 2.5-l laboratory fermentor with P. kudriavzevii at 40°C after a 3-h pre-hydrolysis. Oligosaccharides were not produced during the SSF process. Ethanol production leveled off after 12 h, resulting in an ethanol concentration and productivity of 33.87 g l-1 and 2.82 g l-1 h-1, respectively. These results demonstrate the potentiality of SSF using crude enzymes and P. kudriavzevii for the scale-up production of ethanol from KP.
机译:这项研究的目的是评估使用由新分离的米曲霉菌株生产的粗滤液提取物(CFE)并与新型耐热菌株毕赤酵母(Pichia kudriavzevii)发酵以从Kinnow果皮废料(KP)生产乙醇的潜力通过同时糖化和发酵(SSF)。高效液相色谱法测定表明,在50°C下3纤维素酶滤纸单位/ g干底物(FPU / g-ds)在300°C下用CFE对KP进行预水解会产生24.87±0.75 gl -1 葡萄糖,21.98±0.53 gl -1 果糖,10.86±0.34 gl -1 蔗糖和6.56±0.29 gl -1 半乳糖醛酸(GA )以及少量的阿拉伯糖,半乳糖和木糖。在2.5升实验室发酵罐中,在40℃下将古德里氏疟原虫在2.5升实验室发酵罐中进行水热预处理的KP的同时糖化和发酵,底物浓度为15%(wv -1 ),经过3小时预发酵-水解。 SSF过程中未产生寡糖。 12小时后乙醇生产趋于平稳,乙醇浓度和生产率分别为33.87 gl -1 和2.82 gl -1 h -1 ,分别。这些结果证明了使用粗酶和库氏假单胞菌(P. kudriavzevii)进行SSF的潜力,从KP大规模生产乙醇。

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