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首页> 外文期刊>Biomass Conversion and Biorefinery >beta-Glucosidase production by Trichoderma reesei and Thermoascus aurantiacus by solid state cultivation and application of enzymatic cocktail for saccharification of sugarcane bagasse
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beta-Glucosidase production by Trichoderma reesei and Thermoascus aurantiacus by solid state cultivation and application of enzymatic cocktail for saccharification of sugarcane bagasse

机译:β-葡萄糖苷酶通过Trichoderma Reesei和Thermoascus Aurantiacus通过固态培养和酶促鸡尾酒用于糖甘油蔗糖糖化的培养和应用

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For degradation of sugarcane bagasse (SCB), several enzymes are needed but beta-glucosidase is rate limiting in cellulose hydrolysis. Since different microorganisms synthetize characteristic pool of enzymes, mixing extracts produced by different species may increase hydrolytic efficiency due to synergism between enzymes in cocktails. This paper reports the study of beta-glucosidase production in solid state cultivation (SSC) of two filamentous fungi, thermophilic Thermoascus aurantiacus and mesophilic Trichoderma reesei, and application of the enzymatic extracts on non-pretreated SCB saccharification. Enzyme extract obtained from the thermophilic fungus presented higher beta-glucosidase and FPU activities (1.8 U/mL and 10 FPU/mL) than the one from mesophilic (0.2 U/mL and 6 FPU/mL). Optimal SCB hydrolysis was achieved when applying enzymatic cocktail composed of equal volumes of both fungal extracts (3.6 FPU/g(SCB), filter paper units per gram SCB, 2.25 FPU/g(SCB) provided by extract from T. aurantiacus and 1.35 FPU/g(SCB) from T. reesei) at 65 degrees C. The hydrolysis yield applying the enzyme cocktail, 124 mg total reducing sugars (TRS) per g(SCB), was higher than any yield achieved when using the enzyme extracts separately (105 mg(TRS)/g(SCB) using 12.5 FPU per g(SCB) from T. aurantiacus at 65 degrees C; 79 mg(TRS)/g(SCB) using 7.5 FPU per g(SCB) from T. reesei at 45 degrees C). Therefore, the use of the cocktail (3.6 FPU/g(SCB)) at 65 degrees C released 18 and 57% more TRS respectively than when extracts from T. aurantiacus or from T. reesei were applied alone, respectively, even reducing enzyme load (FPU) by 70%, corroborating the synergistic effect when both extracts are used together.
机译:对于甘蔗甘蔗蛋白(SCB)的降解,需要几种酶但β-葡糖苷酶是纤维素水解的速率限制。由于不同的微生物合成特征酶池,因此通过不同物种产生的混合提取物可能增加由于鸡尾酒中酶之间的协同作用而增加的水解效率。本文报道了两种丝状真菌,嗜热嗜热嗜热菌,嗜热性培养物和嗜热性培养蛋白Reesei的β-葡萄糖苷酶生产的研究,以及在非预处理SCB糖化上的酶促提取物的应用。从嗜热真菌获得的酶提取物呈现比来自嗜苯胺(0.2u / ml和6fpu / ml)的β-葡糖苷酶和FPU活性(1.8u / ml和10fpu / ml)。当施用由T. aurantiacus和1.35 FPU的提取物提供的相同的真菌提取物(3.6fpu / g(SCB),每克SCB,2.25fpu / g(scb)组成的酶鸡尾酒时,实现了最佳的SCB水解。 / g(SCB)从T.Reesei)在65℃下,施用酶鸡尾酒的水解产量124mg总还原糖(TRS),较单独使用酶提取物时所达到的任何产率( 105mg(TRS)/ g(SCB)使用来自T. aurantiacus的12.5fpu / g(SCB),在65℃下,使用来自T.Reesei的79mg(TRS)/ g(SCB),从T. Reesei使用7.5 FPU 45℃)。因此,在65摄氏度中释放了鸡尾酒(3.6fpu / g(scb))分别比从T. aurantiacus或T.reesei的提取物体释放的18和57%的TRS,即使还原酶载荷(FPU)×70%,在两个提取物一起使用时证实了协同效应。

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