首页> 外文期刊>Research Letters in Biochemistry >Effect of pH, Temperature, and Chemicals on the Endoglucanases and β-Glucosidases from the Thermophilic Fungus Myceliophthora heterothallica F.2.1.4. Obtained by Solid-State and Submerged Cultivation
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Effect of pH, Temperature, and Chemicals on the Endoglucanases and β-Glucosidases from the Thermophilic Fungus Myceliophthora heterothallica F.2.1.4. Obtained by Solid-State and Submerged Cultivation

机译:pH,温度和化学物质对嗜热真菌Mythliophthora heterothallica F.2.1.4的内切葡聚糖酶和β-葡糖苷酶的影响。通过固态和深耕获得

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This work reports endoglucanase and beta-glucosidase production by the thermophilic fungus Myceliophthora heterothallica in solid-state (SSC) and submerged (SmC) cultivation. Wheat bran and sugarcane bagasse were used for SSC and cardboard for SmC. Highest endoglucanase production in SSC occurred after 192 hours 1,170.6 ± 0.8 U/g, and in SmC after 168 hours 2,642 ± 561 U/g. The endoglucanases and beta-glucosidases produced by both cultivation systems showed slight differences concerning their optimal pH and temperature. The number of endoglucanases was also different six isoforms in SSC and ten in SmC. Endoglucanase activity remained above 50% after incubation between pH 3.0 and 9.0 for 24 h for both cultivation systems. The effect of several chemicals displayed variation between SSC and SmC isoenzymes. Manganese activated the enzymes from SmC but inhibited those from SSC. For β-glucosidases, maximum production on SmC was 244 ± 48 U/g after 168 hours using cardboard as carbon source. In SSC maximum production reached 10.9 ± 0.3 U/g after 240 h with 1  1 wheat bran and sugarcane bagasse. Manganese exerted a significant activation on SSC β-glucosidases, and glucose inhibited the enzymes from both cultivation systems. FeCl3 exerted the strongest inhibition for endoglucanases and β-glucosidases.
机译:这项工作报告了嗜热真菌异丝霉在固态(SSC)和水下(SmC)培养中产生的内切葡聚糖酶和β-葡萄糖苷酶。麦麸和甘蔗渣用于SSC,纸板用于SmC。 SSC中最高的内切葡聚糖酶产量在192小时后为1,170.6±0.8 / U / g,SmC在168小时后达到了2,642±561 U / g。两种培养系统产生的内切葡聚糖酶和β-葡萄糖苷酶在最适pH和温度方面均存在细微差异。内切葡聚糖酶的数目在SSC中也有6种亚型,在SmC中有10种。在两种培养系统中,在3.0至9.0的pH下孵育24小时后,内切葡聚糖酶的活性均保持在50%以上。几种化学药品的作用显示出SSC和SmC同工酶之间的差异。锰激活了SmC中的酶,但抑制了SSC中的酶。对于β-葡萄糖苷酶,使用纸板作为碳源,在168小时后,SmC的最大产量为244±48 U / g。在SSC中,用1×1麦麸和甘蔗渣处理240 h后,最高产量达到10.9±0.3 U / g。锰对SSCβ-葡萄糖苷酶具有显着的活化作用,而葡萄糖抑制了两种培养系统中的酶。 FeCl3对内切葡聚糖酶和β-葡萄糖苷酶的抑制作用最强。

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