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酶对不同纸浆精制的影响。

Effects of enzymes on the refining of different pulps.

机构信息

Institute of Environmental Biotechnology, University of Natural Resources and Life Sciences Vienna, Konrad-Lorenz-Strasse 20, 3430, Tulln an der Donau, Austria.

Graz University of Technology, Institute of Paper, Pulp and Fiber Technology, Inffeldgasse 23, Graz, 8010, Austria.

出版信息

J Biotechnol. 2020 Aug 20;320:1-10. doi: 10.1016/j.jbiotec.2020.06.006. Epub 2020 Jun 14.

Abstract

Comparative studies of the effects of two commercial enzyme formulations on fiber refining were conducted. Extensive basic characterisation of the enzymes involved, assessment of their hydrolytic activities on different model substrates as well as on different pulps (softwood sulfate, softwood sulfite, hardwood sulfate) were evaluated. Both enzyme formulations showed endoglucanase as well as some xylanase and β-glucosidase activity. In addition, Enzyme A reached a CMC end viscosity of 19.5 mPa compared to 11.1 mPa for Enzyme B. Reducing sugar release almost doubled from 695 μmol mL for hardwood sulfate pulp to 1300 μmol mL for softwood sulfite pulp with Enzyme B under the same conditions. Enzyme A increased the degree of refining even under non-ideal conditions from 23 °SR to up to 50 °SR. Further characterization of hand sheets, made from enzyme pre-treated and refined cellulose fibers with Enzyme A and B, showed that Enzyme A had the best effects leading to hand sheets with increased tensile strength and low air permeability. In summary, the increase in the degree of refining seen for Enzyme A correlated to higher xylanase and β-glucosidase activity and lower endoglucanase activity.

摘要

进行了两种商业酶制剂对纤维精炼效果的比较研究。对涉及的酶进行了广泛的基础特性分析,评估了它们在不同模型底物以及不同纸浆(软木硫酸盐、软木亚硫酸盐、硬木硫酸盐)上的水解活性。两种酶制剂均显示出内切葡聚糖酶以及一些木聚糖酶和β-葡萄糖苷酶活性。此外,酶 A 的 CMC 末端黏度达到 19.5 mPa,而酶 B 为 11.1 mPa。在相同条件下,用酶 B 处理硬木硫酸盐纸浆时,还原糖释放量几乎翻了一番,从 695 μmol·mL 增加到 1300 μmol·mL。即使在不理想的条件下,酶 A 也能将打浆度从 23°SR 提高到 50°SR。用酶 A 和 B 预处理和精炼的纤维素纤维制成手抄片进一步进行特性分析表明,酶 A 的效果最佳,导致手抄片的拉伸强度增加,空气渗透性降低。总之,酶 A 的打浆度提高与更高的木聚糖酶和β-葡萄糖苷酶活性以及更低的内切葡聚糖酶活性相关。

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