Suppr超能文献

自组装单分子层与木质纤维素底物之间纳米级粘附力的异质性和特异性:化学力显微镜研究

Heterogeneity and Specificity of Nanoscale Adhesion Forces Measured between Self-Assembled Monolayers and Lignocellulosic Substrates: A Chemical Force Microscopy Study.

作者信息

Arslan Baran, Ju Xiaohui, Zhang Xiao, Abu-Lail Nehal I

机构信息

Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University , Pullman, Washington 99164-6515, United States.

Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Bioproducts' Science and Engineering Laboratory, Washington State University , Richland, Washington 99354-1670, United States.

出版信息

Langmuir. 2015 Sep 22;31(37):10233-45. doi: 10.1021/acs.langmuir.5b02633. Epub 2015 Sep 4.

Abstract

Lack of fundamental understanding of cellulase interactions with different plant cell wall components during cellulose saccharification hinders progress toward achieving an economic production of biofuels from renewable plant biomass. Here, chemical force microscopy (CFM) was utilized to quantify the interactions between two surfaces that model either hydrophilic or hydrophobic functional groups of cellulases and a set of lignocellulosic substrates prepared through Kraft, sulfite, or organosolv pulping with defined chemical composition. The measured forces were then decoupled into specific and nonspecific components using the Poisson statistical approach. Heterogeneities in the distributions of forces as a function of the pretreatment method were mapped. Our results showed that hydrophobic domains and chemical moieties involved in hydrogen bonding and polar interactions were homogeneously distributed on all substrates but with distribution densities that varied with the type of the pretreatment method used to prepare substrates. In addition, we showed that increasing surface lignin coverage increased the heterogeneity of the substrates. When forces were decoupled, our results indicated that xylan reduced the strength of hydrogen bonding between the hydrophilic model surface and substrates. Permanent dipole-dipole interactions dominated the adhesion of the hydrophilic model surface to lignosulfonates, whereas hydrophobic interactions facilitated the adhesion of the hydrophobic model surface to Kraft lignin. We further showed that the structure of lignin determines the type of forces that dominate lignocellulosic interactions with other surfaces. Our findings suggest that nonproductive binding of cellulases to lignocellulosic biomass can be reduced by altering the hydrophobicity and/or chemical moieties involved in the polar interactions and by utilizing organosolv as a pretreatment method.

摘要

在纤维素糖化过程中,缺乏对纤维素酶与不同植物细胞壁成分相互作用的基本了解,阻碍了从可再生植物生物质中实现生物燃料经济生产的进程。在此,利用化学力显微镜(CFM)来量化模拟纤维素酶亲水性或疏水性官能团的两个表面与一组通过硫酸盐法、亚硫酸盐法或有机溶剂法制浆且具有确定化学成分的木质纤维素底物之间的相互作用。然后,使用泊松统计方法将测得的力解耦为特定和非特定成分。绘制了作为预处理方法函数的力分布的不均匀性。我们的结果表明,参与氢键和极性相互作用的疏水区域和化学基团在所有底物上均均匀分布,但分布密度随用于制备底物的预处理方法类型而变化。此外,我们表明增加表面木质素覆盖率会增加底物的不均匀性。当力被解耦时,我们的结果表明木聚糖降低了亲水性模型表面与底物之间氢键的强度。永久偶极 - 偶极相互作用主导了亲水性模型表面与木质素磺酸盐的粘附,而疏水相互作用促进了疏水性模型表面与硫酸盐木质素的粘附。我们进一步表明,木质素的结构决定了主导木质纤维素与其他表面相互作用的力的类型。我们的研究结果表明,通过改变参与极性相互作用的疏水性和/或化学基团以及使用有机溶剂法作为预处理方法,可以减少纤维素酶与木质纤维素生物质的非生产性结合。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验