Kondo Tetsuo, Nojiri Masanobu, Hishikawa Yukako, Togawa Eiji, Romanovicz Dwight, Brown R Malcolm
Forestry and Forest Products Research Institute, P.O. Box 16, Tsukuba Norin, Ibaraki 305-8687, Japan.
Proc Natl Acad Sci U S A. 2002 Oct 29;99(22):14008-13. doi: 10.1073/pnas.212238399. Epub 2002 Oct 10.
Biodirected epitaxial nanodeposition of polymers was achieved on a template with an oriented molecular surface. Acetobacter xylinum synthesized a ribbon of cellulose I microfibrils onto a fixed, nematic ordered substrate of glucan chains with unique surface characteristics. The substrate directed the orientation of the motion due to the inverse force of the secretion during biosynthesis, and the microfibrils were aligned along the orientation of the molecular template. Using real-time video analysis, the patterns and rates of deposition were elucidated. Field emission scanning electron microscopy revealed that a strong molecular interaction allowed for the deposition of nascent biosynthesized 3.5-nm cellulose microfibrils with inter-microfibrillar spacings of 7-8 nm on the surface of the template. The cellulose was deposited parallel to the molecular orientation of the template. Directed cellulose synthesis and ordered movement of cells were observed only by using a nematic ordered substrate made from cellulose, and not from ordered crystalline cellulose substrates or ordered cellulose-related synthetic polymers such as polyvinyl alcohol. This unique relationship between directed biosynthesis and the ordered fabrication from the nano to the micro scales could lead to new methodologies for the design of functional materials with desired nanostructures.
在具有定向分子表面的模板上实现了聚合物的生物定向外延纳米沉积。木醋杆菌在具有独特表面特性的葡聚糖链的固定向列有序底物上合成了纤维素I微纤丝带。由于生物合成过程中分泌的反向力,底物引导了运动的方向,微纤丝沿着分子模板的方向排列。通过实时视频分析,阐明了沉积的模式和速率。场发射扫描电子显微镜显示,强烈的分子相互作用使得新生的生物合成3.5纳米纤维素微纤丝能够以7-8纳米的微纤丝间距沉积在模板表面。纤维素平行于模板的分子方向沉积。仅通过使用由纤维素制成的向列有序底物,而非有序结晶纤维素底物或有序纤维素相关合成聚合物(如聚乙烯醇),观察到了定向纤维素合成和细胞的有序运动。这种从纳米到微米尺度的定向生物合成与有序制造之间的独特关系可能会带来设计具有所需纳米结构的功能材料的新方法。