Department of Bioscience, Graduate School of Science and Technology, Shizuoka University, Ohya 836, Suruga Ward, Shizuoka 422-8529, Japan.
Carbohydr Res. 2012 Jan 10;347(1):16-22. doi: 10.1016/j.carres.2011.09.025. Epub 2011 Sep 29.
The enzymatic synthesis of an α-chitin-like substance via a non-biosynthetic pathway has been achieved by transglycosylation in an aqueous system of the corresponding substrate, tri-N-acetylchitotriose [(GlcNAc)(3)] for lysozyme. A significant amount of water-insoluble product precipitated out from the reaction system. MALDI-TOFMS analysis showed that the resulting precipitate had a degree of polymerization (DP) of up to 15 from (GlcNAc)(3). Solid-state (13)C NMR analysis revealed that the resulting water-insoluble product is a chitin-like substance consisting of N-acetylglucosamine (GlcNAc) residues joined exclusively in a β-(1→4)-linked chain with stringent regio-/stereoselection. X-ray diffraction (XRD) measurement as well as (13)C NMR analysis showed that the crystal structure of synthetic product corresponds to α-chitin with a high degree of crystallinity. We propose that the multiple oligomers form an α-chitin-like substance as a result of self-assembly via oligomer-oligomer interaction when they precipitate.
通过在相应的酶切反应的水相体系中进行转糖苷反应,实现了通过非生物合成途径对一种类似α-壳聚糖物质的酶法合成。大量的不溶性产物从反应体系中沉淀出来。MALDI-TOFMS 分析表明,所得沉淀的聚合度(DP)高达 15。固态(13)C NMR 分析表明,所得不溶性产物是一种类似壳聚糖的物质,由 N-乙酰葡萄糖胺(GlcNAc)残基以严格的区域/立体选择性仅以β-(1→4)-连接链连接而成。X 射线衍射(XRD)测量和(13)C NMR 分析表明,合成产物的晶体结构与具有高结晶度的α-壳聚糖相对应。我们提出,当这些多聚物沉淀时,通过多聚物-多聚物相互作用自组装形成类似α-壳聚糖的物质。