摘要
We prepared the penta-N-acetyl-chitopentaose 2 by using recombinant Escherichia coli ( E. coli) strains harboring the nodC gene ( encoding chitooligosaccharide synthase) from Azorhizobium caulinodans. The deacetylase NodB removed the N-acetyl moiety from the nonreducing terminus of 2 to give tetra-N-acetyl-chitopentaose 3. N-Acylation of 3 with stearyl chloride was performed in DMF containing water and provided the corresponding lipo-chitopentaose nodulation factor 4.
- 出版日期2007
- 单位重庆师范大学