Jovetica S, Beeftink H H., Tramper J, Marinelli F
Biosearch Italia S.p.A., Via R. Lepetit 34, 21040 (VA), Gerenzano, Italy
Enzyme Microb Technol. 2001 Apr 5;28(6):510-514. doi: 10.1016/s0141-0229(01)00292-7.
Effective diffusion coefficients (D(e)) of antibiotic A40926 and its deacylated derivative were determined in Ca-alginate (2% wt/wt) and kappa-carrageenan (2.6% wt/wt) gel beads with or without immobilized Actinoplanes teichomyceticus cells and/or soybean meal (SBM). The method used was based on transient concentration changes in a well-stirred antibiotic solution in which gel beads, initially free of solute, were suspended. Unsteady-state diffusion in a sphere was applied and D(e) determined from the best fit of experimental data. A40926 showed markedly different diffusion characteristics than its deacylated derivative. Diffusivity of deacyl-A40926 in alginate or carrageenan gel beads was six to seven times that of A40926. Large differences in partition coefficients (Kp) were also found. In case of beads without additions, A40926, in contrast to deacyl-A40926, strongly partitioned to the liquid phase. Introduction of SBM and/or mycelium in the gel beads decreased the effective diffusivity of deacyl-A40926, but increased its partitioning to the solid phase. Our findings indicate that a relatively moderate structural change of a lipoglycopeptide molecule could lead to a major change in its diffusion/partition characteristics.
在含有或不含有固定化的栖土放线菌细胞和/或豆粕(SBM)的海藻酸钙(2%重量/重量)和κ-卡拉胶(2.6%重量/重量)凝胶珠中,测定了抗生素A40926及其脱酰基衍生物的有效扩散系数(D(e))。所采用的方法基于在一个充分搅拌的抗生素溶液中瞬时浓度的变化,在该溶液中悬浮着最初不含溶质的凝胶珠。应用了球体中的非稳态扩散,并根据实验数据的最佳拟合确定了D(e)。A40926与其脱酰基衍生物表现出明显不同的扩散特性。脱酰基-A40926在海藻酸盐或卡拉胶凝胶珠中的扩散率是A40926的六到七倍。还发现了分配系数(Kp)的巨大差异。在未添加物质的珠子的情况下,与脱酰基-A40926相反,A40926强烈分配到液相中。在凝胶珠中引入SBM和/或菌丝体降低了脱酰基-A40926的有效扩散率,但增加了其向固相的分配。我们的研究结果表明,脂糖肽分子相对适度的结构变化可能导致其扩散/分配特性发生重大变化。