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Unusual, pH-induced, self-assembly of sophorolipid biosurfactants

机译:异常的,pH诱导的槐糖脂类生物表面活性剂的自组装

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An increasing need exists for simple, bioderived, nontoxic, and up-scalable compounds with stimuli-responsive properties. Acidic sophorolipids (SL) are glucose-based biosurfactants derived from the yeast broth of Candida bombicola (teleomorph: Starmerella bombicola). The specific design of this molecule, a sophorose head with a free end-COOH group at the end of the alkyl chain, makes it a potentially interesting pH-responsive compound. We have specifically investigated this assumption using a combination of small angle neutron scattering (SANS), transmission electron microscopy under cryogenic conditions (Cryo-TEM), and nuclear magnetic resonance (NMR) techniques and found a strong dependence of SL self-assembly on the degree of ionization, α, of the COOH group at concentration values as low as 5 and 0.5 wt %. At least three regimes can be identified where the supramolecular behavior of SL is unexpectedly different: (1) at low α values, self-assembly is driven by concentration, C, and micelles are mainly identified as nonionic objects whose curvature decreases (sphere-to-rod) with C; (2) at mid α values, the formation of COO ~- groups introduces negative charges at the micellar surface inducing an increase in curvature (rod-to-sphere transition). Repulsive electrostatic long-range interactions appear at this stage. In both regimes 1 and 2, the cross-section radius of the micelles is below 25 ?. This behavior is concentration independent. (3) At α = 1, individual micelles seem to favor the formation of large netlike tubular aggregates whose size is above 100 nm. Such a complex behavior is very unique as it is generally not observed for common alkyl-based surfactants in concentration ranges below 5-10 wt %.
机译:对具有刺激响应特性的简单的,生物来源的,无毒的和可放大的化合物的需求日益增长。酸性槐糖脂(SL)是基于葡萄糖的生物表面活性剂,来源于念珠菌念珠菌(teleomorph:Starmerella bombicola)。该分子的特殊设计,即在烷基链末端带有一个游离COOH端基的槐糖头,使其成为一种可能令人感兴趣的pH响应化合物。我们通过结合小角度中子散射(SANS),低温条件下的透射电子显微镜(Cryo-TEM)和核磁共振(NMR)技术,专门研究了这一假设,并发现SL自组装强烈依赖于浓度值低至5和0.5 wt%时,COOH基团的电离度α。至少可以识别出SL的超分子行为出乎意料地不同的三种状态:(1)在低α值下,自组装受浓度驱动,C且胶束主要被识别为曲率下降的非离子物体(球到-rod)和C; (2)在中间α值处,COO〜-的形成会在胶束表面引入负电荷,从而导致曲率增加(杆-球过渡)。在此阶段出现排斥性静电远程相互作用。在方案1和方案2中,胶束的横截面半径均小于25?。此行为与浓度无关。 (3)在α= 1时,单个胶束似乎倾向于形成尺寸大于100 nm的大型网状管状聚集体。这种复杂的行为非常独特,因为通常在浓度范围低于5-10 wt%的普通烷基烷基表面活性剂中观察不到。

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