Bou-Sarkis Abdo, Paul Etienne, Girbal-Neuhauser Elisabeth, Derlon Nicolas, Bessiere Yolaine
LBAE, Laboratoire de Biotechnologies Agroalimentaire et Environnementale (UPS, URU 4565), Université de Toulouse, Institut Universitaire de Technologie, 24 rue d'Embaquès, 32000 Auch, France.
TBI, Université de Toulouse, CNRS, INRAE, INSA, 135 avenue de Rangueil, CEDEX 04, 31077 Toulouse, France.
Gels. 2023 Feb 16;9(2):157. doi: 10.3390/gels9020157.
The valorization of biological aggregates through the extraction of hydrogel-forming polymers can enhance the economics and sustainability of various processes in which bacteria are involved in organic waste transformation, such as wastewater treatment. Achieving these goals requires the development of a method capable of detecting the presence of gel-forming polymers in complex mixtures containing biopolymers that are most often unknown and uncharacterized. A miniaturized screening method capable of detecting gelation via ionic crosslinking using only 1 to 3 mg of the tested samples (commercial molecules or extracellular polymeric substances, EPSs) is proposed. The method consists of calculating a percentage of reactivity (%R) through UV-vis spectra and determining the percentage of gel volume (%Vg) formed after the addition of calcium. Both factors were combined to give a gelling factor (GF), and the test was applied to pure commercial molecules (BSA, DNA, alginate (ALV), and a mixture of them), allowing the classification of the following solutions according to their gel-forming capacity: GF > GF > GF > GF > GF > GF > GF. As a relevant tool for screening hydrogel-forming solutions, the method was applied to the EPS extracted from aerobic granular sludge. The EPS (0.5% /) had a GF of 0.16 ± 0.03, equivalent to approximately half of the GF of ALV (0.38 ± 0.02 at 0.5% /). The developed test pushes the limits of the existing gel-detection techniques because it allows for quicker, less consuming, and more informative gelation detection through the use of simple methods that do not require sophisticated equipment.
通过提取形成水凝胶的聚合物来实现生物聚集体的增值,可以提高各种涉及细菌参与有机废物转化过程(如废水处理)的经济性和可持续性。要实现这些目标,需要开发一种能够检测复杂混合物中形成凝胶的聚合物的方法,这些混合物中含有通常未知且未表征的生物聚合物。本文提出了一种仅使用1至3毫克测试样品(商业分子或细胞外聚合物,EPS)就能通过离子交联检测凝胶化的小型化筛选方法。该方法包括通过紫外可见光谱计算反应性百分比(%R),并确定添加钙后形成的凝胶体积百分比(%Vg)。将这两个因素结合起来得到凝胶化因子(GF),并将该测试应用于纯商业分子(牛血清白蛋白、DNA、海藻酸盐(ALV)及其混合物),从而根据其凝胶形成能力对以下溶液进行分类:GF>GF>GF>GF>GF>GF>GF。作为筛选形成水凝胶溶液的相关工具,该方法应用于从好氧颗粒污泥中提取的EPS。EPS(0.5%/)的GF为0.16±0.03,约为ALV(0.5%/时为0.38±0.02)的GF的一半。所开发的测试突破了现有凝胶检测技术的极限,因为它通过使用不需要复杂设备的简单方法,能够更快、更省力且更有信息地检测凝胶化。