Chorfa Nasima, Nlandu Hervé, Belkacemi Khaled, Hamoudi Safia
Department of Soil Sciences and Agri-Food Engineering, Centre in Green Chemistry and Catalysis, Laval University, Quebec City, QC G1V 0A6, Canada.
Polymers (Basel). 2022 May 16;14(10):2027. doi: 10.3390/polym14102027.
In this work, a valorization of the starch stemming from downgraded potatoes was approached through the preparation of starch nanoparticles using different physical methods, namely liquid and supercritical carbon dioxide, high energy ball milling (HEBM), and ultrasonication on the one hand and enzymatic hydrolysis on the other hand. Starch nanoparticles are beneficial as a reinforcement in food packaging technology as they enhance the mechanical and water vapor resistance of polymers. Also, starch nanoparticles are appropriate for medical applications as carriers for the delivery of bioactive or therapeutic agents. The obtained materials were characterized using X-ray diffraction as well as scanning and transmission electron microscopies (SEM and TEM), whereas the hydrolysates were analyzed using size exclusion chromatography coupled with pulsed amperometric detection (SEC-PAD). The acquired results revealed that the physical modification methods led to moderate alterations of the potato starch granules' size and crystallinity. However, enzymatic hydrolysis conducted using Pullulanase enzyme followed by nanoprecipitation of the hydrolysates allowed us to obtain very tiny starch nanoparticles sized between 20 and 50 nm, much smaller than the native starch granules, which have an average size of 10 μm. The effects of enzyme concentration, temperature, and reaction medium pH on the extent of hydrolysis in terms of the polymer carbohydrates' fractions were investigated. The most promising results were obtained with a Pullulanase enzyme concentration of 160 npun/g of starch, at a temperature of 60 °C in a pH 4 phosphate buffer solution resulting in the production of hydrolysates containing starch polymers with low molecular weights corresponding mainly to P-10, P-5, and fractions with molecular weights lower than P-5 Pullulan standards.
在这项工作中,一方面通过使用不同的物理方法,即液体和超临界二氧化碳、高能球磨(HEBM)和超声处理,另一方面通过酶促水解,对来自降级土豆的淀粉进行增值处理。淀粉纳米颗粒作为食品包装技术中的增强剂是有益的,因为它们增强了聚合物的机械性能和耐水蒸气性。此外,淀粉纳米颗粒作为生物活性或治疗剂递送的载体适用于医学应用。使用X射线衍射以及扫描和透射电子显微镜(SEM和TEM)对所得材料进行表征,而水解产物则使用尺寸排阻色谱结合脉冲安培检测(SEC-PAD)进行分析。获得的结果表明,物理改性方法导致马铃薯淀粉颗粒的尺寸和结晶度发生适度变化。然而,使用普鲁兰酶进行酶促水解,然后对水解产物进行纳米沉淀,使我们能够获得尺寸在20至50纳米之间的非常微小的淀粉纳米颗粒,比平均尺寸为10微米的天然淀粉颗粒小得多。研究了酶浓度、温度和反应介质pH对聚合物碳水化合物部分水解程度的影响。在pH 4的磷酸盐缓冲溶液中,温度为60°C,普鲁兰酶浓度为160 npun/g淀粉时,获得了最有希望的结果,产生了主要含有对应于P-10、P-5以及分子量低于P-5普鲁兰标准的低分子量淀粉聚合物的水解产物。