Korany Shereen M, El-Hendawy Hoda H, Sonbol Hana, Hamada Marwa A
Department of Biology, College of Science, Princess Nourah Bint Abdulrahman University, 84428 Riyadh, Saudi Arabia.
Botany and Microbiology Department, Faculty of Science, Helwan University, Helwan, 11795 Cairo, Egypt.
Saudi J Biol Sci. 2021 Nov;28(11):6679-6689. doi: 10.1016/j.sjbs.2021.08.008. Epub 2021 Aug 9.
Microbial levan has great potential as a functional biopolymer in different fields including foods, feeds, cosmetics, and the pharmaceutical and chemical industries. In this study, a good levan producer bacterial strain of strain ES, isolated from soil in Egypt in a previous study, was used. Levan production by this strain was optimized using Plackett-Burman experimental design (PBD) to screen the critical factors of several process variables and Centered Central Composite Design (CCD) was applied for further estimation of the relationship between the variables and the response as well as optimization of the levels. Plackett-Burman (P-B) design showed a p-value 0.0144 less than 0.05 indicated the significance of the model. Sucrose, potassium dihydrogen phosphate, yeast extract and pH value showed the most significant effect on levan concentration at the values of 89.17, 65.83, 24.17, and 15.83, respectively. The purified levan polymer was characterized using different Physico-chemical methods such as Fourier Transform Infrared Spectrometer (FTIR), Nuclear magnetic resonance (NMR), and High-Performance Liquid Chromatography (HPLC) to determine the main composition and functional groups in the obtained polymer. HPLC results indicated that the polymer purification increased the percentage of fructose residue from 75 up to 89. Furthermore, H and C NMR spectroscopy analysis showed great matching between the obtained signal for our polymer with that reported in other peoples work. The obtained levan polymer exhibited cytotoxic activity against Human epidermoid Skin carcinoma and Hepatocellular carcinoma with IC50 of 469 and 222.7 µg/ml, respectively. Antioxidant activity was determined using DPPH assay and the percentage of inhibition at 1000 µg/ml was found to be <50 (13.89 ± 1.07) with IC50 of (24.42 ± 0.87).
微生物果聚糖作为一种功能性生物聚合物,在食品、饲料、化妆品以及制药和化工等不同领域具有巨大潜力。在本研究中,使用了先前研究中从埃及土壤分离出的优良果聚糖生产菌株ES。通过Plackett-Burman实验设计(PBD)对该菌株的果聚糖生产进行优化,以筛选多个工艺变量的关键因素,并应用中心复合设计(CCD)进一步估计变量与响应之间的关系以及水平优化。Plackett-Burman(P-B)设计显示p值0.0144小于0.05,表明模型具有显著性。蔗糖、磷酸二氢钾、酵母提取物和pH值对果聚糖浓度的影响最为显著,其值分别为89.17、65.83、24.17和15.83。使用傅里叶变换红外光谱仪(FTIR)、核磁共振(NMR)和高效液相色谱(HPLC)等不同的物理化学方法对纯化的果聚糖聚合物进行表征,以确定所得聚合物中的主要成分和官能团。HPLC结果表明,聚合物纯化使果糖残基的百分比从75%提高到了89%。此外,H和C NMR光谱分析表明,我们所得聚合物的信号与其他人工作中报道的信号高度匹配。所得的果聚糖聚合物对人表皮样皮肤癌和肝癌表现出细胞毒性活性,IC50分别为469和222.7μg/ml。使用DPPH法测定抗氧化活性,发现在1000μg/ml时的抑制百分比<50(13.89±1.07),IC50为(24.42±0.87)。