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利用芋头废料优化嗜酸乳杆菌培养及其生物活性评估。

Optimization of Lactobacillus acidophilus cultivation using taro waste and evaluation of its biological activity.

作者信息

Hsieh Shu-Chen, Liu Jui-Ming, Pua Xiao-Hui, Ting Yuwen, Hsu Ren-Jun, Cheng Kuan-Chen

机构信息

Graduate Institute of Food Science Technology, National Taiwan University, Taipei, 10617, Taiwan.

Division of Urology, Department of Surgery, Taoyuan General Hospital, Ministry of Health and Welfare, 1492 Chung-Shan Road, Taoyuan District, Taoyuan, 330, Taiwan.

出版信息

Appl Microbiol Biotechnol. 2016 Mar;100(6):2629-39. doi: 10.1007/s00253-015-7149-1. Epub 2015 Nov 17.

Abstract

In this study, taro waste (TW) was utilized for Lactobacillus acidophilus BCRC 14079 cultivation and the anti-tumor and immune-modulatory properties of heat-killed cells (HKCs), cytoplasmic fraction (CF), and exopolysaccharide (EPS) were evaluated. The optimum liquefaction enzyme dosage, temperature, and time determined by Box-Behnken design response surface methodology (BBD-RSM) were 9 mL/L of α-amylase, 79.2 °C, and 5 h of reaction, respectively. The optimum temperature and reaction time for saccharification were determined as 60 °C and 3 h. The optimum medium, CGMY1 medium, constitutes of TW hydrolysate containing 37 g/L of glucose, 25 g/L of corn gluten meal (CGM), and 1 g/L of yeast extract (YE). Results of MTT assay showed that HKCs and EPS from CGM medium exhibited the highest anti-proliferative in HT-29 (IC50 of HKCs, 467.25 μg/mL; EPS, 716.10 μg/mL) and in Caco-2 cells (IC50 of EPS, 741.60 μg/mL). Luciferase-based NF-ΚB and COX-2 systems indicated HKCs from CGM medium stimulated the highest expression of luciferin in both systems. The luciferase activities by using 100 and 500 μg/mL of HKCs from CGM were 24.30- and 45.83-fold in NF-ΚB system and 11.54- and 4.93-fold in COX-2 system higher than the control. In conclusion, this study demonstrated the potential of TW medium for L. acidophilus cultivation and the production of non-viable probiotics with enhanced biological activities.

摘要

在本研究中,芋头废料(TW)被用于嗜酸乳杆菌BCRC 14079的培养,并评估了热灭活细胞(HKCs)、细胞质组分(CF)和胞外多糖(EPS)的抗肿瘤和免疫调节特性。通过Box-Behnken设计响应面法(BBD-RSM)确定的最佳液化酶用量、温度和时间分别为9 mL/L的α-淀粉酶、79.2℃和5小时的反应时间。糖化的最佳温度和反应时间分别确定为60℃和3小时。最佳培养基CGMY1培养基由含有37 g/L葡萄糖、25 g/L玉米蛋白粉(CGM)和1 g/L酵母提取物(YE)的TW水解产物组成。MTT分析结果表明,来自CGM培养基的HKCs和EPS在HT-29细胞(HKCs的IC50为467.25 μg/mL;EPS为716.10 μg/mL)和Caco-2细胞(EPS的IC50为741.60 μg/mL)中表现出最高的抗增殖活性。基于荧光素酶的NF-ΚB和COX-2系统表明,来自CGM培养基的HKCs在两个系统中刺激荧光素的表达最高。在NF-ΚB系统中,使用100和500 μg/mL来自CGM的HKCs时,荧光素酶活性分别比对照高24.30倍和45.83倍;在COX-2系统中分别高11.54倍和4.93倍。总之,本研究证明了TW培养基用于嗜酸乳杆菌培养以及生产具有增强生物活性的无活性益生菌的潜力。

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