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采用固定化细胞发酵后,通过多次结晶作为一种从发酵液中高效回收琥珀酸的潜在策略。

Multiple crystallization as a potential strategy for efficient recovery of succinic acid following fermentation with immobilized cells.

机构信息

Research Centre for Sustainable Process Technology (CESPRO), Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia (UKM), 43600, Bangi, Selangor, Malaysia.

Department of Chemical and Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia (UKM), 43600, Bangi, Selangor, Malaysia.

出版信息

Bioprocess Biosyst Eng. 2020 Jul;43(7):1153-1169. doi: 10.1007/s00449-020-02311-x. Epub 2020 Feb 24.

Abstract

This study aimed to enhance the crystallizability of bio-based succinic acid for its efficient recovery while maintaining the end product at the highest purity. Immobilization of Actinobacillus succinogenes was initially evaluated based on three different carriers: volcanic glass, clay pebbles, and silica particles. The adsorption capacity of metabolites with a low concentration (10 g/L) and a high concentration (40 g/L) was investigated. It was demonstrated that clay pebbles adsorbed the least succinic acid (< 11 mg/g clay pebbles). The repeated batch-fermentation trials with immobilized cells highlighted that succinic acid with an average concentration of up to 36.3 g/L with a metabolite-production ratio of 3:1 (succinic acid to by-products) could be attained within 130 h. Subsequently, the purification of succinic acid through crystallization was assessed in terms of pH, temperature, crystallization time, initial succinic acid concentration and multiple recrystallization processes. Increasing the crystallization time from 6 h to 9 h afforded an improvement of 17% in the recovery of succinic acid crystals. Moreover, a fourfold concentration coefficient of the broth yielded the highest purity percentage (99.9%). The crystallization in three consecutive stages at 9 h (with a fourfold concentration coefficient) successfully improved the total recovery percentage of succinic acid from 55.0 to 84.8%.

摘要

本研究旨在提高生物基琥珀酸的结晶能力,以便在保持最终产品最高纯度的同时有效回收琥珀酸。首先评估了三种不同载体(火山玻璃、陶粒和硅胶颗粒)对发酵液中琥珀酸的吸附能力。研究了低浓度(10 g/L)和高浓度(40 g/L)下琥珀酸代谢产物的吸附能力。结果表明,陶粒对琥珀酸的吸附能力最低(<11 mg/g 陶粒)。采用固定化细胞进行重复分批发酵实验,结果表明,在 130 h 内可达到平均浓度高达 36.3 g/L,琥珀酸与副产物的产率比为 3:1。随后,从 pH 值、温度、结晶时间、初始琥珀酸浓度和多次重结晶过程等方面评估了琥珀酸通过结晶进行纯化的效果。将结晶时间从 6 h 延长至 9 h,可使琥珀酸晶体的回收率提高 17%。此外,将发酵液浓缩 4 倍可得到最高纯度(99.9%)的琥珀酸。在 9 h 内分三个阶段进行结晶(浓缩 4 倍)可将琥珀酸的总回收率从 55.0%提高到 84.8%。

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