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利用工程化 评价从红海藻类水解物中生产 2,3-丁二醇

Evaluation of 2,3-Butanediol Production from Red Seaweed Hydrolysates Using Engineered .

机构信息

Department of Food Science and Biotechnology, College of Engineering, Global K-Food Research Center, Hankyong National University, Anseong 17579, Republic of Korea.

Department of Agricultural Biotechnology and Center for Food and Bioconvergence, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2020 Dec 28;30(12):1912-1918. doi: 10.4014/jmb.2007.07037.

DOI:10.4014/jmb.2007.07037
PMID:32958731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9728296/
Abstract

Hyper-thermal (HT) acid hydrolysis of red seaweed was performed using 12% (w/v) slurry and an acid mix concentration of 180 mM at 150°C for 10 min. Enzymatic saccharification when using a combination of Celluclast 1.5 L and CTec2 at a dose of 16 U/ml led to the production of 12.0 g/l of reducing sugar with an efficiency of enzymatic saccharification of 13.2%. After the enzymatic saccharification, 2,3-butanediol (2,3-BD) fermentation was carried out using an engineered strain. The use of HT acid-hydrolyzed medium with 1.9 g/l of 5-hydroxymethylfurfural showed a reduction in the lag time from 48 to 24 h. The 2,3-BD concentration and yield coefficient at 72 h were 14.8 g/l and 0.30, respectively. Therefore, HT acid hydrolysis and the use of the engineered strain can enhance the overall 2,3-BD yields from seaweed.

摘要

采用 12%(w/v)的料浆和 180mM 的酸混合浓度,在 150°C 下对红海藻类进行超热(HT)酸水解 10 分钟。使用纤维素酶 1.5 L 和 CTec2 的组合,剂量为 16U/ml,进行酶解,可产生 12.0g/L 的还原糖,酶解效率为 13.2%。酶解后,采用工程化菌株进行 2,3-丁二醇(2,3-BD)发酵。使用 HT 酸水解培养基,其中含有 1.9g/L 的 5-羟甲基糠醛,可将迟滞时间从 48 小时缩短至 24 小时。72 小时时,2,3-BD 的浓度和产率系数分别为 14.8g/L 和 0.30。因此,HT 酸水解和工程化菌株的使用可以提高海藻中 2,3-BD 的总产率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/e9a61df765a8/JMB-30-12-1912-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/697dea0009a4/JMB-30-12-1912-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/32e136246ac9/JMB-30-12-1912-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/14dbfb30895a/JMB-30-12-1912-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/e9a61df765a8/JMB-30-12-1912-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/697dea0009a4/JMB-30-12-1912-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/32e136246ac9/JMB-30-12-1912-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/14dbfb30895a/JMB-30-12-1912-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d31/9728296/e9a61df765a8/JMB-30-12-1912-f4.jpg

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