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钠离子激活磷酸果糖激酶,导致以氢氧化钠作为中和剂时,菊糖芽孢乳杆菌产生的D-乳酸增加。

Sodium ions activated phosphofructokinase leading to enhanced D-lactic acid production by Sporolactobacillus inulinus using sodium hydroxide as a neutralizing agent.

作者信息

Zheng Lu, Liu Mingqing, Sun Jiaduo, Wu Bin, He Bingfang

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, Jiangsu, 211816, China.

State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, Jiangsu, 210008, China.

出版信息

Appl Microbiol Biotechnol. 2017 May;101(9):3677-3687. doi: 10.1007/s00253-017-8120-0. Epub 2017 Feb 11.

Abstract

Sporolactobacillus inulinus is a superior D-lactic acid-producing bacterium and proposed species for industrial production. The major pathway for D-lactic acid biosynthesis, glycolysis, is mainly regulated via the two irreversible steps catalyzed by the allosteric enzymes, phosphofructokinase (PFK) and pyruvate kinase. The activity level of PFK was significantly consistent with the cell growth and D-lactic acid production, indicating its vital role in control and regulation of glycolysis. In this study, the ATP-dependent PFK from S. inulinus was expressed in Escherichia coli and purified to homogeneity. The PFK was allosterically activated by both GDP and ADP and inhibited by phosphoenolpyruvate; the addition of activators could partly relieve the inhibition by phosphoenolpyruvate. Furthermore, monovalent cations could enhance the activity, and Na was the most efficient one. Considering this kind activation, NaOH was investigated as the neutralizer instead of the traditional neutralizer CaCO. In the early growth stage, the significant accelerated glucose consumption was achieved in the NaOH case probably for the enhanced activity of Na-activated PFK. Using NaOH as the neutralizer at pH 6.5, the fermentation time was greatly shortened about 22 h; simultaneously, the glucose consumption rate and the D-lactic acid productivity were increased by 34 and 17%, respectively. This probably contributed to the increased pH and Na-promoted activity of PFK. Thus, fermentations by S. inulinus using the NaOH neutralizer provide a green and highly efficient D-lactic acid production with easy subsequent purification.

摘要

菊糖芽孢乳杆菌是一种优良的D-乳酸生产菌,也是工业生产中拟用的菌种。D-乳酸生物合成的主要途径即糖酵解,主要通过变构酶磷酸果糖激酶(PFK)和丙酮酸激酶催化的两个不可逆步骤进行调控。PFK的活性水平与细胞生长及D-乳酸产量显著相关,表明其在糖酵解的控制和调节中起着至关重要的作用。在本研究中,菊糖芽孢乳杆菌的ATP依赖性PFK在大肠杆菌中表达并纯化至均一。该PFK受到GDP和ADP的变构激活,并受到磷酸烯醇丙酮酸的抑制;添加激活剂可部分缓解磷酸烯醇丙酮酸的抑制作用。此外,单价阳离子可增强其活性,其中Na+最为有效。基于这种激活作用,研究了用NaOH替代传统中和剂CaCO₃。在生长早期,使用NaOH时葡萄糖消耗显著加速,这可能是由于Na+激活的PFK活性增强。在pH 6.5条件下使用NaOH作为中和剂,发酵时间大幅缩短约22小时;同时,葡萄糖消耗速率和D-乳酸生产率分别提高了34%和17%。这可能归因于pH值的升高以及Na+对PFK活性的促进作用。因此,菊糖芽孢乳杆菌使用NaOH中和剂进行发酵可实现绿色高效的D-乳酸生产,且后续纯化简便。

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