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原生微藻中碳酸酐酶活性在 CO2 捕集中的应用证据。

An Evidence of Carbonic Anhydrase Activity in Native Microalgae for CO Capture Application.

机构信息

School of Life Sciences, B.S. Abdur Rahman Crescent Institute of Science and Technology, Chennai, 600048, India.

Crescent Global Outreach Mission (CGOM), B.S. Abdur Rahman Crescent Institute of Science and Technology, Chennai, 600048, India.

出版信息

Appl Biochem Biotechnol. 2024 Oct;196(10):7064-7073. doi: 10.1007/s12010-024-04908-4. Epub 2024 Mar 13.

Abstract

A promising alternative for effective carbon capture has been found in microalgae because of their high photosynthetic capacity and quick growth. The carbon concentration mechanism of many microalgae is heavily reliant on the enzyme carbonic anhydrase (CA), which catalyze the production of bicarbonate from carbon dioxide. In this study, microalgal samples were collected, characterized, and cultured under controlled conditions for their optimal growth of cultures I-IX. The CA activity was investigated using a standard method; the Wilbur-Anderson assay was used to calculate CA activity in microalgal cultures. The comparative study was then used to measure the activity rate of the collected microalgae. Among the tested, culture I, VI, and IX showed a high enzyme activity rate of 4.15, 4.0, and 4.2 µg·mL, respectively. To determine the rate of carbon dioxide hydration, the method involved tracking the pH change in a reaction mixture. In addition, genetic analysis facilitates the identification of key genes involved in CA activity and other metabolic processes, which enhance the knowledge of microalgal physiology, and enables genetic engineering efforts in the future studies. Overall, this investigation emphasizes the significance of studying unknown microalgal culture and their potential CA activity for industrial and bio-energy applications.

摘要

由于具有高光合能力和快速生长的特点,微藻已成为一种很有前途的有效碳捕获替代方法。许多微藻的碳浓缩机制严重依赖于碳酸酐酶 (CA) 这种酶,它可以催化二氧化碳生成碳酸氢盐。在这项研究中,收集了微藻样本,在受控条件下对其进行了特征描述和培养,以获得最佳的培养物 I-IX 生长。使用标准方法研究 CA 活性;使用 Wilbur-Anderson 测定法测定微藻培养物中的 CA 活性。然后使用比较研究来测量收集到的微藻的活性率。在测试的微藻中,培养物 I、VI 和 IX 的酶活性率分别为 4.15、4.0 和 4.2µg·mL。为了确定二氧化碳水合的速率,该方法涉及跟踪反应混合物中 pH 值的变化。此外,遗传分析有助于确定参与 CA 活性和其他代谢过程的关键基因,这增强了对微藻生理学的了解,并为未来的研究提供了遗传工程方面的支持。总的来说,这项研究强调了研究未知微藻培养物及其潜在 CA 活性在工业和生物能源应用中的重要性。

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