Inactivation and structural alteration of α-amylase by low-pressure carbon dioxide microbubbles. (January 2020)

• Record Type: Journal Article
• Authors: Kobayashi, Fumiyuki; Nakajima, Risa; Narai-Kanayama, Asako; Odake, Sachiko
• Is Part Of: Process biochemistry. Volume 88(2020)
• Page Start: 60
• Page End: 66
• Publication Date: 2020-01
• Subjects: α-Amylase -- Fluorescence analysis -- Inactivation -- Low-pressure carbon dioxide microbubbles -- Polyacrylamide gel electrophoresis; Biochemical engineering -- Periodicals; Biotechnology -- Periodicals; Biochemistry -- periodicals; Biotechnology -- periodicals; Chemical Engineering -- periodicals; Génie biochimique -- Périodiques; Biotechnologie -- Périodiques; Biochemical engineering; Biotechnology; Periodicals; 660.63
• DOI: 10.1016/j.procbio.2019.10.017
• Languages: English
• ISSNs: 1359-5113

Abstract

Graphical abstract: Highlights: Low-pressure carbon dioxide microbubbles (CO2 MB) was able to inactivate α-amylase. Inactivation of α-amylase by CO2 MB was more effective than thermal treatment. The CO2 MB induced the structural alteration of α-amylase. The inactivation by CO2 MB was related to the alteration of the tertiary structure. Abstract: The efficiency of low-pressure carbon dioxide microbubbles (CO2 MB) to inactivate α-amylase was analysed kinetically, and structural alteration of α-amylase by CO2 MB was investigated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and fluorescence analysis of tryptophan (Trp) residues. Activity and Trp fluorescence intensity of α-amylase treated by CO2 MB decreased with increasing temperature, pressure and exposure time, and lowering the initial buffer pH, respectively. In the kinetic analysis, it was confirmed that the decreased temperature-dependency and increased activation energy associated with the inactivation of α-amylase by CO2 MB were induced by pressurizing the mixing vessel and that the decreased pressure-dependency and increased activation volume concomitant to the inactivation of α-amylase by CO2 MB was induced by increasing the temperature in the heating coil. In SDS-PAGE, CO2 MB was suggested to induce the structural alteration of α-amylase because the band density decreased after CO2 MB treatment, although this phenomenon was not related to the inactivation efficiency. However, Trp fluorescence analysis showed that the alteration of the tertiary structure of α-amylase by CO2 MB was related to the inactivation efficiency. Therefore, CO2 MB was more effective than thermal treatment in inactivating α-amylase, and the inactivation efficiency was suggested to be related to the alteration of the enzyme's tertiary structure.