Characterization of esterase activity from an Acetomicrobium hydrogeniformans enzyme with high structural stability in extreme conditions

• Published in: Extremophiles : life under extreme conditions Vol. 22; no. 5; pp. 781 - 793
• Main Authors: Kumagai, Patricia S., Gutierrez, Raissa F., Lopes, Jose L. S., Martins, Julia M., Jameson, David M., Castro, Aline M., Martins, Luiz F., DeMarco, Ricardo, Bossolan, Nelma R. S., Wallace, B. A., Araujo, Ana P. U.
• Format: Journal Article
• Language: English
• Published: Tokyo Springer Japan 01.09.2018; Springer Nature B.V
• Subjects: Biochemistry; Biomedical and Life Sciences; Biotechnology; Carbonates; Catalysis; Catalytic activity; Circular dichroism; Dichroism; E coli; Enhanced oil recovery; Enzymes; Esterase; Esterases; Fluorescence; High temperature; Industrial applications; Life Sciences; Microbial Ecology; Microbiology; Microbiota; Oil recovery; Oil reservoirs; Organic solvents; Original Paper; Recombinants; Solvents; Space life sciences; Stability; Structural stability; Substrates; Synchrotron radiation; Wettability; Fluorescence spectroscopy; Protein stability; Enhanced oil recovery (EOR); Esterase; Synchrotron radiation circular dichroism (SRCD) spectroscopy
• ISSN: 1431-0651; 1433-4909
• DOI: 10.1007/s00792-018-1038-3

The biotechnological and industrial uses of thermostable and organic solvent-tolerant enzymes are extensive and the investigation of such enzymes from microbiota present in oil reservoirs is a promising approach. Searching sequence databases for esterases from such microbiota, we have identified in silico a potentially secreted esterase from Acetomicrobium hydrogeniformans , named AhEst. The recombinant enzyme was produced in E. coli to be used in biochemical and biophysical characterization studies. AhEst presented hydrolytic activity on short-acyl-chain p -nitrophenyl ester substrates. AhEst activity was high and stable in temperatures up to 75 °C. Interestingly, high salt concentration induced a significant increase of catalytic activity. AhEst still retained ~ 50% of its activity in 30% concentration of several organic solvents. Synchrotron radiation circular dichroism and fluorescence spectroscopies confirmed that AhEst displays high structural stability in extreme conditions of temperature, salinity, and organic solvents. The enzyme is a good emulsifier agent and is able to partially reverse the wettability of an oil-wet carbonate substrate, making it of potential interest for use in enhanced oil recovery. All the traits observed in AhEst make it an interesting candidate for many industrial applications, such as those in which a significant hydrolytic activity at high temperatures is required.