4.7 Article

Lipase-Ca2+ hybrid nanobiocatalysts through interfacial protein-inorganic self-assembly in deep-eutectic solvents (DES)/water two-phase system for biodiesel production

Journal

RENEWABLE ENERGY
Volume 197, Issue -, Pages 110-124

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2022.07.092

Keywords

Lipase immobilization; Biodiesel production; Deep -eutectic solvents; Interfacial effect; Two-phase system

Funding

  1. Science and Technology Program of Tianjin, China [2020YJSB122]
  2. Key Pro- jects of Tianjin Natural Science Foundation, China [19JCZDJC38100]
  3. National Natural Science Foundation of China [2020YJSB122]
  4. Key Projects of Tianjin Natural Science Foundation, China [20ZYJDJC00080]
  5. National Natural Science Foundation of China [19JCZDJC38100]
  6. Open Funding Project of the State Key Laboratory of Biocatalysis and Enzyme Engineering, China [22108206]
  7. Innovation Project of Excellent Doctoral Dissertation of Tianjin University of Science and Technology [SKLBEE2021002, 2020009]
  8. Postgraduate Research Innovation project of Tianjin [2019010]

Ask authors/readers for more resources

A novel lipase hybrid biocatalyst with superior catalytic activity and stability was developed through dual activation of calcium ions and deep-eutectic solvents. Compared to free lipase, this catalyst exhibited improved substrate selectivity, tolerance to chemical denaturants, and reusability.
The production of biodiesel catalyzed by lipase has the advantages of simple process, low energy consumption, and low wastewater treatment requirements. However, low activity, poor stability, and difficulty in recycling still limit the application of lipase in production of biodiesel. Herein, a novel lipase hybrid biocatalyst with superior catalytic activity and stability (lipase from Aspergillus oryzae CJLU-3, AOCL@CaP in DES) was developed by dual activation of Ca2+ and interfacial effect of deep-eutectic solvents (DES)/water two-phase system. AOCL@CaP in DES exhibited significantly enhanced enzymatic activity with a Kcat/Km value of 692 s-1 mM(-1) and excellent thermostability, tolerance to chemical denaturants, substrate selectivity, and reusability compared with free lipase. Recovery activity of the prepared hybrid biocatalyst in pure water system (AOCL@CaP) and AOCL@CaP in DES was 195% and 250% using p-NPL as substrate, respectively. AOCL@CaP in DES exhibited about 253% of the original activity after 100 days of storage, while free AOCL, AOCL@CaP almost completely lost activity. The FAME content in product biodiesel catalyzed from soybean oil by AOCL@CaP was only 60%, However, the FAME content catalyzed by AOCL@CaP in DES reached 87%, and could be maintained at 50% even after 10 cycles.

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