Enhancement of antroquinonol production during batch fermentation using pH control coupled with an oxygen vector

J Sci Food Agric. 2019 Jan 15;99(1):449-456. doi: 10.1002/jsfa.9206. Epub 2018 Sep 13.

Abstract

Background: Antroquinonol, a ubiquinone derivative that shows anticancer and anti-inflammatory activities, is produced during solid-state fermentation of Antrodia camphorata; however, it cannot be biosynthesized via conventional submerged fermentation.

Results: A method for enhancing the biosynthesis of antroquinonol by controlling pH and adding an oxygen vector in a 7 L bioreactor was studied. In shake-flask experiments, a maximum antroquinonol production of 31.39 ± 0.78 mg L-1 was obtained by fermentation with adding 0.2 g L-1 coenzyme Q0 (CoQ0 ), at the 96th hour. Following kinetic analysis of the fermentation process, pH control strategies were investigated. A maximum antroquinonol production of 86.47 ± 3.65 mg L-1 was achieved when the pH was maintained at 5.0, which exhibited an increase of 348.03% higher than the batch without pH regulation (19.30 ± 0.88 mg L-1 ). The conversion rate of CoQ0 improved from 1.51% to 20.20%. Further research revealed that the addition of n-tetradecane could increase the production of antroquinonol to 115.62 ± 4.87 mg L-1 by increasing the dissolved oxygen in the fermentation broth.

Conclusion: The results demonstrated that pH played an important role in antroquinonol synthesis in the presence of the effective precursor CoQ0 . It was a very effective strategy to increase the yield of antroquinonol by controlling pH and adding oxygen vector. © 2018 Society of Chemical Industry.

Keywords: Antrodia camphorata; antroquinonol; n-tetradecane; oxygen vector; pH control.

Publication types

  • Evaluation Study

MeSH terms

  • Antrodia / metabolism*
  • Batch Cell Culture Techniques / instrumentation
  • Batch Cell Culture Techniques / methods*
  • Bioreactors / microbiology
  • Culture Media / chemistry*
  • Culture Media / metabolism
  • Fermentation
  • Hydrogen-Ion Concentration
  • Oxygen / analysis
  • Oxygen / metabolism*
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / biosynthesis
  • Ubiquinone / metabolism

Substances

  • Culture Media
  • Ubiquinone
  • antroquinonol
  • Ubiquinone Q1
  • Oxygen