Non-invasive monitoring of microbial triterpenoid production using nonlinear microscopy techniques

Front Bioeng Biotechnol. 2023 Feb 28:11:1106566. doi: 10.3389/fbioe.2023.1106566. eCollection 2023.

Abstract

Introduction: Bioproduction of plant-derived triterpenoids in recombinant microbes is receiving great attention to make these biologically active compounds industrially accessible as nutraceuticals, pharmaceutics, and cosmetic ingredients. So far, there is no direct method for detecting triterpenoids under physiological conditions on a cellular level, information yet highly relevant to rationalizing microbial engineering. Methods: Here, we show in a proof-of-concept study, that triterpenoids can be detected and monitored in living yeast cells by combining coherent anti-Stokes Raman scattering (CARS) and second-harmonic-generation (SHG) microscopy techniques. We applied CARS and SHG microscopy measurements, and for comparison classical Nile Red staining, on immobilized and growing triterpenoid-producing, and non-producing reference Saccharomyces cerevisiae strains. Results and Discussion: We found that the SHG signal in triterpenoid-producing strains is significantly higher than in a non-producing reference strain, correlating with lipophile content as determined by Nile red staining. In growing cultures, both CARS and SHG signals showed changes over time, enabling new insights into the dynamics of triterpenoid production and storage inside cells.

Keywords: CARS microscopy; baker’s yeast; lipids; metabolic engineering; natural compounds; second harmonic generation.

Grants and funding

This research was performed within the project PRODIGY (process-directed drug generation in yeast) funded by the German Federal Ministry of Education and Research BMBF (grant No. 031B0356B). We would like to share our gratitude to our project partners Prof. Dr. Markus Nett and Anna Tippelt (Department of Biochemical and Chemical Engineering, Laboratory of Technical Biology, TU Dortmund University) for their support and enabling us to perform our yeast cultivations in their laboratory.