Abstract

During industrial yeast production, cells are often subjected to deleterious hydric variations during dehydration, which reduces their viability and cellular activity. This study is focused on the yeast Lachancea thermotolerans, particularly sensitive to dehydration. The aim was to understand the modifications of single-cells biophysical profiles during different dehydration conditions. Infrared spectra of individual cells were acquired before and after dehydration kinetics using synchrotron radiation-based Fourier-transform infrared (S-FTIR) microspectroscopy. The cells were previously stained with fluorescent probes in order to measure only viable and active cells prior to dehydration. In parallel, cell viability was determined using flow cytometry under identical conditions. The S-FTIR analysis indicated that cells with the lowest viability showed signs of membrane rigidification and modifications in the amide I (α-helix and β-sheet) and amide II, which are indicators of secondary protein structure conformation and degradation or disorder. Shift of symmetric C–H stretching vibration of the CH2 group upon a higher wavenumber correlated with better cell viability, suggesting a role of plasma membrane fluidity. This was the first time that the biophysical responses of L. thermotolerans single-cells to dehydration were explored with S-FTIR. These findings are important for clarifying the mechanisms of microbial resistance to stress in order to improve the viability of sensitive yeasts during dehydration.

Highlights

  • Dehydration processes are a crucial part of yeast industrial usage

  • It was previously shown that S. cerevisiae yeast cells grown in nutrientrich media were more resistant to dehydration performed in a fluidized bed (Câmara, 2018) or L. thermotolerans cells under controlled air humidity (Câmara et al, 2018, 2019b) both in a dehydration temperature dependent manner

  • Increasing contact time of the cells with the drying air increases the yeast oxidative stress, which partially explains the reduced cell viability in the control samples (71%) (Câmara et al, 2019b). It was shown with different wine yeast S. cerevisiae strains that a dehydration cycle of h at 30◦C and 8% relative humidity (RH) caused from to 65% of cell death according to the strain (Gamero-Sandemetrio et al, 2014)

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Summary

Introduction

Dehydration processes are a crucial part of yeast industrial usage. These processes involve different steps that may interfere with the yeasts’ cellular activity. Removal of water by dry-air and elevated temperatures generate modifications in the water potential of the medium and in the cells themselves, leading to a decrease in their volume and an increase of their contact surface with air (Beker and Rapoport, 1987; Gervais and Beney, 2001; Lemetais et al, 2012; Rapoport et al, 2016). All these modifications can induce the accumulation of reactive oxygen species (ROS), oxidative stress and cause the cells death (Eleutherio et al, 2018)

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