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Biology subjects

Gault, S.

Publications and source records attributed to Gault, S..

2 recordsLinked to original sources

Large datasets and machine learning models fail to capture extremophile enzyme melting and optimum temperatures

Organisms and their enzymes adapt to environmental temperatures, such that thermophilic enzymes exhibit high melting and optimum temperatures while psychrophilic enzymes exhibit low values for both. It has been proposed that the gap between an enzymes optimum temperature and its melting temperature, the temperature gap, is characteristically large in psychrophiles, implying that the loss of activity above the optimum is decoupled from global protein stability. The evidence for this relies on a small number of characterised enzymes, leaving the prevalence of large temperature gaps amongst psychrophiles unknown. We asked whether the machine-learning predictors and large datasets now available could test this at scale. We find that they cannot: predictors of melting and optimum temperature fail systematically at the thermal extremes, assigning the majority of thermophilic enzymes with optimum temperatures that exceed their melting temperatures, which is biophysically implausible, and consistently underpredict the stability of (hyper)thermophiles. This stems from training data that is both error-laden, as we demonstrate for widely used optimum-temperature records, and overwhelmingly biased toward mesophiles, which regresses predictions for cold and heat adapted enzymes toward mesophilic values. Consequently, current computational tools cannot establish how prevalent the psychrophilic temperature gap is. We argue that proteome-scale measurement of extremophile enzyme thermal behaviour, integrated as curated training data, is required to determine whether trends from small studies extend across the diversity of life.

biochemistry↗

High pressures depress the onset of intracellular vitrification

The low temperature limit for life remains elusive and poorly understood. This ignorance is further compounded when applied to life in multi-extreme environments where low temperatures combine with factors such as high salt concentrations, or high environmental pressures. It has been proposed that the onset of intracellular vitrification enforces a biophysical low temperature limit for unicellular life at [~] -23 {degrees}C. However, it has not been demonstrated how high-pressures affect intracellular vitrification, which is vital for understanding the habitability of low temperature, subsurface environments, both on Earth and on other planetary bodies. Here, we used high-pressure differential scanning calorimetry to measure the intracellular vitrification of Bacillus subtilis across pressures ranging from 1 to 1000 bar. We find that high pressures depress the onset of intracellular vitrification in a pressure dependent manner, which is tightly correlated with the ability of pressure to depress the freezing point of water. Additionally, we show that sub-molar concentrations of NaCl can act in combination with high pressures to further depress intracellular vitrification, highlighting the interplay between temperature, pressure, and ions in influencing the physical state of cells in natural environments. These results show that cells in subzero high-pressure environments would be liquidous, and potentially metabolically active, and not merely vitrified and preserved. Additionally, our results provide considerations in the preparation of biological samples through high-pressure freezing for electron microscopy, particularly those associated with high concentrations of cryoprotectants.

microbiology↗