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Adaptation of Folding and Function of a Nuclease from the Cold Deep Sea
Article de revue scientifique   Avec comité de lecture

Adaptation of Folding and Function of a Nuclease from the Cold Deep Sea

Tejaswi Koduru, Philippe Barthe, Noam Hantman, Karine De Guillen, Scott A. McCallum, Joel E. Morgan, Estella F. Yee, Pierce Leonardi, Jack Foland, Christian Roumestand, …
Journal of molecular biology, Vol.438(4), p.169602
15/02/2026
PMID: 41443464

Résumé

activity biophysical characterization folding piezophile psychrophile
[Display omitted] •Cnase sequence was found in an organism isolate at 2500 m depth and 2 °C.•Cnase is a bonafide, albeit slow exonuclease, despite being highly negatively charged.•Cnase largely conserves the structure of the mesophilic homolog Snase.•Cnase also conserves the folding mechanism of Snase, despite their differences in sequence. The majority of the Earth’s microbial biomass is found in high pressure environments, raising the question of how protein sequences adapt to such environments. Pressure adaptation is more complex, and less well-understood, than adaptation to extreme temperatures since in high pressure environments, these two thermodynamic parameters are often coupled, as in the cold deep-sea or at hydrothermal vents. To begin to address this question, we investigated the functional and folding properties of an exonuclease, Cnase, from the first Gram positive piezophile to be sequenced, Carnobacterium sp. AT7, isolated at 2500 m depth and at ∼2 °C in the Aleutian trench in the North Pacific. We find that Cnase is a bonafide exonuclease, despite its high negative charge. We also find that Cnase largely conserves the structure and folding mechanism of its mesophilic and well-studied homolog, staphylococcal nuclease, Snase, despite significant differences in their sequences.

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