Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme

The haloarchaeon Halorubrum lacusprofundi is among the few polyextremophilic organisms capable of surviving in one of the most extreme aquatic environments on Earth, the Deep Lake of Antarctica (−18 °C to +11.5 °C and 21–28%, w/v salt content). Hence, H. lacusprofundi has been proposed as a model fo...

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Published in:Microorganisms
Main Authors: Ram Karan, Sam Mathew, Reyhan Muhammad, Didier B. Bautista, Malvina Vogler, Jorg Eppinger, Romina Oliva, Luigi Cavallo, Stefan T. Arold, Magnus Rueping
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2020
Subjects:
Online Access:https://doi.org/10.3390/microorganisms8101594
https://doaj.org/article/3905025b238f47f185f87cf559905683
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spelling ftdoajarticles:oai:doaj.org/article:3905025b238f47f185f87cf559905683 2023-05-15T14:04:00+02:00 Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme Ram Karan Sam Mathew Reyhan Muhammad Didier B. Bautista Malvina Vogler Jorg Eppinger Romina Oliva Luigi Cavallo Stefan T. Arold Magnus Rueping 2020-10-01T00:00:00Z https://doi.org/10.3390/microorganisms8101594 https://doaj.org/article/3905025b238f47f185f87cf559905683 EN eng MDPI AG https://www.mdpi.com/2076-2607/8/10/1594 https://doaj.org/toc/2076-2607 doi:10.3390/microorganisms8101594 2076-2607 https://doaj.org/article/3905025b238f47f185f87cf559905683 Microorganisms, Vol 8, Iss 1594, p 1594 (2020) extremophiles halophiles psychrophiles polyextremophiles extremozymes X-ray crystallography Biology (General) QH301-705.5 article 2020 ftdoajarticles https://doi.org/10.3390/microorganisms8101594 2022-12-31T16:32:49Z The haloarchaeon Halorubrum lacusprofundi is among the few polyextremophilic organisms capable of surviving in one of the most extreme aquatic environments on Earth, the Deep Lake of Antarctica (−18 °C to +11.5 °C and 21–28%, w/v salt content). Hence, H. lacusprofundi has been proposed as a model for biotechnology and astrobiology to investigate potential life beyond Earth. To understand the mechanisms that allow proteins to adapt to both salinity and cold, we structurally (including X-ray crystallography and molecular dynamics simulations) and functionally characterized the β-galactosidase from H. lacusprofundi (hla_bga). Recombinant hla_bga (produced in Haloferax volcanii ) revealed exceptional stability, tolerating up to 4 M NaCl and up to 20% (v/v) of organic solvents. Despite being cold-adapted, hla_bga was also stable up to 60 °C. Structural analysis showed that hla_bga combined increased surface acidity (associated with halophily) with increased structural flexibility, fine-tuned on a residue level, for sustaining activity at low temperatures. The resulting blend enhanced structural flexibility at low temperatures but also limited protein movements at higher temperatures relative to mesophilic homologs. Collectively, these observations help in understanding the molecular basis of a dual psychrophilic and halophilic adaptation and suggest that such enzymes may be intrinsically stable and functional over an exceptionally large temperature range. Article in Journal/Newspaper Antarc* Antarctica Directory of Open Access Journals: DOAJ Articles Microorganisms 8 10 1594
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic extremophiles
halophiles
psychrophiles
polyextremophiles
extremozymes
X-ray crystallography
Biology (General)
QH301-705.5
spellingShingle extremophiles
halophiles
psychrophiles
polyextremophiles
extremozymes
X-ray crystallography
Biology (General)
QH301-705.5
Ram Karan
Sam Mathew
Reyhan Muhammad
Didier B. Bautista
Malvina Vogler
Jorg Eppinger
Romina Oliva
Luigi Cavallo
Stefan T. Arold
Magnus Rueping
Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme
topic_facet extremophiles
halophiles
psychrophiles
polyextremophiles
extremozymes
X-ray crystallography
Biology (General)
QH301-705.5
description The haloarchaeon Halorubrum lacusprofundi is among the few polyextremophilic organisms capable of surviving in one of the most extreme aquatic environments on Earth, the Deep Lake of Antarctica (−18 °C to +11.5 °C and 21–28%, w/v salt content). Hence, H. lacusprofundi has been proposed as a model for biotechnology and astrobiology to investigate potential life beyond Earth. To understand the mechanisms that allow proteins to adapt to both salinity and cold, we structurally (including X-ray crystallography and molecular dynamics simulations) and functionally characterized the β-galactosidase from H. lacusprofundi (hla_bga). Recombinant hla_bga (produced in Haloferax volcanii ) revealed exceptional stability, tolerating up to 4 M NaCl and up to 20% (v/v) of organic solvents. Despite being cold-adapted, hla_bga was also stable up to 60 °C. Structural analysis showed that hla_bga combined increased surface acidity (associated with halophily) with increased structural flexibility, fine-tuned on a residue level, for sustaining activity at low temperatures. The resulting blend enhanced structural flexibility at low temperatures but also limited protein movements at higher temperatures relative to mesophilic homologs. Collectively, these observations help in understanding the molecular basis of a dual psychrophilic and halophilic adaptation and suggest that such enzymes may be intrinsically stable and functional over an exceptionally large temperature range.
format Article in Journal/Newspaper
author Ram Karan
Sam Mathew
Reyhan Muhammad
Didier B. Bautista
Malvina Vogler
Jorg Eppinger
Romina Oliva
Luigi Cavallo
Stefan T. Arold
Magnus Rueping
author_facet Ram Karan
Sam Mathew
Reyhan Muhammad
Didier B. Bautista
Malvina Vogler
Jorg Eppinger
Romina Oliva
Luigi Cavallo
Stefan T. Arold
Magnus Rueping
author_sort Ram Karan
title Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme
title_short Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme
title_full Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme
title_fullStr Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme
title_full_unstemmed Understanding High-Salt and Cold Adaptation of a Polyextremophilic Enzyme
title_sort understanding high-salt and cold adaptation of a polyextremophilic enzyme
publisher MDPI AG
publishDate 2020
url https://doi.org/10.3390/microorganisms8101594
https://doaj.org/article/3905025b238f47f185f87cf559905683
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Microorganisms, Vol 8, Iss 1594, p 1594 (2020)
op_relation https://www.mdpi.com/2076-2607/8/10/1594
https://doaj.org/toc/2076-2607
doi:10.3390/microorganisms8101594
2076-2607
https://doaj.org/article/3905025b238f47f185f87cf559905683
op_doi https://doi.org/10.3390/microorganisms8101594
container_title Microorganisms
container_volume 8
container_issue 10
container_start_page 1594
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