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...
Published in: | Microorganisms |
---|---|
Main Authors: | , , , , , , , , , |
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 |
id |
ftdoajarticles:oai:doaj.org/article:3905025b238f47f185f87cf559905683 |
---|---|
record_format |
openpolar |
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 |
_version_ |
1766274938007715840 |