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Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK
Caseinolytic proteins (Clp), which are present in both prokaryotes and eukaryotes, play a major role in cell protein quality control and survival of bacteria in harsh environmental conditions. Recently, a member of this protein family, ClpK was identified in a pathogenic strain of Klebsiella pneumon...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746953/ https://www.ncbi.nlm.nih.gov/pubmed/35011428 http://dx.doi.org/10.3390/molecules27010200 |
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author | Motiwala, Tehrim Akumadu, Blessing Oluebube Zuma, Sbahle Mfeka, Mbalenhle Sizamile Chen, Wanping Achilonu, Ikechukwu Syed, Khajamohiddin Khoza, Thandeka |
author_facet | Motiwala, Tehrim Akumadu, Blessing Oluebube Zuma, Sbahle Mfeka, Mbalenhle Sizamile Chen, Wanping Achilonu, Ikechukwu Syed, Khajamohiddin Khoza, Thandeka |
author_sort | Motiwala, Tehrim |
collection | PubMed |
description | Caseinolytic proteins (Clp), which are present in both prokaryotes and eukaryotes, play a major role in cell protein quality control and survival of bacteria in harsh environmental conditions. Recently, a member of this protein family, ClpK was identified in a pathogenic strain of Klebsiella pneumoniae which was responsible for nosocomial infections. ClpK is linked to the thermal stress survival of this pathogen. The genome wide analysis of Clp proteins in Klebsiella spp. indicates that ClpK is present in only 34% of the investigated strains. This suggests that the uptake of the clpk gene is selective and may only be taken up by a pathogen that needs to survive harsh environmental conditions. In silico analyses and molecular dynamic simulations show that ClpK is mainly α-helical and is highly dynamic. ClpK was successfully expressed and purified to homogeneity using affinity and anion exchange chromatography. Biophysical characterization of ClpK showed that it is predominantly alpha-helical, and this is in agreement with in silico analysis of the protein structure. Furthermore, the purified protein is biologically active and hydrolyses ATP in a concentration- dependent manner. |
format | Online Article Text |
id | pubmed-8746953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87469532022-01-11 Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK Motiwala, Tehrim Akumadu, Blessing Oluebube Zuma, Sbahle Mfeka, Mbalenhle Sizamile Chen, Wanping Achilonu, Ikechukwu Syed, Khajamohiddin Khoza, Thandeka Molecules Article Caseinolytic proteins (Clp), which are present in both prokaryotes and eukaryotes, play a major role in cell protein quality control and survival of bacteria in harsh environmental conditions. Recently, a member of this protein family, ClpK was identified in a pathogenic strain of Klebsiella pneumoniae which was responsible for nosocomial infections. ClpK is linked to the thermal stress survival of this pathogen. The genome wide analysis of Clp proteins in Klebsiella spp. indicates that ClpK is present in only 34% of the investigated strains. This suggests that the uptake of the clpk gene is selective and may only be taken up by a pathogen that needs to survive harsh environmental conditions. In silico analyses and molecular dynamic simulations show that ClpK is mainly α-helical and is highly dynamic. ClpK was successfully expressed and purified to homogeneity using affinity and anion exchange chromatography. Biophysical characterization of ClpK showed that it is predominantly alpha-helical, and this is in agreement with in silico analysis of the protein structure. Furthermore, the purified protein is biologically active and hydrolyses ATP in a concentration- dependent manner. MDPI 2021-12-29 /pmc/articles/PMC8746953/ /pubmed/35011428 http://dx.doi.org/10.3390/molecules27010200 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Motiwala, Tehrim Akumadu, Blessing Oluebube Zuma, Sbahle Mfeka, Mbalenhle Sizamile Chen, Wanping Achilonu, Ikechukwu Syed, Khajamohiddin Khoza, Thandeka Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK |
title | Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK |
title_full | Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK |
title_fullStr | Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK |
title_full_unstemmed | Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK |
title_short | Caseinolytic Proteins (Clp) in the Genus Klebsiella: Special Focus on ClpK |
title_sort | caseinolytic proteins (clp) in the genus klebsiella: special focus on clpk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746953/ https://www.ncbi.nlm.nih.gov/pubmed/35011428 http://dx.doi.org/10.3390/molecules27010200 |
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