Cargando…
Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool
The advent of metagenomics has greatly facilitated the discovery of enzymes with useful biochemical characteristics for industrial and biomedical applications, from environmental niches. In this study, we used sequence‐based metagenomics to identify two antibiotic resistance enzymes from the seclude...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270753/ https://www.ncbi.nlm.nih.gov/pubmed/28004885 http://dx.doi.org/10.1111/1751-7915.12468 |
_version_ | 1782501225894248448 |
---|---|
author | Elbehery, Ali H. A. Leak, David J. Siam, Rania |
author_facet | Elbehery, Ali H. A. Leak, David J. Siam, Rania |
author_sort | Elbehery, Ali H. A. |
collection | PubMed |
description | The advent of metagenomics has greatly facilitated the discovery of enzymes with useful biochemical characteristics for industrial and biomedical applications, from environmental niches. In this study, we used sequence‐based metagenomics to identify two antibiotic resistance enzymes from the secluded, lower convective layer of Atlantis II Deep Red Sea brine pool (68°C, ~2200 m depth and 250‰ salinity). We assembled > 4 000 000 metagenomic reads, producing 43 555 contigs. Open reading frames (ORFs) called from these contigs were aligned to polypeptides from the Comprehensive Antibiotic Resistance Database using BLASTX. Two ORFs were selected for further analysis. The ORFs putatively coded for 3′‐aminoglycoside phosphotransferase [APH(3′)] and a class A beta‐lactamase (ABL). Both genes were cloned, expressed and characterized for activity and thermal stability. Both enzymes were active in vitro, while only APH(3′) was active in vivo. Interestingly, APH(3′) proved to be thermostable (T (m) = 61.7°C and ~40% residual activity after 30 min of incubation at 65°C). On the other hand, ABL was not as thermostable, with a T (m) = 43.3°C. In conclusion, we have discovered two novel AR enzymes with potential application as thermophilic selection markers. |
format | Online Article Text |
id | pubmed-5270753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52707532017-02-01 Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool Elbehery, Ali H. A. Leak, David J. Siam, Rania Microb Biotechnol Research Articles The advent of metagenomics has greatly facilitated the discovery of enzymes with useful biochemical characteristics for industrial and biomedical applications, from environmental niches. In this study, we used sequence‐based metagenomics to identify two antibiotic resistance enzymes from the secluded, lower convective layer of Atlantis II Deep Red Sea brine pool (68°C, ~2200 m depth and 250‰ salinity). We assembled > 4 000 000 metagenomic reads, producing 43 555 contigs. Open reading frames (ORFs) called from these contigs were aligned to polypeptides from the Comprehensive Antibiotic Resistance Database using BLASTX. Two ORFs were selected for further analysis. The ORFs putatively coded for 3′‐aminoglycoside phosphotransferase [APH(3′)] and a class A beta‐lactamase (ABL). Both genes were cloned, expressed and characterized for activity and thermal stability. Both enzymes were active in vitro, while only APH(3′) was active in vivo. Interestingly, APH(3′) proved to be thermostable (T (m) = 61.7°C and ~40% residual activity after 30 min of incubation at 65°C). On the other hand, ABL was not as thermostable, with a T (m) = 43.3°C. In conclusion, we have discovered two novel AR enzymes with potential application as thermophilic selection markers. John Wiley and Sons Inc. 2016-12-22 /pmc/articles/PMC5270753/ /pubmed/28004885 http://dx.doi.org/10.1111/1751-7915.12468 Text en © 2016 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Elbehery, Ali H. A. Leak, David J. Siam, Rania Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool |
title | Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool |
title_full | Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool |
title_fullStr | Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool |
title_full_unstemmed | Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool |
title_short | Novel thermostable antibiotic resistance enzymes from the Atlantis II Deep Red Sea brine pool |
title_sort | novel thermostable antibiotic resistance enzymes from the atlantis ii deep red sea brine pool |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270753/ https://www.ncbi.nlm.nih.gov/pubmed/28004885 http://dx.doi.org/10.1111/1751-7915.12468 |
work_keys_str_mv | AT elbeheryaliha novelthermostableantibioticresistanceenzymesfromtheatlantisiideepredseabrinepool AT leakdavidj novelthermostableantibioticresistanceenzymesfromtheatlantisiideepredseabrinepool AT siamrania novelthermostableantibioticresistanceenzymesfromtheatlantisiideepredseabrinepool |