Cargando…

Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis

Polyhydroxyalkanoates (PHA) are biodegradable polymers that are attractive materials for use in tissue engineering and medical device manufacturing. Ralstonia eutropha is regarded as the model organism for PHA biosynthesis. We examined the effects of PHA depolymerase (PhaZ) expression on PHA homeost...

Descripción completa

Detalles Bibliográficos
Autores principales: Brigham, Christopher J, Reimer, Esther N, Rha, ChoKyun, Sinskey, Anthony J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430594/
https://www.ncbi.nlm.nih.gov/pubmed/22537946
http://dx.doi.org/10.1186/2191-0855-2-26
_version_ 1782241958582812672
author Brigham, Christopher J
Reimer, Esther N
Rha, ChoKyun
Sinskey, Anthony J
author_facet Brigham, Christopher J
Reimer, Esther N
Rha, ChoKyun
Sinskey, Anthony J
author_sort Brigham, Christopher J
collection PubMed
description Polyhydroxyalkanoates (PHA) are biodegradable polymers that are attractive materials for use in tissue engineering and medical device manufacturing. Ralstonia eutropha is regarded as the model organism for PHA biosynthesis. We examined the effects of PHA depolymerase (PhaZ) expression on PHA homeostasis in R. eutropha strains. In order to analyze the impact of PhaZs on R. eutropha granule architecture, we performed electron microscopy on several phaZ knockout strains and the wild type strain grown under PHA production conditions. Analysis of the acquired micrographs was based on stereology: the ratio of granule area and cell area was determined, along with total granule count per full-size cell image. Cells bearing a phaZ2 knockout mutation alone or in conjunction with a phaZ1 mutation were found to have a high granule volume per cell volume and a higher granule count compared to wild type. A phaZ quadruple knockout strain appeared to have a low granule volume per cell volume and a low granule count per cell. Cells bearing a phaZ3 knockout were found to have a higher granule count than the wild type, whereas granule volume per cell volume was similar. Accordingly, we hypothesize that PhaZs have not only an impact on PHA degradation but also on the 3-dimensional granule architecture. Based on our data, PhaZ2 is postulated to affect granule density. This work increased our knowledge about PHA depolymerases in R. eutropha, including enzymes that had previously been uncharacterized.
format Online
Article
Text
id pubmed-3430594
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-34305942012-08-30 Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis Brigham, Christopher J Reimer, Esther N Rha, ChoKyun Sinskey, Anthony J AMB Express Original Article Polyhydroxyalkanoates (PHA) are biodegradable polymers that are attractive materials for use in tissue engineering and medical device manufacturing. Ralstonia eutropha is regarded as the model organism for PHA biosynthesis. We examined the effects of PHA depolymerase (PhaZ) expression on PHA homeostasis in R. eutropha strains. In order to analyze the impact of PhaZs on R. eutropha granule architecture, we performed electron microscopy on several phaZ knockout strains and the wild type strain grown under PHA production conditions. Analysis of the acquired micrographs was based on stereology: the ratio of granule area and cell area was determined, along with total granule count per full-size cell image. Cells bearing a phaZ2 knockout mutation alone or in conjunction with a phaZ1 mutation were found to have a high granule volume per cell volume and a higher granule count compared to wild type. A phaZ quadruple knockout strain appeared to have a low granule volume per cell volume and a low granule count per cell. Cells bearing a phaZ3 knockout were found to have a higher granule count than the wild type, whereas granule volume per cell volume was similar. Accordingly, we hypothesize that PhaZs have not only an impact on PHA degradation but also on the 3-dimensional granule architecture. Based on our data, PhaZ2 is postulated to affect granule density. This work increased our knowledge about PHA depolymerases in R. eutropha, including enzymes that had previously been uncharacterized. Springer 2012-04-26 /pmc/articles/PMC3430594/ /pubmed/22537946 http://dx.doi.org/10.1186/2191-0855-2-26 Text en Copyright ©2012 Brigham et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Brigham, Christopher J
Reimer, Esther N
Rha, ChoKyun
Sinskey, Anthony J
Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis
title Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis
title_full Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis
title_fullStr Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis
title_full_unstemmed Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis
title_short Examination of PHB Depolymerases in Ralstonia eutropha: Further Elucidation of the Roles of Enzymes in PHB Homeostasis
title_sort examination of phb depolymerases in ralstonia eutropha: further elucidation of the roles of enzymes in phb homeostasis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430594/
https://www.ncbi.nlm.nih.gov/pubmed/22537946
http://dx.doi.org/10.1186/2191-0855-2-26
work_keys_str_mv AT brighamchristopherj examinationofphbdepolymerasesinralstoniaeutrophafurtherelucidationoftherolesofenzymesinphbhomeostasis
AT reimeresthern examinationofphbdepolymerasesinralstoniaeutrophafurtherelucidationoftherolesofenzymesinphbhomeostasis
AT rhachokyun examinationofphbdepolymerasesinralstoniaeutrophafurtherelucidationoftherolesofenzymesinphbhomeostasis
AT sinskeyanthonyj examinationofphbdepolymerasesinralstoniaeutrophafurtherelucidationoftherolesofenzymesinphbhomeostasis