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Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis
PHA synthases (PhaC) are grouped into four classes based on the kinetics and mechanisms of reaction. The grouping of PhaC enzymes into four classes is dependent on substrate specificity, according to the preference in forming short-chain-length (scl) or medium-chain-length (mcl) polymers: Class I, C...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403647/ https://www.ncbi.nlm.nih.gov/pubmed/30960835 http://dx.doi.org/10.3390/polym10080910 |
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author | Mezzolla, Valeria D’Urso, Oscar Fernando Poltronieri, Palmiro |
author_facet | Mezzolla, Valeria D’Urso, Oscar Fernando Poltronieri, Palmiro |
author_sort | Mezzolla, Valeria |
collection | PubMed |
description | PHA synthases (PhaC) are grouped into four classes based on the kinetics and mechanisms of reaction. The grouping of PhaC enzymes into four classes is dependent on substrate specificity, according to the preference in forming short-chain-length (scl) or medium-chain-length (mcl) polymers: Class I, Class III and Class IV produce scl-PHAs depending on propionate, butyrate, valerate and hexanoate precursors, while Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors. PHA synthases of Class I, in particular PhaC(Cs) from Chromobacterium USM2 and PhaC(Cn)/RePhaC1 from Cupriavidus necator/Ralstonia eutropha, have been analysed and the crystal structures of the C-domains have been determined. PhaC(Cn)/RePhaC1 was also studied by X-ray absorption fine-structure (XAFS) analysis. Models have been proposed for dimerization, catalysis mechanism, substrate recognition and affinity, product formation, and product egress route. The assays based on amino acid substitution by mutagenesis have been useful to validate the hypothesis on the role of amino acids in catalysis and in accommodation of bulky substrates, and for the synthesis of PHB copolymers and medium-chain-length PHA polymers with optimized chemical properties. |
format | Online Article Text |
id | pubmed-6403647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64036472019-04-02 Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis Mezzolla, Valeria D’Urso, Oscar Fernando Poltronieri, Palmiro Polymers (Basel) Review PHA synthases (PhaC) are grouped into four classes based on the kinetics and mechanisms of reaction. The grouping of PhaC enzymes into four classes is dependent on substrate specificity, according to the preference in forming short-chain-length (scl) or medium-chain-length (mcl) polymers: Class I, Class III and Class IV produce scl-PHAs depending on propionate, butyrate, valerate and hexanoate precursors, while Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors. PHA synthases of Class I, in particular PhaC(Cs) from Chromobacterium USM2 and PhaC(Cn)/RePhaC1 from Cupriavidus necator/Ralstonia eutropha, have been analysed and the crystal structures of the C-domains have been determined. PhaC(Cn)/RePhaC1 was also studied by X-ray absorption fine-structure (XAFS) analysis. Models have been proposed for dimerization, catalysis mechanism, substrate recognition and affinity, product formation, and product egress route. The assays based on amino acid substitution by mutagenesis have been useful to validate the hypothesis on the role of amino acids in catalysis and in accommodation of bulky substrates, and for the synthesis of PHB copolymers and medium-chain-length PHA polymers with optimized chemical properties. MDPI 2018-08-13 /pmc/articles/PMC6403647/ /pubmed/30960835 http://dx.doi.org/10.3390/polym10080910 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mezzolla, Valeria D’Urso, Oscar Fernando Poltronieri, Palmiro Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis |
title | Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis |
title_full | Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis |
title_fullStr | Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis |
title_full_unstemmed | Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis |
title_short | Role of PhaC Type I and Type II Enzymes during PHA Biosynthesis |
title_sort | role of phac type i and type ii enzymes during pha biosynthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403647/ https://www.ncbi.nlm.nih.gov/pubmed/30960835 http://dx.doi.org/10.3390/polym10080910 |
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