Literature DB >> 12074088

The synthesis of short- and medium-chain-length poly(hydroxyalkanoate) mixtures from glucose- or alkanoic acid-grown Pseudomonas oleovorans.

R D Ashby1, D K Y Solaiman, T A Foglia.   

Abstract

Pseudomonas oleovorans NRRL B-778 accumulated mixtures of poly-3-hydroxybutyrate (PHB) and medium-chain-length poly(hydroxyalkanoates) (mcl-PHAs) when grown on glucose, octanoic acid or oleic acid, whereas growth on nonanoic acid or undecanoic acid resulted in copolymers of poly-3-hydroxybutyrate-co-3-hydroxyvalerate (PHB-co-HV). Acetone fractionation verified the presence of PHB/mcl-PHA mixtures. The acetone-insoluble (AIS) fractions of the polymers derived from glucose (PHA-glucose), octanoic acid (PHA-octanoic) and oleic acid (PHA-oleic) were exclusively PHB while the acetone-soluble (AS) fractions contained mcl-PHA composed of differing ratios of 3-hydroxy-acid monomer units, which ranged in chain length from 6 to 14 carbon atoms. In contrast, both the AIS and AS fractions from the polymers derived from nonanoic acid (PHA-nonanoic) and undecanoic acid (PHA-undecanoic) were composed of comparable ratios of 3-hydroxybutyrate (3HB) and 3-hydroxyvalerate (3HV). The unfractionated PHA-glucose, PHA-octanoic and PHA-oleic polymers had melting temperatures (Tm) between 177 and 179 degrees C, enthalpies of fusion (AHf) of 20 cal/g and glasstransition temperatures (Tg) of 3-4 degrees C. This was due to the large PHB content in the polymer mixtures. On the other hand, the PHA-nonanoic and PHA-undecanoic polymers had thermal properties that supported their copolymer nature. In both cases, the Tm values were 161 degrees C, deltaHf values were 7 cal/g and Tg values were - 3 degrees C.

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Year:  2002        PMID: 12074088     DOI: 10.1038/sj.jim.7000231

Source DB:  PubMed          Journal:  J Ind Microbiol Biotechnol        ISSN: 1367-5435            Impact factor:   3.346


  6 in total

1.  Genetic characterization of the poly(hydroxyalkanoate) synthases of various Pseudomonas oleovorans strains.

Authors:  Daniel K Y Solaiman; Richard D Ashby
Journal:  Curr Microbiol       Date:  2005-06-13       Impact factor: 2.188

Review 2.  Challenges and Opportunities for Customizing Polyhydroxyalkanoates.

Authors:  Mamtesh Singh; Prasun Kumar; Subhasree Ray; Vipin C Kalia
Journal:  Indian J Microbiol       Date:  2015-04-14       Impact factor: 2.461

3.  Pseudomonas sp. as a Source of Medium Chain Length Polyhydroxyalkanoates for Controlled Drug Delivery: Perspective.

Authors:  Sujatha Kabilan; Mahalakshmi Ayyasamy; Sridhar Jayavel; Gunasekaran Paramasamy
Journal:  Int J Microbiol       Date:  2012-02-08

4.  Poly(3-hydroxybutyrate) hyperproduction by a global nitrogen regulator NtrB mutant strain of Paracoccus denitrificans PD1222.

Authors:  Alfonso Olaya-Abril; Víctor M Luque-Almagro; Isabel Manso; Andrew J Gates; Conrado Moreno-Vivián; David J Richardson; María Dolores Roldán
Journal:  FEMS Microbiol Lett       Date:  2018-01-01       Impact factor: 2.742

Review 5.  Microbial-Derived Polyhydroxyalkanoate-Based Scaffolds for Bone Tissue Engineering: Biosynthesis, Properties, and Perspectives.

Authors:  Jian Li; Xu Zhang; Anjaneyulu Udduttula; Zhi Shan Fan; Jian Hai Chen; Antonia RuJia Sun; Peng Zhang
Journal:  Front Bioeng Biotechnol       Date:  2021-12-21

6.  Pseudomonas pseudoalcaligenes CECT5344, a cyanide-degrading bacterium with by-product (polyhydroxyalkanoates) formation capacity.

Authors:  Isabel Manso Cobos; María Isabel Ibáñez García; Fernando de la Peña Moreno; Lara Paloma Sáez Melero; Víctor Manuel Luque-Almagro; Francisco Castillo Rodríguez; María Dolores Roldán Ruiz; María Auxiliadora Prieto Jiménez; Conrado Moreno Vivián
Journal:  Microb Cell Fact       Date:  2015-06-10       Impact factor: 5.328

  6 in total

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