1989
DOI: 10.1021/ma00193a018
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The biosynthesis and characterization of poly(β-hydroxyalkanoates) produced by Pseudomonas oleovorans

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Cited by 306 publications
(218 citation statements)
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“…Similar results were reported previously, showing that PHA produced by P. oleovorans from hexanoate and heptanoate did not have a clear melting point, whereas PHA produced from longer-chain alkanoates did (1,11,28).…”
Section: Discussionsupporting
confidence: 90%
See 1 more Smart Citation
“…Similar results were reported previously, showing that PHA produced by P. oleovorans from hexanoate and heptanoate did not have a clear melting point, whereas PHA produced from longer-chain alkanoates did (1,11,28).…”
Section: Discussionsupporting
confidence: 90%
“…Thus, PHAs from JMU194(pBTC2, pET901) containing mostly propyl pendant groups showed higher PD than PHAs from JMU194(pBTC2, pCK01) containing mostly valeryl pendant groups. Similar results have been reported by Fuller and coworkers, who showed that the PD for PHA synthesized by P. oleovorans when grown on hexanaote and heptanoate was approximately twice as large as the PD for PHA which was produced when using octanoate and other longer-chain-length alkanoates (11).…”
Section: Discussionsupporting
confidence: 89%
“…These species include P. marginalis (DSM 50276), P. mendocina (ATCC 25411), P. putida GPo1 (ATCC 29347), and P. oleovorans (ATCC 8062) when n-alkanoates and 1,3-butanediol were provided as carbon sources [56,78,82]. For most of these Pseudomonad species, 3-hydroxybutyrate (3HB) is typically incorporated as a minor constituent in scl-mcl-PHA (between less than 1 mol% and 7.8 mol%) [78,82]. An exception is P. oleovorans (ATCC 8062) where its cultivation on 4-hydroxyhexanoic acid resulted in a copolymer predominated by 3HB (92.4 mol%) [56].…”
Section: Gram-negative Bacteriamentioning
confidence: 99%
“…It has been reported that poly(3-hydroxybutyrate-co-4-hydroxybutyrate) had a much faster degradation rate than homopolymer PHB (178). mcl-PHAs are rubbery and flexible materials with low crystallinity and can be used in a wide range of applications which cannot be fulfilled by PHB and other scl-PHAs (223) but these physical properties of mcl-PHAs are considered unsuitable for applications due to their low T m and T g (226,227). In contrast to PHB and P(HB-HV), mcl-PHAs have a much lower level of crystallinity and are more elastic (226, 228) but not strong enough for applications.…”
Section: Physical Propertiesmentioning
confidence: 99%