1986
DOI: 10.1021/ma00165a033
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Nuclear magnetic resonance studies on poly(β-hydroxybutyrate) and a copolyester of β-hydroxybutyrate and β-hydroxyvalerate isolated from Alcaligenes eutrophus H16

Abstract: Poly(/3-hydroxybutyrate) (PHB) and a copolyester of /3-hydroxybutyrate and /3-hydroxyvalerate are isolated from Alcaligenes eutrophus H16 grown in nitrogen-free culture media containing CHgCOONa and CHgCH2COONa as carbon sources. The chain dynamics of PHB (Mw = 420000) in chloroform are studied by 13C NMR measurement at 25 MHz. The carbon-13 spin-lattice relaxation times (TJ and nuclear Overhauser enhancements (NOE) indicate that the average correlation times (tc) for segmental motion of the PHB molecule are i… Show more

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Cited by 231 publications
(116 citation statements)
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“…The main bands and peaks of the FTIR and 1 H NMR spectra correspond to PHB, according to those found in the literature [42]. Furthermore, the chemical signals obtained in the present work agree with those obtained by [43] for a PHB produced by fermentation. These results together with the FT-IR analysis showed that strain SA8 was able to accumulate PHB using glycerol as a substrate.…”
Section: Discussionsupporting
confidence: 90%
“…The main bands and peaks of the FTIR and 1 H NMR spectra correspond to PHB, according to those found in the literature [42]. Furthermore, the chemical signals obtained in the present work agree with those obtained by [43] for a PHB produced by fermentation. These results together with the FT-IR analysis showed that strain SA8 was able to accumulate PHB using glycerol as a substrate.…”
Section: Discussionsupporting
confidence: 90%
“…The 13 C NMR analysis supported the results from the proton NMR analysis. The resonance of the monomers at 19.87 (9), 40.80 (7), 67.64 (8), and 169.26 (1) ppm were assigned by data comparison to 3HB according to the previous report (Doi et al, 1986), whereas the resonances at 22.10 (4), 38.65 (2) and 71.91 ppm were referred to 3HV. In contrast, 1 H NMR spectral analyses of the purified polymer from the recombinant yeast strain INVSc1/ PHA1 revealed the presence of 3, 2 and 1 protons at chemical shifts 1.2, 2.4-2.6 and 5.3, respectively (Fig.…”
Section: Pha Analysismentioning
confidence: 99%
“…Analytical methods. PHB was extracted from cells by the method of Doi et al (11) and converted to crotonic acid as described by Law and Slepecky (24). Crotonic acid was quantified by HPLC on a Polypore H column (4.6 mm by 250 mm; Brownlee, Kontron, Eching, Germany) in accordance with the procedure of Karr et al (20).…”
Section: Microscopy Of Cell Suspensions and Stained Cellsmentioning
confidence: 99%