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Highlights • THM-GC was applied to monitor the change in copolymer composition of film samples during soil burial test. • 3 HHx moieties in the polymer chains were preferentially biodegraded owing to their low crystallinity. • Local variation in the degree of biodegradation using only 30 μg of P(3HB-co-3HHx) film sample. Abstract Soil burial biodegradation behavior of poly(3-hydroxybutyrate- co -3-hydroxyhexanoate) [P(3HB- co -3HHx)] was studied based on its copolymer composition determined by thermally assisted hydrolysis and methylation-gas chromatography (THM-GC). The change in copolymer composition of P(3HB- co -3HHx) film samples during soil burial degradation test was monitored in detail by THM-GC. As a result, the copolymer compositions of 3HB units gradually increased, while those of 3HHx units decreased with soil burial time, almost correlating with recovery weight. Based on these results, the biodegradation mechanism of P(3HB- co -3HHx) was elucidated with considering the influence of the crystallinity on the biodegradability. Furthermore, local differences in biodegradability of a given P(3HB- co -3HHx) film after soil burial test were also successfully evaluated from the copolymer compositions obtained by THM-GC. [ABSTRACT FROM AUTHOR]

Thermally assisted hydrolysis and methylation-gas chromatography (THM-GC) in the presence of an organic alkali was validated for the compositional analysis of poly(3-hydroxybutyrate- co -3-hydroxyhexanoate) [P(3HB- co -3HHx)] accumulated in whole bacterial cells. Recombinant Cupriavidus necator Re2058/pCB113 was grown in a batch fermentation with different concentration of palm oil and fructose in order to control the molar fraction of 3HHx in P(3HB- co -3HHx) produced in the cells. Trace amounts (30 μg) of freeze-dried cells were directly subjected to THM-GC in the presence of tetramethylammonium hydroxide (TMAH) at 400 °C. The obtained chromatograms clearly showed nine characteristic peaks, attributed to the THM products from 3HB and 3HHx units in the polymer chains, without any appreciable interference by the bacterial matrix components. Based on these peak intensities, the copolymer compositions were determined rapidly without using any cumbersome and lengthy sample pretreatment as in conventional GC method. Moreover, the compositions thus obtained were strongly correlated with those by NMR and conventional GC involving solvent extraction. [ABSTRACT FROM AUTHOR]