Differential sensitivity of polyhydroxyalkanoate producing bacteria to fermentation inhibitors and comparison of polyhydroxybutyrate production from Burkholderia cepacia and Pseudomonas pseudoflava

被引:31
作者
Dietrich D. [1 ]
Illman B. [1 ]
Crooks C. [1 ]
机构
[1] USDA Forest Service, Forest Products Laboratory, Madison, WI 53726, One Gifford Pinchot Drive
关键词
Bioconversion; Fermentation inhibitors; Polyhydroxyalkanoate;
D O I
10.1186/1756-0500-6-219
中图分类号
学科分类号
摘要
Background: The aim of this study is determine the relative sensitivity of a panel of seven polyhydroxyalkanoate producing bacteria to a panel of seven lignocellulosic-derived fermentation inhibitors representing aliphatic acids, furans and phenolics. A further aim was to measure the polyhydroxybutyrate production of select organisms on lignocellulosic-derived monosaccharides arabinose, xylose, glucose and mannose. Findings. We examined the sensitivity of seven polyhydroxyalkanoate producing bacteria: Azohydromonas lata, Bacillus megaterium, Bacillus cereus, Burkholderia cepacia, Pseudomonas olevorans, Pseudomonas pseudoflava and Ralstonia eutropha, against seven fermentation inhibitors produced by the saccharification of lignocellulose: acetic acid, levulinic acid, coumaric acid, ferulic acid, syringaldehyde, furfural, and hyroxymethyfurfural. There was significant variation in the sensitivity of these microbes to representative phenolics ranging from 0.25-1.5 g/L coumaric and ferulic acid and between 0.5-6.0 g/L syringaldehyde. Inhibition ranged from 0.37-4 g/L and 0.75-6 g/L with acetic acid and levulinic acid, respectively. B. cepacia and P. pseudoflava were selected for further analysis of polyhydroxyalkanoate production. Conclusions: We find significant differences in sensitivity to the fermentation inhibitors tested and find these variations to be over a relevant concentration range given the concentrations of inhibitors typically found in lignocellulosic hydrolysates. Of the seven bacteria tested, B. cepacia demonstrated the greatest inhibitor tolerance. Similarly, of two organisms examined for polyhydroxybutyrate production, B. cepacia was notably more efficient when fermenting pentose substrates. © 2013 Dietrich et al.; licensee BioMed Central Ltd.
引用
收藏
相关论文
共 12 条
[1]  
Brandl H., Gross R.A., Lenz R.W., Fuller R.C., Plastics from bacteria and for bacteria: Poly(β-hydroxyalkanoates) as natural, biocompatible, and biodegradable polyesters, Adv Biochem Eng Biotechnol, 41, pp. 77-93, (1990)
[2]  
Ramsay B.A., Lomaliza K., Chavarie C., Dube B., Bataille P., Ramsay J.A., Production of poly-(β-hydroxybutyric-co-β-hydroxyvaleric) acids, Applied and Environmental Microbiology, 56, 7, pp. 2093-2098, (1990)
[3]  
Palmqvist E., Hahn-Hagerdal B., Fermentation of lignocellulosic hydrolysates. I: Inhibition and detoxification, Bioresource Technology, 74, 1, pp. 17-24, (2000)
[4]  
Palmqvist E., Hahn-Hagerdal B., Fermentation of lignocellulosic hydrolysates. II: Inhibitors and mechanisms of inhibition, Bioresource Technology, 74, 1, pp. 25-33, (2000)
[5]  
Choi J., Lee S.Y., Factors affecting the economics of polyhydroxyalkanoate production by bacterial fermentation, Applied Microbiology and Biotechnology, 51, 1, pp. 13-21, (1999)
[6]  
Jimenez J.I., Minambres B., Garcia J.L., Diaz E., Genomic analysis of the aromatic catabolic pathways from Pseudomonas putida KT2440, Environmental Microbiology, 4, 12, pp. 824-841, (2002)
[7]  
Koopman F., Wierckx N., De Winde J.H., Ruijssenaars H.J., Identifcation and characterization of the furfural and 5-(hydroxymethyl) furfural degradation pathways of Cupriavidus basilensis HMF14, Proc Natl Acad Sci USA, 107, pp. 4919-4924, (2010)
[8]  
Pan W., Perrotta J.A., Stipanovic A.J., Nomura C.T., Nakas J.P., Production of polyhydroxyalkanoates by Burkholderia cepacia ATCC 17759 using a detoxified sugar maple hemicellulosic hydrolysate, J Ind Microbiol Biotechnol, 39, pp. 459-469, (2012)
[9]  
Keenan T.M., Tanenbaum S.W., Stipanovic A.J., Nakas J.P., Production and characterization of poly-β-hydroxyalkanoate copolymers from Burkholderia cepacia utilizing xylose and levulinic acid, Biotechnology Progress, 20, 6, pp. 1697-1704, (2004)
[10]  
Wiegand I., Hilpert K., Hancock R.E.W., Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances, Nature Protocols, 3, 2, pp. 163-175, (2008)