Polyester Biosynthesis Characteristics of Pseudomonas citronellolis Grown on Various Carbon Sources, Including 3-Methyl-Branched Substrates

Author:

Choi Mun Hwan1,Yoon Sung Chul1

Affiliation:

1. Biomacromolecules Research Laboratory, Department of Microbiology, Gyeongsang National University, Chinju 660-701, Republic of Korea

Abstract

Forty-two different carbon sources were tested for the polyester synthesis of a citronellol-utilizing bacterium, Pseudomonas citronellolis (ATCC 13674). These included linear C 2 to C 10 monocarboxylic acids, C 3 to C 10 dicarboxylic acids, saccharides, α,ω-diols, hydrocarbons, and 3-methyl-branched substrates such as 3,7-dimethyl-6-octen-1-ol (citronellol), 3-methyl- n -valerate, 3-methyl-1-butanol, and 3-methyladipate. Isolated polymers were characterized by gas chromatography, infrared spectroscopy, 1 H- or 13 C-nuclear magnetic resonance spectroscopy, 1 H- 13 C heteronuclear correlation spectroscopy ( 1 H- 13 C COSY), 1 H- 1 H homonuclear COSY, and differential scanning calorimetry. Polyesters from nine monocarboxylic acids and two related carbon sources could be metabolically divided into three groups. The first group of C 2 to C 4 carbon sources resulted in copolyesters composed of 61 to 70 mol% 3-hydroxydecanoate, 23 to 33 mol% 3-hydroxyoctanoate, 3.6 to 9.0 mol% 3-hydroxy-5- cis -dodecenoate, and 1.8 to 2.6 mol% 3-hydroxy-7- cis -tetradecenoate. Carbon sources in group II (C 7 to C 10 ) produced copolyesters composed of 3-hydroxyacid monomer units with the same number of carbon atoms as the substrate (major constituent) and monomer units with either two less or two more carbons. Negligible amounts of 3-hydroxy-5- cis -dodecenoate and 3-hydroxy-7- cis -tetradecenoate were detected in copolyesters from this group. Copolyesters from group III (C 5 and C 6 ) had a monomer unit distribution that could be said to be between those of groups I and II. In addition, a novel copolyester, poly(3-hydroxy-7-methyl-6-octenoate-co-3-hydroxy-5-methylhexanoate), was synthesized when grown on citronellol. The 1 H- 13 C heteronuclear COSY spectrum for monomer unit II revealed that both methylene and isopropyl groups, proximately connected in series to a single chiral center, had magnetically diastereotopic natures.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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