Methanol-induced chain termination in poly(3-hydroxybutyrate) biopolymers: Molecular weight control

被引:5
作者
Ashby, Richard D. [1 ]
Solaiman, Daniel K. Y. [1 ]
Strahan, Gary D. [1 ]
Levine, Alex C. [2 ]
Nomura, Christopher T. [2 ]
机构
[1] Agr Res Serv, Eastern Reg Res Ctr, USDA, Wyndmoor, PA 19038 USA
[2] SUNY Coll Environm Sci & Forestry, Dept Chem, Syracuse, NY 13210 USA
基金
美国国家科学基金会;
关键词
Poly(3-hydroxybutyrate); Methanol; Methoxy end-capping; Molecular weight control; CO-PRODUCT STREAM; PSEUDOMONAS-OLEOVORANS; LENGTH POLY(HYDROXYALKANOATES); POLYHYDROXYALKANOATES PHAS; CRUDE GLYCEROL; WASTE GLYCEROL; BIOSYNTHESIS; POLYESTERS; ACID; POLY(BETA-HYDROXYALKANOATES);
D O I
10.1016/j.ijbiomac.2014.12.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
A systematic study was performed to demonstrate the impact of methanol (MeOH) on poly(3-hydroxybutyrate) (PHB) synthesis and molecular weight (MW). Glycerine was used as the primary carbon source with varying concentrations of MeOH. Methanol retarded but did not completely inhibit growth and PHB production in Pseudomonas oleovorans. Proton NMR analysis revealed that the PHB polymers were end-capped with methoxy chemical groups causing MW reductions. The MW decreases were contingent upon the initial MeOH media concentration and the duration of the fermentations. The largest impact occurred at an initial MeOH concentration of 0.10% (w/v) where the number average molecular weights (M-n) decreased by 39%, 55%, and 72% in the 48, 72 and 96h cultures, respectively. Diffusion ordered NMR spectroscopy revealed a diffusivity (D) increase in the smaller molecular weight polymers with the PHB synthesized in the presence of 0.85% MeOH (72 h post-inoculation) having a D value of 0.66 x 10(-10) m(2)/s. Diffusivity increases indicate a reduction in hydrodynamic radii (R-hz) consistent with shorter chain-lengths. Crude glycerine from the biodiesel production process has been used as an inexpensive fermentation feedstock for polyhydroxyalkanoate (PHA) synthesis but its composition is facility-dependent. This information will be vital to tailor PHA properties to specific applications. Published by Elsevier B.V.
引用
收藏
页码:195 / 201
页数:7
相关论文
共 49 条
[1]
The application of biotechnological methods for the synthesis of biodiesel [J].
Adamczak, Marek ;
Bornscheuer, Uwe T. ;
Bednarski, Wtodzimierz .
EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, 2009, 111 (08) :800-813
[2]
Alper G.A., 1986, VISKOSITAT BINARER C, P1
[3]
Sophorolipid biosynthesis from a biodiesel co-product stream [J].
Ashby, RD ;
Nuñez, A ;
Solaiman, DKY ;
Foglia, TA .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 2005, 82 (09) :625-630
[4]
Synthesis of short-/medium-chain-length poly(hydroxyalkanoate) blends by mixed culture fermentation of glycerol [J].
Ashby, RD ;
Solaiman, DKY ;
Foglia, TA .
BIOMACROMOLECULES, 2005, 6 (04) :2106-2112
[5]
Bacterial poly(hydroxyalkanoate) polymer production from the biodiesel co-product stream [J].
Ashby, RD ;
Solaiman, DKY ;
Foglia, TA .
JOURNAL OF POLYMERS AND THE ENVIRONMENT, 2004, 12 (03) :105-112
[6]
Poly(ethylene glycol)-mediated molar mass control of short-chain- and medium-chain-length poly(hydroxyalkanoates) from Pseudomonas oleovorans [J].
Ashby, RD ;
Solaiman, DKY ;
Foglia, TA .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2002, 60 (1-2) :154-159
[7]
Ashby RD, 1999, BIOTECHNOL BIOENG, V62, P106, DOI 10.1002/(SICI)1097-0290(19990105)62:1<106::AID-BIT12>3.0.CO
[8]
2-X
[9]
Glucose/lipid mixed substrates as a means of controlling the properties of medium chain length poly(hydroxyalkanoates) [J].
Ashby, RD ;
Solaiman, DKY ;
Foglia, TA ;
Liu, CK .
BIOMACROMOLECULES, 2001, 2 (01) :211-216
[10]
Glycerine and levulinic acid: Renewable co-substrates for the fermentative synthesis of short-chain poly(hydroxyalkanoate) biopolymers [J].
Ashby, Richard D. ;
Solaiman, Daniel K. Y. ;
Strahan, Gary D. ;
Zhu, Chengjun ;
Tappel, Ryan C. ;
Nomura, Christopher T. .
BIORESOURCE TECHNOLOGY, 2012, 118 :272-280