Agro-industrial oily wastes as substrates for PHA production by the new strain Pseudomonas aeruginosa NCIB 40045:: Effect of culture conditions

被引:111
作者
Fernández, D
Rodríguez, E
Bassas, M
Viñas, M
Solanas, AM
Llorens, J
Marqués, AM
Manresa, A
机构
[1] Univ Barcelona, Fac Farm, Microbiol Lab, E-08028 Barcelona, Spain
[2] Univ Barcelona, Fac Biol, Dept Microbiol, E-08028 Barcelona, Spain
[3] Univ Barcelona, Dept Ingn Quim, E-08028 Barcelona, Spain
关键词
PHA; waste-free fatty acids; low aeration rates;
D O I
10.1016/j.bej.2005.04.022
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Production of poly(3-hydroxyalkaonates) (PHA) by Pseudomonas aeruginosa 42A2 from agro-industrial oily wastes was studied. PHA accumulation, throughout the cell cycle, was observed as intracellular accumulation associated to polyphosphate granules. A 54.6% PHA accumulation was obtained-when technical oleic acid (TOA) was used as carbon source. Molecular weight of the polymer was 54.7 Da. The polymer was amorphous, with glass transition at -47.5 degrees C and thermal degradation at 293 degrees C. PHA production and monomer composition were affected by K-La and temperature. The most relevant characteristic of the polymer produced at low aeration rates (K-La, 0.06 s(-1)) were the unusual C-14:2 (13%) and the increase Of C-12:1 (42.2%). The highest amount of unsaturated monomers was found in the polymer produced at 18 degrees C (64.4%). PHA accumulation ranged between 66.1% when waste-free fatty acids from soybean oil (WFFA) were used as carbon substrate, 29.4% when waste frying oil (WFO) was used and 16.8% when glucose was used. Depending on the substrate supplied a wide range of components was observed. Major saturated or unsaturated components of the polymer found were C-10:0, C-12:0 and C-8:0 or C-12:1 and C-14:1, respectively. When glucose was used as carbon substrate C-9:0, C-11:0 and C-16:0 were found. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 167
页数:9
相关论文
共 50 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Lipid storage compounds in marine bacteria [J].
Alvarez, HM ;
Pucci, OH ;
Steinbuchel, A .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1997, 47 (02) :132-139
[3]  
ASBHY R, 2002, APPL MICROBIOL BIOT, V60, P154
[4]   Biosynthesis and structural characterization of medium-chain-length poly(3-hydroxyalkanoates) produced by Pseudomonas aeruginosa from fatty acids [J].
Ballistreri, A ;
Giuffrida, M ;
Guglielmino, SPP ;
Carnazza, S ;
Ferreri, A ;
Impallomeni, G .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2001, 29 (02) :107-114
[5]   DEGRADATION AND APPLICATIONS OF POLYHYDROXYALKANOATES [J].
BRANDL, H ;
BACHOFEN, R ;
MAYER, J ;
WINTERMANTEL, E .
CANADIAN JOURNAL OF MICROBIOLOGY, 1995, 41 :143-153
[6]   Economic considerations in the production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) by bacterial fermentation [J].
Choi, J ;
Lee, SY .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2000, 53 (06) :646-649
[7]  
Christie W.W., 2003, Lipid Analysis, V3rd, P205
[8]   The microbial production of poly(hydroxyalkanoates) from tallow [J].
Cromwick, AM ;
Foglia, T ;
Lenz, RW .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1996, 46 (5-6) :464-469
[9]   Biotransformation of oleic acid into (E)-10-hydroxy-8-octadecenoic acid and (E)-7,10-dihydroxy-8-octadecenoic acid by Pseudomonas sp 42A2 in an immobilized system [J].
Culleré, J ;
Durany, O ;
Busquets, M ;
Manresa, A .
BIOTECHNOLOGY LETTERS, 2001, 23 (03) :215-219
[10]   16S ribosomal DNA sequence analysis of a large collection of environmental and clinical unidentifiable bacterial isolates [J].
Drancourt, M ;
Bollet, C ;
Carlioz, A ;
Martelin, R ;
Gayral, JP ;
Raoult, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (10) :3623-3630