Production of lovastatin by Aspergillus terreus:: effects of the C:N ratio and the principal nutrients on growth and metabolite production

被引:158
作者
López, JLC [1 ]
Pérez, JAS
Sevilla, JMF
Fernández, FGA
Grima, EM
Chisti, Y
机构
[1] Univ Almeria, Dept Chem Engn, Almeria 04120, Spain
[2] Massey Univ, Inst Technol & Engn, Palmerston North, New Zealand
关键词
lovastatin; mevinolin fermentation;
D O I
10.1016/S0141-0229(03)00130-3
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 lovastatin and microbial biomass by Aspergillus terreus ATCC 20542 were influenced by the type of the carbon source (lactose, glycerol, and fructose) and the nitrogen source (yeast extract, corn steep liquor, and soybean meal) used and the C:N mass ratio in the medium. Use of a slowly metabolized carbon source (lactose) in combination with either soybean meal or yeast extract under N-limited conditions gave the highest titers and specific productivity (similar to0.1 mg g(-1) h(-1)) of lovastatin. The maximum value of the lovastatin yield coefficient on biomass was similar to30 mg g(-1) using the lactose/soybean meal and lactose/yeast extract media. The optimal initial C:N mass ratio for attaining high productivity of lovastatin was similar to40. The behavior of the fermentation was not affected by the method of inoculation (fungal spores or hyphae) used, but the use of spores gave a more consistent inoculum in the different runs. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:270 / 277
页数:8
相关论文
共 19 条
[1]   MEVINOLIN - A HIGHLY POTENT COMPETITIVE INHIBITOR OF HYDROXYMETHYLGLUTARYL-COENZYME-A REDUCTASE AND A CHOLESTEROL-LOWERING AGENT [J].
ALBERTS, AW ;
CHEN, J ;
KURON, G ;
HUNT, V ;
HUFF, J ;
HOFFMAN, C ;
ROTHROCK, J ;
LOPEZ, M ;
JOSHUA, H ;
HARRIS, E ;
PATCHETT, A ;
MONAGHAN, R ;
CURRIE, S ;
STAPLEY, E ;
ALBERSSCHONBERG, G ;
HENSENS, O ;
HIRSHFIELD, J ;
HOOGSTEEN, K ;
LIESCH, J ;
SPRINGER, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :3957-3961
[2]   LOVASTATIN AND SIMVASTATIN - INHIBITORS OF HMG COA REDUCTASE AND CHOLESTEROL-BIOSYNTHESIS [J].
ALBERTS, AW .
CARDIOLOGY, 1990, 77 :14-21
[3]  
[Anonymous], 1989, NOVEL MICROB PROD ME, DOI DOI 10.4103/0250-474X.49087
[4]  
Daborah R. A., 1992, British Patent GB, Patent No. 2255974
[5]   COMPETITIVE INHIBITION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE BY ML-236A AND ML-236B FUNGAL METABOLITES, HAVING HYPOCHOLESTEROLEMIC ACTIVITY [J].
ENDO, A ;
KURODA, M ;
TANZAWA, K .
FEBS LETTERS, 1976, 72 (02) :323-326
[6]   ML-236A, ML-236B, AND ML-236C, NEW INHIBITORS OF CHOLESTEROGENESIS PRODUCED BY PENICILLIUM CITRINUM [J].
ENDO, A ;
KURODA, M ;
TSUJITA, Y .
JOURNAL OF ANTIBIOTICS, 1976, 29 (12) :1346-1348
[7]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF MEVINOLIN AS MEVINOLINIC ACID IN FERMENTATION BROTHS [J].
FRIEDRICH, J ;
ZUZEK, M ;
BENCINA, M ;
CIMERMAN, A ;
STRANCAR, A ;
RADEZ, I .
JOURNAL OF CHROMATOGRAPHY A, 1995, 704 (02) :363-367
[8]   Fermentation optimization for the production of poly(β-hydroxybutyric acid) microbial thermoplastic [J].
Grothe, E ;
Moo-Young, M ;
Chisti, Y .
ENZYME AND MICROBIAL TECHNOLOGY, 1999, 25 (1-2) :132-141
[9]   Lovastatin biosynthesis by Aspergillus terreus in a chemically defined medium [J].
Hajjaj, H ;
Niederberger, P ;
Duboc, P .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (06) :2596-2602
[10]   Secondary metabolites of the fungus Monascus: A review [J].
Juzlova, P ;
Martinkova, L ;
Kren, V .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1996, 16 (03) :163-170