Effects of divalent metal cations on lovastatin biosynthesis from Aspergillus terreus in chemically defined medium

被引:20
作者
Jia, Zhihua [2 ]
Zhang, Xiaoli [1 ]
Zhao, Yaling [1 ]
Cao, Xuejun [2 ]
机构
[1] NW Univ Xian, Coll Chem Engn, Xian 710069, Peoples R China
[2] E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
关键词
Aspergillus terreus; Lovastatin; Monacolin J; Divalent metal ions; Biosynthesis; MORPHOLOGY; MEVINOLIN; COENZYME; NIGER;
D O I
10.1007/s11274-009-0007-5
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
Effects of six divalent metal cations: Fe2+, Ca2+, Zn2+, Mg2+, Cu(2+)and Mn2+ on fungal cell growth and lovastatin biosynthesis were investigated by submerged cultivation of Aspergillus terreus in a modified chemically defined medium. The influences of different initial concentrations of the above six metal cations were also examined at 1, 2, and 5 mM, respectively. Cu2+ apparently inhibited the cell growth, but had no influence on biosynthesis of lovastatin. All of Fe2+, Ca2+, Zn2+, Mg2+ and Mn2+ promoted the cell growth and lovastatin biosynthesis in different extents. The highest biomass of 13.8 +/- A 0.5 g l(-1) and specific lovastatin titres of 49.2 +/- A 1.4 mg gDCW(-1) were obtained at the level of 2 and 5 mM in the presence of Zn2+, respectively. The values were improved double and 14.4-fold. Excess Zn2+ inhibited the cell growth, but enhanced lovastatin biosynthesis with an increment of 17.6 mg l(-1) per mM. The interactions of all metal cations slightly inhibited the lovastatin production comparing with the existence of Zn2+, Fe2+ and Mg2+ solely, yet remarkably improved the cell growth. These results suggest that the divalent metal ions Zn2+ or Fe2+ influence the production by regulating the action of key enzymes such as LovD or LovF in lovastatin biosynthesis.
引用
收藏
页码:1235 / 1241
页数:7
相关论文
共 22 条
[11]   A rapid technique for screening of lovastatin-producing strains of Aspergillus terreus by agar plug and Neurospora crassa bioassay [J].
Kumar, MS ;
Kumar, PM ;
Sarnaik, HM ;
Sadhukhan, AK .
JOURNAL OF MICROBIOLOGICAL METHODS, 2000, 40 (01) :99-104
[12]   The influence of culturing environments on lovastatin production by Aspergillus terreus in submerged cultures [J].
Lai, LST ;
Tsai, TH ;
Wang, TC ;
Cheng, TY .
ENZYME AND MICROBIAL TECHNOLOGY, 2005, 36 (5-6) :737-748
[13]   The influence of medium design on lovastatin production and pellet formation with a high-producing mutant of Aspergillus terreus in submerged cultures [J].
Lai, LST ;
Pan, CC ;
Tzeng, BK .
PROCESS BIOCHEMISTRY, 2003, 38 (09) :1317-1326
[14]   Production of lovastatin by Aspergillus terreus:: effects of the C:N ratio and the principal nutrients on growth and metabolite production [J].
López, JLC ;
Pérez, JAS ;
Sevilla, JMF ;
Fernández, FGA ;
Grima, EM ;
Chisti, Y .
ENZYME AND MICROBIAL TECHNOLOGY, 2003, 33 (2-3) :270-277
[15]   THE PRODUCTION OF ORGANIC-ACIDS [J].
MATTEY, M .
CRITICAL REVIEWS IN BIOTECHNOLOGY, 1992, 12 (1-2) :87-132
[16]  
MICHAEL DG, 1985, J BACTERIOL, V162, P704
[17]   Fungal morphology and metabolite production in submerged mycelial processes [J].
Papagianni, M .
BIOTECHNOLOGY ADVANCES, 2004, 22 (03) :189-259
[18]  
PARK C, 2004, Patent No. 2004033570
[19]   Lovastatin production by Aspergillus terreus in a two-staged feeding operation [J].
Porcel, Elisa M. Rodriguez ;
Lopez, Jose L. Casas ;
Perez, Jose A. Sanchez ;
Chisti, Yusuf .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2008, 83 (09) :1236-1243
[20]  
SORENSEN J, 2003, THESIS U ALBERTA EDM