Towards a high-yield bioconversion of ferulic acid to vanillin

被引:194
作者
Muheim, A [1 ]
Lerch, K [1 ]
机构
[1] Givaudan Roure Res Ltd, CH-8600 Dubendorf, Switzerland
关键词
D O I
10.1007/s002530051416
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
Natural vanillin is of high interest in the flavor market. Microbial routes to vanillin have so far not been economical as the medium concentrations achieved have been well below 1 g l(-1). We have now screened microbial isolates from nature and known strains for their ability to convert eugenol or ferulic acid into vanillin. Ferulic acid, in contrast to the rather toxic eugenol, was found to be an excellent precursor for the conversion to vanillin, as doses of several g l(-1) could be fed. One of the isolated microbes, later identified as Pseudomonas putida, very efficiently converted ferulic acid to vanillic acid. As vanillin was oxidized faster than ferulic acid, accumulation of vanillin as an intermediate was not observed. A completely different metabolic flux was observed with Streptomyces setonii. During the metabolism of ferulic acid, this strain accumulated vanillic acid only to a level of around 200 mg l(-1) and then started to accumulate vanillin as the principal metabolic overflow product. In shake-flask experiments, vanillin concentrations of up to 6.4 g l(-1) were achieved with a molar yield of 68%. This high level now forms the basis for an economical microbial production of vanillin that can be used for flavoring purposes.
引用
收藏
页码:456 / 461
页数:6
相关论文
共 29 条
[11]   Kinetics of vanillin production from om Kraft lignin oxidation [J].
Fargues, C ;
Mathias, A ;
Rodrigues, A .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (01) :28-36
[12]   Metabolism of ferulic acid to vanillin - A bacterial gene of the enoyl-SCoA hydratase/isomerase superfamily encodes an enzyme for the hydration and cleavage of a hydroxycinnamic acid SCoA thioester [J].
Gasson, MJ ;
Kitamura, Y ;
McLauchlan, WR ;
Narbad, A ;
Parr, AJ ;
Lindsay, E ;
Parsons, H ;
Payne, J ;
Rhodes, MJC ;
Walton, NJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (07) :4163-4170
[13]  
Hausler A, 1997, ASM NEWS, V63, P551
[14]  
HERRMANN K, 1976, FORTSCHR CHEM ORG NA, V35, P73
[15]   Conversion of ferulic acid into 4-vinylguaiacol, vanillin and vanillic acid in model solutions of shochu [J].
Koseki, T ;
Ito, Y ;
Furuse, S ;
Ito, K ;
Iwano, K .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1996, 82 (01) :46-50
[16]   Biotechnological production of flavours and fragrances [J].
Krings, U ;
Berger, RG .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1998, 49 (01) :1-8
[17]  
Labuda I.M., 1994, US Patent, Patent No. [5,279,950, 5279950]
[18]   ALDEHYDE DEHYDROGENASES AND THEIR ROLE IN CARCINOGENESIS [J].
LINDAHL, R .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 27 (4-5) :283-335
[19]  
Markus P. H., 1992, EP, Patent No. [0542348, 542348]
[20]  
MUHEIM A, 1998, Patent No. 97110010