Kinetic analysis and modeling of the liquid-liquid conversion of emulsified di-rhamnolipids by Naringinase from Penicillium decumbens

Biotechnology and Bioengineering

Volumn 102, Issue 1, 2009, Pages 9-19

  Magario, I ^a   Vielhauer, O ^a,b   Neumann, A ^a   Hausmann, R ^a   Syldatk, C ^a  

^a UNIVERSITY OF KARLSRUHE   (Germany)

^b UNIVERSITY OF STUTTGART   (Germany)

Author keywords

Liquid liquid biocatalysis; Micellar substrates; Naringinase; Rhamnolipids

Indexed keywords

AQUEOUS PHASE; ENZYMATIC CONVERSIONS; ENZYMATIC REACTIONS; EXPERIMENTAL DATUM; KINETIC ANALYSIS; L RHAMNOSE; LIQUID-LIQUID BIOCATALYSIS; LIQUID-PHASE; MICELLAR SUBSTRATES; MICHAELIS-MENTEN KINETICS; NARINGINASE; PENICILLIUM DECUMBENS; RHAMNOLIPID; RHAMNOLIPIDS; TIME COURSE;

AGGREGATES; EMULSIFICATION; REACTION KINETICS; SUBSTRATES; SURFACE ACTIVE AGENTS;

REACTION RATES;

FUNGAL ENZYME; NARINGINASE; RHAMNOLIPID; RHAMNOSE; UNCLASSIFIED DRUG; BETA GLUCOSIDASE; FUNGAL PROTEIN; GLYCOLIPID; MULTIENZYME COMPLEX; SURFACTANT;

ARTICLE; BIOTRANSFORMATION; ENZYME ACTIVITY; ENZYME KINETICS; ENZYME MECHANISM; EXPERIMENTAL MODEL; MICHAELIS MENTEN KINETICS; PENICILLIUM; PENICILLIUM DECUMBENS; PH; PHASE TRANSITION; TEMPERATURE; EMULSION; ENZYMOLOGY; KINETICS; METABOLISM; THEORETICAL MODEL;

PENICILLIUM DECUMBENS;

BETA-GLUCOSIDASE; EMULSIONS; FUNGAL PROTEINS; GLYCOLIPIDS; HYDROGEN-ION CONCENTRATION; KINETICS; MODELS, THEORETICAL; MULTIENZYME COMPLEXES; PENICILLIUM; RHAMNOSE; SURFACE-ACTIVE AGENTS; TEMPERATURE;

EID: 58149218800     PISSN: 00063592     EISSN: 10970290     Source Type: Journal    
DOI: 10.1002/bit.22057     Document Type: Article

References (30)

1. Attwood D, Florence AT. 1983. Surfactant systems: Their chemistry, pharmacy and biology. London: Chapman and Hall.
2. Banat IM, Makkar RS, Cameotra SS. 2000. Potential commercial applications of microbial surfactants. Appl Microbiol Biotechnol 53(5):495- 508.
3. Champion JT, Gilkey JC, Lamparski H, Retterer J, Miller RM. 1995. Electron-microscopy of rhamnolipid (biosurfactant) morphology Effects of pH, cadmium, and octadecane. J Colloid Interf Sci 170(2): 569-574.
4. Chopineau J, Lesieur S, Carion-Taravella B, Ollivon M. 1998. Self-evolving microstructured systems upon enzymatic catalysis. Biochimie 80(5- 6):421-435.
5. Deems RA, Eaton BR, Dennis EA. 1975. Kinetic-analysis of phospholipase- a2 activity toward mixed micelles and its implications for study of lipolytic enzymes. J Biol Chem 250(23):9013-9020.
6. Giani C, Wullbrandt D, Reinhardt R, Meiwes J, Hoechst AG, assignee. 1993. Pseudomonas aeruginosa and its use in a process for the biotechnological preparation of L-rhamnose. Germany patent US5501966.
7. Holland PM, Rubingh DN. 1992. Mixed surfactant systems-An overview. ACS Symp Ser 501:2-30.
8. Ishigami Y, Gama Y, Nagahora H, Yamaguchi M, Nakahara H, Kamata T. 1987. The pH-sensitive conversion of molecular aggregates of rhamo lipid bisurfactant. Chem Lett (5):763-766.
9. Lang S, Trowitzsch-Kienast W. 2002. Biotenside. Stuttgart Leipzig Wiesbaden: Teubner.
10. Lebron-Paler A, Pemberton JE, Becker BA, Otto WH, Larive CK, Maier RM. 2006. Determination of the acid dissociation constant of the biosurfactant monorhamnolipid in aqueous solution by potentiometric and spectroscopic methods. Anal Chem 78(22):7649-7658.
11. Levenspiel O. 1999. Chemical reaction engineering. John Wiley & Sons.
12. Linhardt RJ, Bakhit R, Daniels L, Mayerl F, Pickenhagen W. 1989. Microbially produced rhamnolipid as a source of rhamnose. Biotechnol Bioeng 33(3):365-368.
13. Magario I, Neumann A, Oliveros E, Syldatk C. 2008a. Deactivation kinetics and response surface analysis of the stability of alpha-l-rhamnosidase from Penicillium decumbens. Appl Biochem Biotechnol (in press). DOI: 10.1007/s12010-008-8204-5.
14. Magario I, Xiaotian M, Neumann A, Syldatk C, Hausmann R. 2008b. Non- porous magnetic micro-particles: Comparison to porous enzyme carriers for a diffusion rate-controlled enzymatic conversion. J Biotechnol 134:72-78. 10.1016/j.jbiotec.2007.12.001.
15. Meiwes J, Wullbrandt D, Giani C, Hoechst AG, assignee. 1997. alpha -l- rhamnosidase for obtaining rhamnose, a process for its preparation and its use. Germany patent US5641659.
16. Michon F, Pozsgay V, Brisson JR, Jennings H J. 1989. Substrate- specificity of naringinase, an alpha-L-rhamnosidase from Penicillium decumbens. Carbohydr Res 194:321-324.
17. Milioto S. 2006. Mixed micellar systems. In: Somasundaran P, editor. Encyclopedia of surface and colloid science. 2nd edn. New York: Taylor & Francis. p 3233-4198.
18. Mixich J, Rapp K, Vogel M, Suedzucker AG, assignee. 1996. Method for the preparation of rhamnose monohydrate from rhamnolipids. Germany patent US5550227.
19. Mulligan CN. 2005. Environmental applications for biosurfactants. Environ Pollut 133(2):183-198.
20. Nitschke M, Costa S, Contiero J. 2005. Rhamnolipid surfactants: An update on the general aspects of these remarkable biomolecules. Biotechnol Prog 21(6):1593-1600.
21. Ozdemir G, Peker S, Helvaci SS. 2004. Effect of pH on the surface and interfacial behavior ofrhamnolipids R1 and R2. Colloids SurfA 234(1-3):135-143.
22. Panaiotov I, Ivanova M, Verger R. 1997. Interfacial and temporal organization of enzymatic lipolysis. Curr Opin Colloid Interf Sci 2(5):517-525.
23. Redondo O, Herrero A, Bello JF, Roig MG, Calvo MV, Plou FJ, Burguillo FJ. 1995. Comparative kinetic-study of lipase-A and lipase-B from Candida rugosa in the hydrolysis of lipid P-nitrophenyl esters in mixed micelles with Triton-X-100. Biochim Biophys Acta 1243(1):15-24.
24. Romero C, Manjon A, Bastida J, Iborra JL. 1985. A method for assaying the rhamnosidase activity of naringinase. Anal Biochem 149(2):566- 571.
25. Rubingh DN. 1996. The influence of surfactants on enzyme activity. Curr Opin Colloid Interf Sci 1(5):598-603.
26. Rubingh DN, Bauer M. 1992. Lipase catalysis of reactions in mixed micelles. ACS Symp Ser 501:210-226.
27. Schenk T, Schuphan I, Schmidt B. 1995. High-performance liquid-chromatographic determination of the rhamnolipids produced by Pseudomonas aeruginosa. J Chromatogr A 693(1):7-13.
28. Straathof AJJ. 2003. Enzymatic catalysis via liquid-liquid interfaces. Bio-technol Bioeng 83(4):371-375.
29. Syldatk C, Lang S, Wagner F, Wray V, Witte L. 1985. Chemical and physical characterization of four interfacial-active rhamnolipids from Pseudomonas spec. DSM 2874 grown on n-alkanes. Z Naturforsch [C] 40(1- 2):51-60.
30. Trummler K, Effenberger F, Syldatk C. 2003. An integrated microbial/enzymatic process for production of rhamnolipids and L-(+)-rham- nose from rapeseed oil with Pseudomonas sp DSM 2874. Eur J Lipid Sci Technol 105(10):563-571.