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STRATEGIES FOR THE DEVELOPMENT OF MALATE SENSORS DEVOTED TO WINEMAKING MONITORING
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WHY TO DETECT MALIC ACID ? THE MALOLACTIC FERMENTATION (MLF) MLF = secondary fermentation, occurs after alcoholic fermentation, lasts from 2 weeks to several months (if T is too low). -Transformation of malic acid (diacide) in lactic acid (monoacide) - Bacterial process (Oenococcus oeni) - Deacidification: decrease in titratable acidity and increase in pH - Wine stabilisation and flavour change MLF is usually encouraged for all dry red wines: [Malic acid] in musts: 1-5 g/L [Malic acid] in red wines : 0-0.1 g/L MLF is avoided or partially performed for white wines. MONITORING OF MLF IS FUNDAMENTAL FOR WINE PRODUCERS.
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SUBSTRATES OF INTEREST CO 2 COOH CHOH CH 3 L-malate L-lactate MALOLACTIC FERMENTATION (Oenococcus oeni) COOH CHOH CH 2 COOH ALCOHOLIC FERMENTATION ( Saccharomyces cerevisiae) O COOH C CH 3 CO 2 H C CH 3 O NADH + H + NAD + CH 2 OH CH 3 Pyruvate decarboxylase Alcool dehydrogenase Sugars Ethanal Ethanol Pyruvate Acetobacter Acetic acid Lactic bacteria D-lactate
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Legend : T - Tartaric acid L - Lactic acid M - Malic acid WIDELY USED METHOD : PAPER CHROMATOGRAPHY Suitable for any winery Low cost but low speed and accuracy.
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ENZYMATIC RECOMMENDED METHOD L-malate Oxaloacetate + NAD + + NADH + H + Spectrophotometric determination at 340nm ( = 6300 M -1.cm -1 ) GOT* + L-glutamate L-aspartate + 2-oxoglutarate * Glutamate-oxaloacetate transaminase (EC2.6.1.1) Costly, not adapted to small wineries Laboratory analysis : delays between sampling and results. Malate dehydrogenase L-MDH (EC 1.1.1.37) Need of easy and portable analytical devices as BIOSENSORS
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+ NAD + PRINCIPLE OF DH-BASED BIOSENSORS DEHYDROGENASE (DH) SUBSTRATE PRODUCT + NADH + H + Optical detection ( =340 nm ) AMPEROMETRIC DETECTION Direct oxidation High Potential No selectivity Bienzymatic systems Mediated oxidation (monoenzymatic system)
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+ NAD + THE MALATE DEHYDROGENASE-REACTION : DIFFERENT OPTIONS FOR SENSOR DEVELOPMENT Malate dehydrogenase L-MDH (EC 1.1.1.37) L-malate Oxaloacetate + NADH + H + High concentrations of NAD + + appropriate mediator Enzymatic consumption of NADH (regeneration of NAD + ) MONO-ENZYMATIC SENSOR BI-ENZYMATIC SENSOR
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Diaphorase (Clostridium kluyverii) 2 Fe(CN) 6 3- 250 mV vs. SCE 2 e- 2 Fe(CN) 6 4- NADH + H + NAD + BI-ENZYMATIC SYSTEM BASED ON DIAPHORASE ( EC 1.8.1.4) Mandatory addition of ferricyanide Interferences with wine samples * Related papers : 1. J.-L. Marty and T. Noguer. Analusis, 21 (1993) 6-8. 2. T. Noguer and J.-L. Marty. Enzyme Microb. Technol., 17 (1995) 453-456. 3. T. Noguer and J.-L. Marty. Anal. Chim. Acta, 347 (1997) 63-70.
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NADH oxidase ( Thermus thermophilus) O2O2 650 mV vs. Ag/AgCl H 2 O 2 NADH + H + NAD + 2 e- Dissolved in solution High stability BI-ENZYMATIC SYSTEM BASED ON NADH OXIDASE ( EC 1.6.99) High overpotential for H 2 O 2 oxidation : high interferences * Related papers : 1. T. Noguer and J.-L. Marty. Anal. Let., 30 (1997) 1069-1080. 2. T. Noguer, A. Gradinaru, A. Ciucu and J.-L. Marty. Anal. Let., 32 (9) (1999) 1723-1738.
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Fe 4 [Fe(CN) 6 ] 3 Prussian Blue Fe 4 K 4 [Fe(CN) 6 ] 3 Prussian White 2NADOX (FMNH 2 ) 2 NADH + 2 H + 2 NAD + Mediator Working electrode Sensing layer 4 e - Solution -150 mV vs Ag/AgCl 2NADOX (FMN) 4 K + 4 H + + 4K + BI-ENZYMATIC SYSTEM INVOLVING PRUSSIAN BLUE AS MEDIATOR 1/2 O 2 + H 2 O Fe 4 [Fe(CN) 6 ] 3 Prussian Blue Fe 4 K 4 [Fe(CN) 6 ] 3 Prussian White 2NADOX (FMNH 2 ) 2 NADH + 2 H + 2 NAD + 2H 2 O 2 4 OH - + 4K + Mediator 4 e - Solution 2NADOX (FMN) 4 K + Working electrode Sensing layer -150 mV vs Ag/AgCl Precipitated on WE surface NAD and FMN must be added in solution
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NADH NAD + MB + MBH H + + 2e - Malic acid Oxaloacetic acid - 150 mV vs Ag/AgCl L-MDH MONO-ENZYMATIC SYSTEM INVOLVING MELDOLA’S BLUE AS MEDIATOR In solution Incorporated in the electrode material MB : FAST EXCHANGE OF ELECTRONS WITH NADH
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10% MBRS-modified SPE, pyrophosphate buffer 0.1 M, pH 9.3 Gallic acid 1 mM, 50 µL red wine (Caramany) WORKING AT -150 MV VS Ag/AgCl ALLOWS REDUCING INTERFERENCES MELDOLA’S BLUE-MODIFIED ELECTRODES : EVALUATION OF INTERFERENCES DUE TO WINE PHENOLIC COMPOUNDS
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(Batch measurements in stirred buffered solution) PB AND MB-BASED SENSORS : COMPARATIVE TABLE
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REAL SAMPLES ANALYSIS COMPARISON WITH COMMERCIALLY AVAILABLE KITS GOOD CORRELATIONS BUT NAD (and FMN) MUST BE ADDED IN REACTIONAL MEDIUM RESEARCHS FOCUS ON OBTENTION OF A FAD-BOUND NADH OXIDASE (GTP Technology, Labège, France)
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MQO from Corynebacterium glutamicum is a FAD-dependent peripheral membrane enzyme (FAD tightly bound). Involved in citric acid cycle.- Natural aceptor : ubiquinone (ménaquinone) AN ALTERNATIVE TO THE CLASSICAL MDH : THE MALATE:QUINONE OXIDOREDUCTASE ( MQO,EC 1.1.99.16). Alternative metabolic pathway (PEP shunt) for the conversion of malate to oxaloacetate in E. coli. Van der Rest et al., J Bacteriol. 182(24) (2000) 6892-6899
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MQO-FAD MQO-FADH 2 Med ox Med red e-e- L-Malic acidOxaloacetic acid MQO used in this work in a recombinant enzyme (E. coli) produced by GTP Technology, Labège (France). NO COENZYME NEEDED, MONOENZYMATIC SYSTEM REACTION ESSENTIALLY IRREVERSIBLE BUT : APPROPRIATE MEDIATORS MUST BE FOUND THE PRINCIPLE OF MQO-BASED BIOSENSOR
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SELECTION OF MEDIATOR(S) FOR MQO Analytical responses of the sensors to 1 mM malic acid (0,134g/L) (Working potentials were selected by cyclic voltammetry) High Interferences
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MQO-BASED SENSORS PERFORMANCES
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Evaluation of interferences HIGH INTERFERENCES USING DPIP AS MEDIATOR AS : Analytical signal (to 1mM malate), IS = Interference signal (to 100-fold diluted red wine or 0.05 mM gallic acid)
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REAL SAMPLES ANALYSIS Wine analysis using MQO biosensors using DPIP or PMS as mediators. Average of triplicate measurements, spiked wine samples.
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MQO : cofactorless enzyme, irreversible conversion of malate BUT :Poor stability, supplied in (NH 4 ) 2 SO 4 by GTP technology, must be desalted before immobilization : loss of activity Mediators : DPIP and PMS were used in solution, high interferences with DPIP,low stability of PMS (light sensitive). Appropriated mediators still must be found : * Efficient electronic transfert with FADH 2, * Low detection potential, reduced interactions with polyphenolic compounds * Incorporable in screen-printed electrodes Advantages & Drawbacks of MQO-sensor
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