Wine Chemistry and Biochemistry

(Steven Felgate) #1

662 M. Dubernet


Characteristics of the Method


Intra-laboratory reproducibility: 0.4g/L
Inter-laboratory reproducibility: 0.6g/L

12.3.4.6 Determination ofL-Lactic Acid in Wines and Musts


Principle


Enzymatic Method


L-Lactic acid, in the presence of NAD, is oxidised to pyruvate in a reaction catal-


ysedL-lactate deshydrogenase (L-LDH). The equilibrium of the reaction is forced


in the direction of the products by the elimination of pyruvate by reacting it with


L-glutamate, resulting in the formation ofL-alanine. This reaction is catalysed by


glutamate-pyruvate-transaminase (GPT):


L-lactate+NAD+−>pyruvate+NADH+H+
( in the presence ofL-lactate deshydrogenase)

Pyruvate+L-glutamate−> L-alanine+α−cetoglutarate
( in the presence of GPT)

The formation of NADH, measured by the increase in its absorbance at 340 nm,


is proportional to the quantity of lactate initially present.


Characteristics of the Method


Intra-laboratory reproducibility: 0.2g/L
Inter-laboratory reproducibility: 0.5g/L

12.3.4.7 Determination of Total Phenolic Compounds in by the Folin-Ciocalteu


Index


Principle


Chemical Method


Total wine polyphenols are oxidised by the Folin-Ciocalteu reagent – composed of


a mixture of phosphotungstic and phosphomolybdic acids which are reduced by the


oxidation of the phenols, forming a mixture of blue oxides of tungsten and molyb-


denum. The blue coloration has an absorption maximum at approximately 750 nm,


the intensity of which is proportional to the level of phenolic compounds present


in the wine. The sequential analyser method is a direct automation of the manual


method and results are expressed as a unit-less index.

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