METHOD FOR THE OPTIMISATION OF ORGANOLEPTIC PROPERTIES IN VEGETABLE PRODUCTS CONTAINING CHLOROPHYLLOUS PIGMENTS

Abstract

The object of the present invention is a method that enables organoleptic properties, in particular colour, to be optimised in fruits and vegetables containing chlorophyll pigments. For this purpose, the method is based on known techniques, such as treatment with compounds containing Zn, improving the obtained results by means of a treatment with a buffered acid solution.

In this way, products can be produced having a permanent bright green colour, without exceeding the quantity of Zn that is legally permitted, while leaving other organoleptic characteristics, such as flavour, unaltered. The method can be applied, in particular, to green table olives, and preferably to green tables olives processed by means of alkaline treatment and without fermentation.

Claims

1. A method for optimising organoleptic properties in vegetable products containing chlorophyll pigments which comprises: treating of the vegetable products with at least one zinc compound; treating of the vegetable products from the previous step with a buffered base solution; and heat treating for preservation, and characterised in that the vegetable products are subjected to a treatment with a buffered acid solution that takes place before the treatment with the buffered base solution.

2. The method according to claim 1, characterised in that the organoleptic property to be optimised is the green colour.

3. The method according to claim 1, characterised in that the zinc compound is a zinc salt selected from among zinc acetate, zinc bisglycinate, zinc chloride, zinc citrate, zinc gluconate, zinc lactate, zinc oxide, zinc carbonate, zinc sulphate or combinations thereof.

4. The method according to claim 3, characterised in that the treatment with the zinc salt consists of putting the vegetable products in contact with a solution of the zinc salt having a concentration comprised between 0.005 and 3 g/L, in a solid/liquid ratio equal to or greater than 1:1 (w/v), for a period of time comprised between 5 minutes and 1 year, and at a temperature between 15? C. and 129? C.

5. The method according to claim 1, characterised in that the buffered base solution is selected from among a buffered solution of borate, tris(hydroxymethyl)aminomethane, glycine, phosphate or carbonate or combinations thereof.

6. The method according to claim 5, characterised in that the treatment with the buffered base solution consists of putting the vegetable products in contact with the solution having a concentration equal to or greater than 0.1M, in a solid/liquid ratio equal to or greater than 1:1 (w/v), for a period of time comprised between 5 minutes and 1 year, and at a temperature between 15? C. and 129? C.

7. The method according to claim 1, characterised in that the buffered acid solution is selected from among acetic acid, ascorbic acid, benzoic acid, citric acid, lactic acid, malic acid, propionic acid, succinic acid or combinations thereof.

8. The method according to claim 7, characterised in that the treatment with the buffered acid solution consists of putting the vegetable products in contact with the solution having a concentration equal to or greater than 0.1M, in a solid/liquid ratio equal to or greater than 1:1 (w/v), for a period of time comprised between 1 minute and 10 days, and at a temperature between 15? C. and 90? C.

9. The method according to claim 7, characterised in that the treatment with the buffered acid solution takes place before the treatment with the zinc salt.

10. The method to claim 7, characterised in that the treatment with the buffered acid solution takes place at the same time as the treatment with the zinc salt.

11. The method according to claim 1, characterised in that the treatment with the buffered base solution takes place at the same time as the treatment with the zinc salt.

12. The method according to claim 11, characterised in that the treatment with the buffered base solution takes place at the same time as the treatment with the zinc salt and at the same time as a heat treatment for sterilisation.

13. The method according to claim 1, characterised in that it further includes at least one of the following steps: washing of the vegetable products packing in brine

14. The method according to claim 1, characterised in that the vegetable products are green table olives.

15. The method according to claim 14, characterised in that the vegetable products are green table olives processed by means of alkaline treatment and without fermentation.

16. The method according to claim 15, characterised in that the green table olives processed by means of alkaline treatment and without fermentation are subjected to: treating with buffered lactic acid/NaOH acid solution at a concentration equal to or greater than 0.1M and pH equal to or less than 5, and in a solid/liquid ratio equal to or greater than 1:1, and containing NaCl in a proportion between 3 and 6%, for a period of time between 1 minute and 10 days, and at a temperature between 15? C. and 90? C.; treating with zinc acetate for a period of time comprised between 5 minutes and 1 year, and at a temperature between 15? C. and 129? C., in a concentration between 0.05 g/L and 0.5 g/L, and in a solid/liquid ratio equal to or greater than 1:1 (w/v); treating with buffered glycine/NaOH base solution, in a concentration equal to or greater than 0.1M and pH between 8 and 10, in a solid/liquid ratio equal to or greater than 1:1 (w/v) and for a period of time comprised between 5 minutes and 1 year, and at a temperature between 15? C. and 129? C.; washing of the green olives with water for a period of time between 3 and 24 h, and with a number of washes between 0 and 5, based on the concentration of zinc used in an earlier treatment; packing in NaCl brine in a concentration between 3 and 6%; heat treating that is selected from among sterilisation for 15 F.sub.0, at a temperature between 117? C. and 129? C. and a time between 5 and 43 minutes, or pasteurisation at 80? C., for a time between 6 and 14 minutes.

17. The method according to claim 16, characterised in that: the treating with the buffered lactic acid/NaOH acid solution takes place at a pH equal to 4 in a solid/liquid ratio of 1:3 (w/v), containing NaCl at 4% (w/v) for 9 days and at a temperature of 30? C. the treating with zinc acetate is carried out at a concentration of 0.1 g/L and simultaneous to the treatment with the buffered base solution, which takes place at a pH equal to 9.5, includes NaCl at 4% and maintains a period of equilibrium of 48 h at a temperature of 30? C., followed by 43 minutes of sterilisation at 117? C.

18. Green table olives processed by means of alkaline treatment and without fermentation and prepared by means of a method as defined in claim 16, characterised in that they simultaneously have a percentage of Zn-chlorophyll complexes comprised between 15% and 75% and less than 0.0075% of Zn.

Description

DESCRIPTION OF THE FIGURES

[0048] FIG. 1: Effect of the treatment with zinc acetate at pH 5 on the green colour of the table olive, estimated based on the parameter a*. The Zn.sup.2+ ions are added in a concentration of 3 g/L (3000 ppm) in a 0.1 M acetic acid/acetate buffer solution, at pH 5 and containing 6% of NaCl (w/v). ? with Zn.sup.2+ ? control without Zn.sup.2+. Note: Accelerated storage test, consisting of subjecting the treated olives at a temperature of 55? C. for 24 hours.

[0049] FIG. 2: Typical reversed-phase HPLC chromatograms with detection at 640 nm, for separating chlorophylls, Mg-free chlorophyll derivatives and zinc metal-chlorophyll complexes in olives of the Manzanilla variety, according to the different phases of the Castelvetrano-style production process (CSP) and embodiment of the invention according to example no. 1: (A) Fresh fruit; (B) CSP fruit; (C) CSP fruit subsequently treated with 3 g/L (3000 ppm) of Zn.sup.+2 ions dissolved in NaCl brine at 4% (w/v), buffered at pH 5 with 0.1 M of acetic acid/acetate: (C.sub.1) for 14 days, (C.sub.2) for 6 months, (C.sub.3) for 10 days+accelerated storage test (24 h at 55? C.). Identification of peaks: Chlorophylls: 3. Chlorophyll b; 4. Chlorophyll a; Precursors of the zinc metal-chlorophyll complexes of the series a: 1. 15.sup.2 methyl-phytol-chlorin e.sub.6 ester; 9. Pheophytin a; 10. Pheophytin a; 11. Pyropheophytin a. Zinc metal-chlorophyll complexes of the series a: 2. Zn-15.sup.2 methyl-phytol-chlorin e.sub.6 ester; 5. Zn-15.sup.1-OH-Lactone Pheophytin a; 6. Zn-Pheophytin a; 7. Zn-Pheophytin a; 8. Zn-Pyropheophytin a.

[0050] FIG. 3: Typical reversed-phase HPLC chromatograms with detection at 640 nm, for separating chlorophylls, Mg-free chlorophyll derivatives and zinc metal-chlorophyll complexes in olives of the Manzanilla variety, according to the different phases of the Castelvetrano-style production process (CSP) and embodiment of the invention according to example no. 4: (A) Fresh fruit; (B) CSP fruit; (C) CSP fruit after 9 days of acid treatment in NaCl brine at 4% (w/v), buffered at pH 4 with 0.1 M of lactic acid/NaOH (CSP+Ac); (D) CSP+Ac and sterilised at 117? C. for 43 minutes, in a solution at 4% of NaCl (w/v) and 0.1 M of glycine/NaOH at pH 9.5, containing 0.1 g/L (100 ppm) of Zn.sup.+2 ions.

DETAILED DESCRIPTION OF THE INVENTION

[0051] The present invention relates to methods for improving the green colour of canned fruits or vegetables, in particular table olives, using a food grade salt zinc, without the amount of Zn (II) incorporated into the product exceeding the legally established limits (0.075 g/kg; 75 ppm). Although the method can be applied to any product that contains chlorophyll pigments (chlorophylls and/or chlorophyll derivatives), the product is, in particular, the green table olive processed by means of alkaline treatment and without fermentation, and the food additive is zinc acetate (E-650).

[0052] The invention encompasses any production phase of the table olive when zinc salts are used therein to improve the colour, and it aims to improve the colour of the product by forming zinc metal-chlorophyll complexes (Zn-Cls) with a bright green colour and high stability. The method can comprise the following steps:

A) treatment with a buffered acid solution
B) treatment with at least one zinc salt
C) treatment with a buffered base solution
D) washes
E) packing in brine
F) heat treatment for preservation

[0053] The re-greening of the product is attributed to the formation of zinc metal-chlorophyll complexes, mainly Zn-pheophytin a, Zn-pyropheophytin a and Zn-15.sup.2-Methyl-phytol-chlorin e.sub.6 ester.

[0054] In the present invention, the term chlorophyll pigment refers to a coloured compound with a chemical structure derived from chlorophyll, in other words, formed by a porphyrin ring substituted with an additional isocyclic ring, which can be open, and a propionic acid moiety esterified or not with a terpene chain called phytol. The porphyrin ring is a tetrapyrrole, with four pyrrole rings linked to form a larger ring that is the porphyrin. In the case of chlorophyll, a Mg.sup.2+ atom, bonded to the nitrogens of the pyrrole groups, is located in the centre of the porphyrin, but this Mg.sup.+2 atom can be substituted by Zn.sup.2+, Cu.sup.2+ or 2H.sup.+ to form other chemically stable pigments.

[0055] The term green table olive refers to a product that is prepared using healthy fruits of cultivated olive varieties, harvested during the ripening period, prior to colouring, when they have reached their normal size, and they are subjected to treatments to eliminate the natural bitterness preserved by means of natural fermentation or heat treatment, with or without preservatives, and packed with covering liquid. Examples of green table olives are green olives treated in brine, untreated green olives, or olive specialties processed by means of alkaline treatment and without fermentation, which have characteristics and specific names in the different producer countries: Campo Real in Spain, Castelvetrano in Italy, Picholine in France, and California-style green olives or green ripe olives in the United States.

[0056] In the present invention, the term treatment with a buffered acid solution (step A) refers to the immersion of the vegetable material in a buffer solution at acid pH for a certain period of time. According to a preferred embodiment, the buffer is lactic acid/NaOH at a concentration of 0.1 M and pH ?5, preferably 4, containing NaCl in a proportion between 3 and 6%, preferably 4% (w/v), and in a solid/liquid ratio equal to or greater than 1:1 and preferably 1:3 (w/v). The treatment time is between 1 minute and 30 days, preferably 9 days, at a temperature between 15? C. and 90? C., preferably a controlled temperature of 30? C.

[0057] In the present invention, the term treatment with a zinc salt (step B) refers to the immersion of the vegetable material for a period of time in a buffer solution containing NaCl and a zinc salt. The zinc salt is a food grade water-soluble salt, preferably the zinc acetate food additive (E-650), and in a concentration between 0.005 g/L (5 ppm) and 3 g/L (3000 ppm), preferably 100 ppm and in a solid/liquid ratio equal to or greater than 1:1 (w/v). The treatment time is between 1 minute and 1 year, preferably 72 h and the temperature is between 15? C. and 129? C.

[0058] In the present invention, the term treatment with a buffered base solution (step C) refers to the immersion of the vegetable material for a period of time in a buffer solution at alkaline pH for a certain period of time. According to a preferred embodiment, the buffer is glycine/NaOH, in a concentration ?0.1 M and pH between 8 and 10, preferably 9.5. The proportion of NaCl can be between 3 and 6%, preferably 4% (w/v) and in a solid/liquid ratio ?1:1 and preferably 1:1 (w/v). The treatment time is between 5 minutes and 1 year, preferably 72 h, at a temperature between 15? C. and 129? C.

[0059] The addition of the zinc salt (step B) can be carried out in the buffered acid solution (step A) or in the buffered base solution (step C) irrespectively.

[0060] In the present invention, the term washes (step D) refers to successive treatments of the vegetable material with water for a period of time. In a preferred embodiment, the treatment is carried out through immersion of the fruit in water for a period of time between 3 and 24 h, preferably 12 h and the number of washes is between 0 and 5, based on the concentration of zinc used in an earlier step.

[0061] In the present invention, the term packing in treating brine (step E) refers to the immersion of the vegetable material in NaCl brine in a concentration between 3 and 6%, preferably 4% (w/v). If the concentration of the zinc acetate additive in step B is ?0.1 g/L (100 ppm), the steps of washes (step D) and packing in treating brine (step D) are eliminated from the method.

[0062] In the present invention, the term heat treatment for preservation refers to a heat treatment that ensures the long-term safety of the product. In a preferred embodiment, the heat treatment is sterilisation for 15 F.sub.0, at a temperature between 117? C. and 129? C., preferably at 117? C. for a period of time of 43 minutes. In another preferred embodiment, the treatment is pasteurisation at 80? C., for a time between 6 and 14 minutes, preferably 6 min.

[0063] To analyse chlorophyll pigments, a specific extraction technique that has been developed by M?nguez-Mosquera and Garrido-Fern?ndez (Chlorophyll and carotenoid presence in olive fruit, Olea europaea. J. Agric. Food Chem. (1989) 37, 1-7) is required. The technique is based on the selective distribution of components between N,N-Dimethylformamide (DMF) and hexane. In the hexane phase, the lipids, the fraction of carotenes and diesterified xanthophylls remain, while the DMF phase retains the chlorophyll compounds and free and monoesterified xanthophylls. This system provides a solution for pigments that is free of the fatty material that is characteristic of these fruits and that interferes in the subsequent separation and identification of the pigments.

[0064] Once the purified extract of pigments is obtained, the separation and quantification of pigments is carried out by means of HPLC with a reversed-phase column (20?0.46 cm) packed with Mediterranea-Sea C18 (3 ?m) (Teknokroma, Barcelona, Spain). The column is protected with a precolumn (1?0.4 cm) packed with the same material. The separation is carried out at a flow rate of 1.25 mL/min, by means of a gradient elution system that uses two solvent mixtures: A.Water/ion suppression reagent/methanol (1:1:8 v/v/v) and B.methanol/acetone (1:1 v/v). The ion suppression reagent is 0.05 M tetrabutylammonium acetate and 1 M ammonium acetate in water (M?nguez-Mosquera M I, Gandul-Rojas B, Monta?o-Asquerino A, Garrido-Fern?ndez J. Determination of chlorophylls and carotenoids by HPLC during olive lactic fermentation. J. Chromatogr. (1991) 585, 259-266). The gradient system used is an adaptation of the system described by Gandul-Rojas, Roca and Gallardo-Guerrero 2012 (Detection of the colour adulteration of green table olive with copper chlorophyllin complexes (E-141ii colorant). LWTFood Sci. Tech. (2012) 463, 11-318).

[0065] The spectrophotometric detection of the chlorophyll pigments is carried out at 666, 650, 640 and 626 nm and an online record of the UV-Vis absorption spectrum is obtained with a photodiode detector. The identification is made by co-chromatography with the corresponding standards and based on the spectral characteristics described in detail in specific publications (Gandul-Rojas et al. 2012). The quantification is carried out based on the corresponding calibration lines (amount vs integrated peak area). The calibration equations are obtained by means of least squares linear regression analysis in a concentration range according to the concentration levels of these pigments in table olives. Duplicate analyses of 5 different volumes of each standard solution are carried out.

[0066] To determine the content in zinc, 100 g of fruits that are washed, dried, pitted and chopped are used. Exactly 5 g of the resulting paste is weighed in a porcelain capsule and is placed in a muffle furnace. The temperature of the muffle is quickly brought to 100? C. and then it is slowly increased until it reaches the calcination temperature (550? C.), temperature at which it is maintained for 8-10 hours. The ashes, having a white-grey colour, are slightly moistened and they dissolve into three 2 mL portions of HCL 6 N, and it is slowly filtered through a paper filter into a 25 mL volumetric flask. Afterwards, the filter is cleaned three times with 3 mL of deionised water, which is also added to the volumetric flask, and it is finished by diluting to the mark with deionised water. The solution of the ashes is facilitated by slightly heating the capsule after each addition of HCl. At the same time, a blank test is prepared that only includes reagents (L?pez A, Garc?a P y Garrido A. Multivariate characterization of table olives according to their mineral nutrient composition. Food Chem. (2008) 106:369-378). Finally, the zinc content is determined with an atomic absorption spectrophotometer (GBC, model 932), spraying the sample on an air-acetylene flame and using a zinc hollow cathode lamp. The absorbency is measured at 213.9 nm with a slit of 0.5 nm (Hornero-M?ndez D, Gallardo-Guerrero L, J?ren-Gal?n M and M?nguez-Mosquera M I. Differences in the activity of superoxide dismutase, polyphenol oxidase and CuZn content in the fruits of Gordal and Manzanilla olive varieties. Z. Naturforsch. (2002) 57, 113-120). The colour measurement is obtained with a BYK-Gardner spectrophotometer, Model 9000, equipped with software for calculating the chromaticity coordinates on the CIE L* a* b* scale. The data for each measurement will be the average value obtained with 20 olives (Arroyo-L?pez F N, Romero C, Dur?n-Quintana M C, L?pez-L?pez A, Garc?a-Garc?a P and Garrido-Fern?ndez A. Kinetic study of the physicochemical and microbiological changes in seasoned olives during the shelf-life period. J. Agric. Food Chem. (2005) 53, 5285-5292). The changes in the green colour are expressed with the parameters L*, a*, b*, the ratio ?a*/b, hue (h) and chrome (C*) (Koca N, Karadeniz F, Burdurlu H S. Effect of pH on chlorophyll degradation and colour loss in blanched green peas. Food Chem. (2006) 100, 609-615).

Embodiment of the Invention

[0067] The invention is illustrated below by means of tests carried out by the inventors which reveal the effectiveness of the method described in the present invention.

[0068] Raw Material.

[0069] A 78 kg batch of olive fruits of the Manzanilla variety, mostly harvested in the yellowish-green state of maturity, was processed at laboratory scale as green table olives treated with alkali and without fermentation, according to the Castelvetrano style. Prior to the processing, a manual selection of the fruit was carried out, eliminating those that were damaged or in different states of maturity (olives changing colour from green to purple, purple olives and black olives). These selected fruits were deposited in 3.7 L PET containers and were covered with NaOH solution at 2% (w/v) (2.2 kg of fruit+1.8 L of alkaline solution). After one hour of treatment, 100 g of NaCl was added to each container (equivalent to a final concentration of 5.5% in the NaCl/NaOH solution) and the fruits were maintained in this alkaline brine for 15 days, after which three washes with water were carried out for 3.5 h, 18 h and 3.5 h. Finally, the fruits were placed in NaCl brine at 6% (w/v) and they were preserved in a cooled chamber at 4? C. until the use thereof.

Example No. 1: Pasteurised Product Prepared in Three Steps

[0070] a) Steps A and B: Treatment with Zinc Salt in a Buffered Acid Solution.

[0071] Treatment of green table olives prepared in the Castelvetrano style in a 0.1 M solution of the acetic acid/acetate buffer mixture at pH 5, containing 6% (w/v) of NaCl, and 3 g/L (3000 ppm) of Zn.sup.2+ ions as zinc acetate. The solid/liquid ratio is 1:3 and the treatment lasts 6 months at a room temperature of 25?3? C.

[0072] 445 mL glass jars (16 RefTO77) were filled with 20 olives (99-103 g) and 300 mL of the buffered brine containing 3 g/L (3000 ppm) of zinc acetate. The closed jars were kept in the laboratory at room temperature and in darkness, and they were analysed for colour and content in chlorophyll pigments at 2, 4, 7, 8, 9, 10 and 14 days. Finally, the fruits were stored for 6 months and alternatively, they were subjected to an accelerated storage test by means of heating in an oven at 55? C. for 24 h. At the same time, controls on packed fruits stored in identical conditions but without the addition of Zn.sup.2+ to the packing brine were carried out.

[0073] During storage, the loss of the green colour of the fruits, measured from the chromaticity coordinate a*, was very slow in the fruits packed with zinc, without this loss being significant in any case (p<0.05) (FIG. 1). However, the fruits not treated with zinc lost their green colour more quickly, which began to be significant as of day 9 (p<0.05). This loss of green colour was associated with the substitution reaction of Mg.sup.2+ for 2H.sup.+, which the chlorophylls and derivatives underwent under acid conditions. However, in the fruits treated with the Zn.sup.2+ salt, this reaction was offset by the insertion of this divalent metal in the porphyrin ring, causing the formation of metal-chlorophyll complexes of a stable green colour. On day 8, the formation of these zinc metal-chlorophyll complexes, the concentration of which slowly increased up to day 14, began to be detected in the series a (FIG. 2). The accelerated storage test led to very significant re-greening of the fruit treated with zinc, the value of a* even exceeding the initial value (?7.30).

[0074] This improvement in the colour was associated with the formation of different zinc metal-chlorophyll complexes, mostly in the series a (FIG. 2). Quantitively, the zinc metal-chlorophyll complexes are approximately 45% of the total chlorophyll pigments present in the olives subjected to the accelerated storage test (Table 1):

TABLE-US-00002 TABLE 1 Chromaticity coordinate a and content in chlorophyll pigments (%) and zinc (ppm) in green table olives of the Manzanilla variety: prepared in the Castelvetrano style and embodiment of the invention according to different examples Chlorophyll pigment (%) Zinc SAMPLE a* with Mg with 2H.sup.+ with Zn.sup.2+ (ppm) Fresh fruit ?12.52 ? 0.01 97.6 ? 2.1 2.4 ? 0.8 3.10 ? 0.25 Initial Castelvetrano ?5.87 ? 0.51 50.1 ? 4.4 49.9 ? 4.4 Nd.sup.1) Castelvetrano 6 months at 4? C. ?2.68 ? 0.42 29.7 ? 15.5 70.3 ? 15.5 Nd STEPS OF THE INVENTION.sup.2) A B C D E F Example 1: 3 steps pH 5 and 3000 ppm (1:3) NO 5 YES P ?7.30 ? 0.51 20.5 ? 1.1 34.6 ? 0.1 44.9 ? 1.2 Nd and pasteurisation pH 5 control without Zn ?0.22 ? 0.57 18.5 ? 0.5 81.5 ? 0.5 (accelerated (1:3) storage test) Example 2: 4 steps pH 4 pH 9.6 (1:3) and Zn.sup.2+ 5 YES P ?1.53 ? 0.25 0.4 ? 0.3 22.0 ? 2.0 74.4 ? 1.4 503.2 ? 34.2 and pasteurisation (1:3) 3000 ppm Example 3: 3 steps pH 9.5 (1:1) and Zn.sup.2+ and pasteurisation 3.1 pH 4 80 ppm NO YES P 0.25 ? 0.32 Nd Nd Nd Nd 3.2 (1:3) 100 ppm 0.30 ? 0.27 3.3 120 ppm ?0.35 ? 0.41 3.4 140 ppm ?0.33 ? 0.28 3.5 Control without Zn.sup.2+ 3.93 ? 0.13 Example 4: 2 steps pH 9.5 (1:1) and Zn.sup.2+ and sterilisation 4.1 pH 4 80 ppm NO NO E ?4.28 ? 0.38 4.7 ? 0.1 45.3 ? 3.6 48.8 ? 4.6 58.8 ? 6.9 4.2 (1:3) 100 ppm ?4.61 ? 0.58 5.3 ? 1.7 51.8 ? 0.3 42.9 ? 3.0 68.5 ? 3.2 4.3 120 ppm ?4.71 ? 0.71 5.3 ? 0.4 44.4 ? 0.9 50.3 ? 0.5 86.2 ? 5.1 4.4 140 ppm ?5.00 ? 0.39 3.1 ? 0.1 50.3 ? 1.1 54.6 ? 1.2 70.4 ? 5.6 Example 5: 2 steps (1:1) and sterilisation pH 9.5 pH 4 (1:1) and Zn.sup.2+ pH 9.5 NO NO E ?3.26 ? 1.53 20.1 ? 1.2 55.7 ? 2.6 23.3 ? 0.8 34.8 ? 1.1 pH 9 100 ppm pH 9 ?2.54 ? 1.51 20.4 ? 1.4 63.1 ? 2.4 15.3 ? 1.0 37.8 ? 5.9 Note: .sup.1)Nd: not determined; .sup.2)A: treatment with buffered acid solution; B: treatment with zinc salt; C: treatment with buffered base solution; D: washes: E: packed in brine; F: heat treatment for conservation; P: pasteurization for 6 min at 80? C.: S: Sterilisation for 43 min at 117? C.

[0075] The results demonstrate that the tested storage conditions can be used to maintain the desired green colour of the olives prepared in the Castelvetrano style and that this improvement of the colour will be intensified as the storage time under these conditions passes. After 6 months of real storage at room temperature, the product has significant improvement in the apparent colour and can be washed, packed and pasteurised for the sale thereof.

[0076] b) Step D: Washes.

[0077] Immersion of the olives in tap water for 60 h, with a change of water every 12 h (5 washes).

[0078] c) Steps E and F: Packing in Treating Brine and Heat Treatment for Preservation.

[0079] Filling of 370 mL glass bottles with approximately 156 g of fruits and 180 mL of a 0.1 M lactic acid/lactate buffer mixture at pH 4 and containing 4% (w/v) of NaCl at a temperature of 70? C. and pasteurisation at 80? C. for 6 minutes.

[0080] The formed zinc metal-chlorophyll complexes, responsible for the improvement of the green colour, are stable and are maintained after heat treatment for pasteurisation. In the product that has remained in treatment for 6 months, the value of the coordinate a* indicated a stabilisation of the green colour (0.27), and also presented a high percentage of zinc metal-chlorophyll complexes (71.63%). However, the long duration of the treatment and the high concentration of zinc salt led to the development of brown patches on the product, thereby making it unacceptable.

Example No. 2: Pasteurised Product Prepared in Four Steps

[0081] 1) Step A: Treatment with Buffered Acid Solution:

[0082] Treatment of green table olives prepared in the Castelvetrano style in a lactic acid/NaOH buffer solution at a concentration of 0.1 M and pH 4, containing NaCl at 4% (w/v), and in a solid/liquid ratio of 1:3 for 9 days, at a room temperature of 25?3? C.

[0083] 2) Steps B and C: Treatment with Zinc Salt in a Buffered Base Solution.

[0084] Immersion of the fruits in a 0.1 M glycine/NaOH buffer mixture at pH 9.5, containing NaCl at 4% (w/v) and the zinc acetate food additive, in a concentration of 3 g/L (3000 ppm) and in a solid/liquid ratio of 1:3, for 6 days, at a room temperature of 25?3? C.

[0085] 3) Step D: Washes.

[0086] Immersion of the olives in tap water for 60 h, with a change of water every 12 h (5 washes).

[0087] 4) Steps E and F: Packing in Treating Brine and Heat Treatment for Preservation.

[0088] Filling of 370 mL glass bottles with approximately 156 g of fruits and 180 mL of a 0.1 M acetic acid/acetate buffer mixture at pH 4.3 and containing 4% (w/v) of NaCl at a temperature of 70? C. and pasteurisation at 80? C. for 8 min.

[0089] With this second example, a first optimisation of the treatment conditions is carried out. It has been demonstrated that the optimal pH for forming the metal-chlorophyll complexes depends on the type of chlorophyll substrate. In the case of chlorophylls and derivatives that contain Mg.sup.2+, the complexing reaction is quicker at acid pH, since these conditions favour the exchange of Mg.sup.2+ for 2H.sup.+ and of 2H.sup.+ for Zn.sup.2+. However, there are bibliographic references that demonstrate that in heat-treated vegetables, where all chlorophyll derivatives are of the pheophytin type (free of Mg.sup.2+), the formation of the complexes with Zn.sup.2+ is intensified at alkaline pH. In this example, steps A and B are carried out separately at different pH values, with the aim of reducing the time of treatment with zinc salt. The fruit is subjected to a first acid treatment at pH 4 to cause the pheophytinisation of the chlorophyll substrates (FIG. 3), followed by a second treatment with buffered base brine at pH 9.5, in the presence of 3 g/L (3000 ppm) of Zn.sup.2+ ions. In only 6 days of treatment with the zinc salt, the formation of 74.37% of zinc complexes (FIG. 3 and Table 1) and a resulting stabilisation of the green colour, measured based on the parameter a*, with a value of ?1.53, is achieved. The fruits are subjected to 5 washes to reduce the content in zinc and finally they are packed in acid brine and pasteurised. The complexes formed are stable to the heat treatment and the green colour remains stable, but the zinc content of the product was 0.5 g/kg (503.22 ppm), exceeding the legally established limits.

Example No. 3: Pasteurised Product Prepared in Three Steps

[0090] 1. Step A: Treatment with Buffered Acid Solution.

[0091] Treatment of green table olives prepared in the Castelvetrano style in a lactic acid/NaOH buffer solution at a concentration of 0.1 M and pH 4, containing NaCl at 4% (w/v), and in a solid/liquid ratio of 1:3 for 9 days, at room temperature of 25?3? C.

[0092] 2. Steps B and C: Treatment with Zinc Salt in a Buffered Base Solution.

[0093] Immersion of the fruits in a 0.1 M glycine/NaOH buffer mixture at pH 9.5, containing NaCl at 4% (w/v) and the zinc acetate food additive in concentrations of 0.08 g/L, 0.1 g/L, 0.12 g/L, and 0.14 g/L (80, 100, 120, and 140 ppm) and in a solid/liquid ratio of 1:1, for 48 h at room temperature.

[0094] 3. Steps E and F: Packing in Treating Brine and Heat Treatment for Preservation.

[0095] Filling of 370 mL glass bottles with approximately 156 g of fruits and 180 mL of a 0.1 M lactic acid/NaOH buffer mixture at pH 4.3 and containing 6% (w/v) of NaCl at a temperature of 70? C. and pasteurisation at 80? C. for 6 minutes.

[0096] In this third example, the amount of the zinc salt used is reduced, which enables the washing step to be eliminated; however, it does not achieve proper stabilisation of the green colour, the values of a* being maintained between 0.30 and ?0.35 based on the amount of added zinc (Table 1).

Example No. 4: Sterilised Product Prepared in Two Phases

[0097] 1) Step A: Treatment with Buffered Acid Solution.

[0098] Treatment of green table olives prepared in the Castelvetrano style in a lactic acid/NaOH buffer solution at a concentration of 0.1 M and pH 4, containing NaCl at 6% (w/v), and in a solid/liquid ratio of 1:3 for 9 days, at a room temperature of 25?3? C.

[0099] 2) Steps B, C, E and F: Packing in Treating Brine at Buffered Base pH, Addition of Zinc Salt and Heat Treatment for Sterilisation.

[0100] Filling of 370 mL glass bottles with approximately 156 g of fruits and 180 mL of the 0.1 M glycine/NaOH buffer mixture at pH 9.5, containing 4% (w/v) of NaCl and the zinc acetate food additive in concentrations of 0.08 g/L, 0.1 g/L, 0.12 g/L, and 0.14 g/L (80, 100, 120, and 140 ppm) and in a solid/liquid ratio of 1:1, leaving a headspace of at least 2 mL. After 48 h in equilibrium, a heating treatment for technical sterilisation is carried out for at least 15 F.sub.0 (43 minutes at 117? C.).

[0101] In this fourth example, an additional optimisation is carried out combining steps B, C and E with a heat treatment for sterilisation. Therefore, the amount of the additive used is reduced to 0.14 g/L (140 ppm), the washes are eliminated, and the total preparation time of the product is reduced. After the treatment step with acid buffer at pH 4 for 9 days, which causes a percentage of pheophytinisation in the chlorophyll substrates of at least 95% (FIG. 3), the fruits are packed in a buffer mixture at pH 9.5, containing different amounts of zinc and they are subjected to heat treatment for sterilisation at 15 F.sub.0. Immediately after the heat treatment, the formation of a high percentage of zinc complexes (>43%) and a stabilisation of the green colour (a* between ?4.28 and ?5.00) is already achieved (FIG. 3 and Table 1). Although all the treatments achieve the desired improvement/stabilisation of the green colour, only the treatments with 0.08 g/L and 0.1 g/L (80 and 100 ppm) of zinc acetate maintain an amount of zinc in the finished product that is less than the legally permitted amount of 0.075 g/L (75 ppm) (Table 1). The product would be ready for the sale thereof in 10 days and unlike the products of this type of preparation of heat-treated olives currently available on the market, the colour can continue to favourably evolve during the storage of the product at room temperature.

Example No. 5: Sterilised Product Prepared in Two Phases

[0102] 1) Steps A and B: Treatment with Zinc Salt in a Buffered Acid Solution.

[0103] Treatment of green table olives prepared in the Castelvetrano style in a lactic acid/NaOH buffer solution at a concentration of 0.1 M and pH 4, containing NaCl at 4% (w/v) and 0.1 g/L (100 ppm) of the zinc acetate food additive. The solid/liquid ratio is 1:1 and the treatment lasts 9 days at a room temperature of 25?3? C.

[0104] 2) Steps C, E and F: Packing in Treating Brine at Buffered Base pH and Heat Treatment for Sterilisation.

[0105] Filling of 370 mL glass bottles with approximately 156 g of fruits and 180 mL of the 0.1 M glycine/NaOH buffer mixture at pHs 9 and 9.5, containing 4% (w/v) of NaCl, in a solid/liquid ratio of 1:1, leaving a headspace of at least 2 mL. After 48 h in equilibrium, a heating treatment for technical sterilisation is carried out for at least 15 F.sub.0 (43 minutes at 117? C.).

[0106] In this fifth example, an additional optimisation is carried out combining steps A and B (treatment in buffered acid solution and treatment with zinc salt). Thus, the amount of zinc that is incorporated in the product is further reduced to <40 ppm (Table 1), forming an amount of zinc metal-chlorophyll complexes that is less than that of the previous example (between 15 and 23%) but enough to stabilise the green colour, with a value of a* between ?2.54 and ?3.26. In this case, by adding zinc in the step of the acid treatment, the degree of pheophytinisation of the chlorophyll pigments was lower, maintaining 20% of the native complexes with magnesium after the heat treatment.