Lactobacillus bulgaricus having decreased acid production and/or improved aroma and flavor production

FIELD OF THE INVENTION
The present invention concerns a Lactobacillus bulgaricus having decreased acid production and/or improved aroma and flavor production.
The present invention is related also to a food composition, especially a mild yoghurt or mild yoghurt like products comprising the Lactobacillus bulgaricus according to the invention.
BACKGROUND OF THE INVENTION AND STATE OF THE ART
Yoghurt results from growth association of the two lactic acid bacteria, Streptococcus thermophilus and Lactobacillus bulgaricus. They grow together in milk where they ferment lactose, which is present at about 40-50 g per liter, to lactate. The whole fermentation usually takes 3 to 5 hours at 40.degree. C. and lowers pH from neutral to about 4.2. Upon storage at 4.degree.-12.degree. C. for several days, the pH then drops further to values below 4.0. Parallel to this increased acidity an appearance of bitterness develops and greatly degrades the organoleptic quality of the product.
It is L. bulgaricus which produces the typical yoghurt aroma during the fermentation process. Therefore, yoghurt missing or having a reduced titer of metabolic active L. bulgaricus cells miss the aroma components of the typical yoghurt. Thus, such yoghurt (or yoghurt like products) can be very neutral, i.e. flat in taste. This problem is particularly eminent for the production of mild or very mild yoghurt, which as a consequence of the limited growth rate of L. bulgaricus tend to lose a lot of their aroma.
The number of consumers that prefer the milder yet aromatic and flavorful yoghurt seems to have increased in recent years. Therefore, the control method of the acid production on the milk fermentation process and the preventing of the post-acidification, which is the pH dropping during the storage, were truly desired by yoghurt producers. Up to now, several methods or starter strain improvements have been suggested to control the acidification and post-acidification of yoghurt. Most of them are to reduce the number of the active cells in starter culture or to eliminate living cells from the finished product by pasteurizing. Alternatively, low acidifying strains are being used.
U.S. Pat. No. 4,734,361 (Murao et al.) describes such a Lactobacillus bulgaricus strain (OLL 1074) which has been deposited in Japan under the number FERM BP 1041.
This variant shows a weak tendency towards formation of lactic acid at lower temperatures.
By employing this variant, it is possible to produce a fermented milk or lactic acid beverage in which post-acidification at a lower temperature is reduced.
U.S. Pat. No. 5,071,763 (Somkuti et al.) describes that mutant strains of Streptococcus thermophilus having defective lactose transport systems and having a phenotype gluS, lacS-, sucS+ and .beta.gal+ are effective for use in processes where the hydrolysis of lactose is important. Thermostability of these strains as well as production of .beta.-gatactosidase allow lactose hydrolysis prior to and during pasteurization. These organisms provide the food industry with improved methods of making reduced lactose dairy products.
In L. bulgaricus, lactose is taken up by the lactose permease system and cleaved by the .beta.-galactosidase into its two moieties, glucose and galactose. Glucose is metabolized further to pyruvate, most of which is converted to lactate by the D-lactate dehydrogenase (D-LDH).
However, some of the pyruvate is decarboxylated to acetaldehyde, an important yoghurt aroma component, or channeled into other pathways resulting in aroma or aroma precursor elements.
Thomas et al. (J. of Bacteriology, May 1974, p. 329-333) and Smart et al. (Applied and Environmental Microbiology, March 1987, p. 533-541) describe that for Lactic streptococci, homolactic fermentation can be changed to heterolactic fermentation by reducing the LDH activity.
Payton et al. (FEMS Microbiology letters, 26, 1985, p. 333-336) describe that the LDH minus mutant of Bacillus stearothermophilus increase the amount of the ethanol production (following fermentation of glucose), whereas they lose the ability to produce lactate.
The document Journal of Bacteriology (vol. 144; no. 1, 1980, pages 217-221) shows that when the strain Lactobacillus bulgaricus NLS-4 grows anaerobically in continuous culture with limiting glucose, a shift in the pH of the medium from the acidic to the alkaline range causes this normally homofermentative bacterium to catabolize glucose in a heterofermentative fashion. The change in the fermentation is accompanied by a decrease in lactate dehydrogenase (LDH) biosynthesis in alkaline conditions.
However, yoghurt is an acid medium and this document does not suggest that it is possible to obtain a decrease in lactate dehydrogenase biosynthesis in acid conditons.
SUMMARY OF THE INVENTION
The present invention aims to provide a Lactobacillus bulgaricus having improved aroma and flavor production.
Another aim of the present invention is to provide a Lactobacillus bulgaricus also having reduced acidification and post-acidification.
A further aim of the present invention is to obtain a food composition, preferably a mild yoghurt or a mild yoghurt like product comprising said Lactobacillus bulgaricus, having an increased aroma and flavor production and/or a reduced acidification and post-acidification, preferably at low and high temperature.
DETAILED DESCRIPTION OF THE INVENTION
The present invention concerns a Lactobacillus bulgaricus having a more reduced lactate dehydrogenase (LDH) activity than of the wild type strain Lfi5 (deposited under the name CNCM I-800 at the Institut Pasteur, 28 rue du Docteur ROux, 75024 PARIS Cedex 15, FRANCE).
Advantageously, said lactate dehydrogenase activity is lower than 50%, preferably lower than 10%, of the lactate dehydrogenase activity of this wild type strain.
Advantageously, the lactate dehydrogenase activity is lower than 250 units, preferably lower than 150. units, of enzyme activity/10 ml culture.
The lactate dehydrogenase activity is measured by the following decrease in absorbance at 340 nm due to conversion of NADH to NAD.sup.+ in 1 ml of reaction mixture, 8 mM sodium pyruvate, 0.15 mM NADH, 50 mM tris-chloride pH 7.5. One unit of enzyme activity is defined as that amount which oxidized 1 .mu.mole of NADH per minute at 25.degree. C.
The Lactobacillus bulgaricus according to the invention is also characterized by a more increased .beta.-galactosidase (.beta.-gal) activity than of the wild type strain Lfi5.
Advantageously, said .beta.-galactosidase activity is higher than 200%, preferably higher than 500% of the .beta.-galactosidae activity of the wild type strain Lfi5.
Advantageously, the .beta.-galactosidase activity is higher than 300 units, preferably higher than 500 units of enzyme activity/10 ml culture.
The .beta.-galactosidase activity is determined by the method of Miller J. H. (Experiments in molecular genetics, Cold Spring Harbor Laboratory N.Y., 1972).
50 .mu.l of cell free extract is added in 1 ml of Z buffer, 0.1.M sodium phosphate pH 7.0, 10 mM KCl, 1 mM MgSO.sub.4, 50 mM 2-mercaptoethanol, and equilibrated at 28.degree. C. Prewarmed 200 .mu.l ONPG is added and incubated at 28.degree. C. for 20 minutes. The reaction is stopped by adding 0.5 ml Na.sub.2 CO.sub.3 1M.
The absorbance at 420 nm is measured. One unit of enzyme activity is defined as the amount that hydrolyzed 1 .mu.mole of ONPG per minute at 28.degree. C.
Preferably, the Lactobacillus bulgaricus according to the invention is characterized by a LDH activity versus .beta.-galactosidase activity lower than 0,8; preferably lower than 0,3.
The Lactobacillus bulgaricus according to the invention (isolated mutants) presents pathways which direct more of the pyruvate towards the aroma pathways than the production of lactic acid.
Preferably, the Lactobacillus bulgaricus according to the invention is selected from the group consisting of the strains of Lactobacillus bulgaricus CNCM I-1348 and I-1349.
The strains are characterized by the following properties:
Origin: mutant isolated from a commercialized L. bulgaricus strain of the Nestle collection;
Morphology: straight unflagellated Bacilli. No sporulation, Gram.sup.+ microorganisms, catalase negative and optionally anaerobics;
Saccharide fermentation: lactic acid production from:
D-glucose
D-fructose
D-mannose
lactose;
Miscellaneous:
reduced activity of the LDH enzyme (lactate dehydrogenase)
texturating properties (exopolysaccharide production).
Mutants of Lactobacillus bulgaricus having reduced LDH activity will increase the production of aroma and flavor compounds. Analysis of the isolated mutants by comparing their LDH versus .beta.-galactosidase activity (LDH/.beta.-gal ratio) indicated which of the mutants are not only low in LDH activity (high production of aroma compound and low production of lactic acid) but in fact channeled more of the carbon flow (.beta.-galactosidase activity) into the production of aroma and flavor compounds.
The present invention concerns also a food composition comprising said Lactobacillus bulgaricus.
Advantageously, the said food composition is a yoghurt or yoghurt like product, preferably a mild yoghurt or mild yoghurt like products, comprising the Lactobacillus bulgaricus according to the invention and Streptococcus thermophilus.
The yoghurt or the yoghurt like product according to the invention are characterized by an increased aroma and flavor production and a reduction of acidification and post-acidification.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 represents the growth behaviors (.circle-solid. OD 600, .gradient. LDH/protein.times.100, .tangle-soliddn. LDH/.beta. gal) of the L. bulgaricus Lfi5.
FIG. 2 represents the growth behaviors of LDH low mutants on Lfi5 (.largecircle. Lfi 5, .circle-solid. KTL50, .gradient. KTL6, .tangle-soliddn. KTL8, .quadrature. KTL52, .box-solid. KTH1).
FIG. 3 represents the effects of LDH in the medium to KTL 50 (.largecircle. KTL50 without LDH, .circle-solid. KTL50 with LDH).

DESCRIPTION OF A PREFERRED EMBODIMENT OF THE INVENTION
A. Optimization of mutagenesis on Lactobacillus bulgaricus Media and bacteria
Lactobacillus bulgaricus is grown in 10 ml Lactobacillus MRS broth (0.5% yeast extract, 1% meat extract, 1% peptone, 0.1% Tween 80, 0.2% ammonium citrate, 0.5% sodium acetate, 0.2% K.sub.2 HPO.sub.4, 0.01% MgSO.sub.4, 0.005% MnSO.sub.4) (x) at 42.degree. C. MRS agar plate contains MRS with 15 g agar per 1 liter. MRS X-Gal agar plates contains X-Gal(5-bromo-4-chloro-3-indolyl-.beta.-D-galactopyranoside) at 25 .mu.g/ml.
The Mutagenesis of L. bulgaricus strain Lfi5 are obtained with ultraviolet light Mutagenesis or by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) mutagenesis according to the method of Silhavy (T. J. Silhavy, M. L. Berman and W. Enquist (1984), Experiments with gene fusions: Cold Spring Harbor Laboratory).
Mutation frequency of MNNG mutagenesis is 7 times higher than that of UV light mutagenesis.
B. Screening of low activity mutants of lactate dehydrogenase
Overnight cultures of mutagenized cells are diluted and plated onto MRS agar plate and incubated at 42.degree. C. overnight. Single colonies are picked, inoculated in 250 .mu.l MRS broth in microtites plates (FALCON 3072) and grown at 42.degree. C. overnight. 50 .mu.l of each cell suspension are dot-blotted onto membrane filter (Dupont GeneScreen). The filter is placed on 3M Whatman filter saturated with the cell lysis solution, 1 mg/ml lysozyme and 50 .mu.g/ml mutanolysin in water, and incubated at 37.degree. C. for 30 min. Then the filter is exposed in chloroformvapor for 30 minutes, airdried and frozen at -80.degree. C. for 30 minutes. It is washed with 50 mM tris-chloride buffer pH 8.0 to remove cell debris. The washed filter is soaked for 1-4 minutes in staining solution, 134 mM D-lactic acid sodium salt, 2 mM iodonitrotetrazolium chloride, 1.4 mM NAD.sup.+, 0.5 mM N-methylphenazonium methyl sulfate, 50 mM trischloride pH 8.0. To stop the reaction, the filter is washed with 0.1N HCl. The activity of the Lactate dehydrogenase is relative to the intensitivity of the red coloring of the individual colonies on the plates. Cells showing weak signals are transfered to 10 ml fresh MRS broth and incubated at 42.degree. C. overnight. The cells are harvested by centrifugation and resuspended in 1 ml MRS broth containing 15% glycerol. Cell suspensions are stored at -80.degree. C.
Preparation of cell free extracts
Prewarmed 10 ml fresh MRS broth containing 2% lactose is inoculated with 2% of an overnight culture and incubated at 42.degree. C. for 7 hours. The cells are harvested by centrifugation and washed twice with the buffer, 50 mM trischloride pH 8,0, 100 mM NaCl, 2 mM EDTA, 1 mM PMSF, 1 mM DTT and resuspended in 1 ml of the buffer. 100 .mu.l of 10 mg/ml lysozyme solution and 50 .mu.l of 1 mg/ml mutanolysin solution are added and incubated at 37.degree. C. for 10 minutes. Cell debris is removed by centrifugation at 12,000 rpm for 30 minutes.
Lactate dehydrogenase assay
Lactate dehydrogenase activity is measured by the following decrease in absorbance at 340 nm due to conversion of NADH to NAD.sup.+, in 50 mM tris-chloride pH 7.5. One unit of enzyme activity is defined as the amount with oxidized 1 .mu.mole of NADH per minute at 25.degree. C.
.beta.-galactosidase assay
.beta.-galactosidase activity is determined by the method of Miller (Experiments in molecular genetics, Cold Spring Harbor Laboratory N.Y., 1972). 50 .mu.l of cell free extract is added in 1 ml of Z buffer, 0.1M sodium phosphate pH 7.0, 10 mM KCl, 1 mM MgSO.sub.4, 50 mM 2-mercaptoethanol, and equilibrated at 28.degree. C. Prewarmed 200 .mu.l ONPG is added and incubated at 28.degree. C. for 20 minutes. The reaction is stopped by adding 0.5 ml 1M Na.sub.2 CO.sub.3. Absorbance at 420 nm is measured. One unit of enzyme activity is defined as the amount that hydrolyzed 1 .mu.mole of ONPG per minute at 28.degree. C.
Protein assay
Total protein concentration is determined by the dye binding assay of Bradford (M. M. Bradford, (1976), Anal. Biochem, 72: 248-254) using the kit of Bio-Rad.
Lactobacillus bulgaricus, Lfi5 and YL30 are mutagenized as described before (Table 1). 3388 colonies of MNNG mutagenized cells of Lfi5, 616 colonies of UV mutagenized cells of Lfi5 and 1078 colonies of MNNG mutagenized cells of YL30 are picked up and tested. 152 colonies are identified as LDH mutants in this first screening with the membrane assay. FIG. 1 presents an example of such a result.
Candidates identified in this screening are used to measure the LDH activity. Each candidate is grown in MRS with 2% lactose media, and harvested at the early stationary log-phase that provide the highest activity. The cells are lysed by incubation with mutanolysin and lysozyme. Other methods are tested as well. They are summarized in Table 2. The glass beads method is described by Abbondi (M. E. Abbondi, S. Pandian, G. Trepanier, R. E. Simard and B. H. Lee (1991), J. Food Sci., 56: 948-953).
The activity of LDH is determined by the specific activity of total LDH units per total cellular protein of the cell free extract. The specific activity of LDH is continuously increased with the cell growth (FIG. 2). Since .beta.-galactosidase is also an important enzyme of the glycolysis pathway, the ratio LDH per .beta.-galactosidase activity should be constant. In fact, the ratio is almost stable from the mid-log phase to the early stationary phase. The mutants are identified by the evaluation of this ratio, total LDH versus .beta.-galactosidase activity. The results are shown in Table 3.
The mutants are classified in six groups. The mutants of Group 1 indicate low total LDH activity, below the average minus 20%, but keep the normal level of .beta.-gal activity. Their low LDH / .beta.-galactosidase ratio is only due to the low LDH mutations. Group 2 also has low LDH activity, but their .beta.-gal activity is more than the average of the wild type.
The mutants in Group 1, 2, 3 and 4 are the low LDH mutants. They have low LDH / .beta.-galactosidase ratios and low total LDH activities. 13 mutants of Lfi5 and 10 mutants of YL30 are categorized in these groups. The frequency of mutation for each strain is 3.8.times.10.sup.-3 and 8.3.times.10.sup.-3 respectively.
KTL50, 78, 81, KTY41, 18 and 46 have lower LDH / .beta.-galactosidase ratios (1:100 to 1:200) than the wild type strain. Moreover, their total .beta.-gal activity is conserved.
Mutants of Group 5 show normal activity. However, their .beta.-gal activity is increased.
KTL50 and KTH1 of Group 1, KTL6 of Group 2, KTL52 of Group 3 and KTL8 of Group 5 are examined for growth behavior and post acidification.
C. Characterization of LDH low mutants Acidification of LDH low activity mutants
Growth Curve
Mutants are inoculated at 2% in pyrex culture tubes (16.times.150 mm) containing 17 ml prewarmed MRS with 2% lactose and incubated at 42.degree. C. The optical density at 550 nm are monitored every 30 minutes.
pH curve
Mutants are inoculated at 2% in 10 ml prewarmed MRS broth with 2% lactose and incubated at 42.degree. C. pH is monitored every 30 minutes.
Post-acidification of LDH low activity mutants in mixed culture yoghurt assays
The starter culture inoculum consists of 1.5% Sfi16, 1.5% Sfi21 standard commercial strains of S. thermophilus and 0.8% of the candidate L. bulgaricus. Yoghurts are prepared from 150 ml pasteurized milk, 3% reconstituted skim milk 1.5% milk fat, inoculated with the above mixed culture. The cultures are grown at 40.degree. C. until they reach a pH value of about 4.6. They are then cooled to 4.degree. C. overnight and stored at 4.degree. C. or 12.degree. C. for 26 days. The pH value, organoleptic qualities and cell numbers are monitored after 7 days, 14 days and 26 days of incubation.
The results are shown in Table 4. Yoghurt stored at 4.degree. C. shows only weak post-acidification after 26 days. Mutants and wild type strain kept their pH value above 4.3. There are small differences of pH value (about 0.1) between wild types and LDH low mutants. The culture stored at 12.degree. C. shows post-acidification. While wild type strain Lfi5 acidifies the pH value to 4.0 after 26 days, the pH of LDH low mutants, KTL50 and KTH1, are still kept at 4.2.
The KTL1, 18 and 42 Lactobacillus bulgaricus strains are filed according to the Budapest treaty in the Collection Nationale de Cultures de Microorganismes (CNCM), Institut Pasteur, 28, rue du Docteur Roux, 75024 Paris Cedex 15, France, under the numbers CNCM I-1348, CNCM I-1349 and CNCM I-1350.
The invention will be illustrated by the following examples.
Example I
Yeast extract (0.1% v/v) was added to 500 ml 9% (w/v) skim milk powder. The resulting solution was autoclaved at 121.degree. C. for 15 minutes, followed by addition of 10% (v/v) of an active culture of L. bulgaricus strain CNCM I-1348 (KTL 1) containing about 5.times.10.sup.8 bacteria/cm.sup.3.
By incubating this mixture for 4 hours at 40.degree. C., a leaven containing around 2.5.times.10.sup.8 microorganisms/cm.sup.3 is obtained.
According to the same method, a leaven containing around 5.times.10.sup.8 thickening S. thermophilus/cm.sup.3 from an active culture of a commercialized strain is obtained.
Skim milk powder (3% w/v) was added to a milk standard batch containing 1.5% fat. The resulting solution was pasteurized for 30 minutes at 90.degree. C., followed by addition of 1% (v/v) of the L. bulgaricus strain CNCM I-1348 (KTL 1)leaven and 3% (v/v)of the commercialized strain of S. thermophilus.
After a weak stirring, the preparation is disposed in cans and incubated for 4h20 at 40.degree. C. until a pH of 4.62.
The yoghurt obtained presents a good texture and a very interesting taste for this type of product. Around 1.times.10.sup.9 S. thermophilus/cm.sup.3 and around 1.times.10.sup.8 L. bulgaricus/cm.sup.3 are numbered.
Example II
As in Example 1, a leaven of L. bulgaricus CNCM I-1349 (KTL 18) is prepared, containing around 3.times.10.sup.8 microorganisms/cm.sup.3 after 8 hours after incubation.
With the addition of 1% of a L. bulgaricus CNCM I-1349(KTL 18) leaven, and 3% S. thermophilus leaven to a standard milk batch (as described in Example 1), a yoghurt of pH 4.61 is obtained.
After 4h40 of incubation at 40.degree. C., around 8.times.10.sup.8 S. thermophilous and around 1.times.10.sup.7 L. bulgaricus/cm.sup.3 are numbered.
This yoghurt of very unctuous texture presents a very interesting fresh milk taste.
Example III
The strain of L. bulgaricus CNCM I-1350 (KTL 42) is obtained according to the process described in the above examples.
After 5 hours, a leaven containing around 5.times.10.sup.8 microorganisms/cm.sup.3 is obtained.
According to the example I, a yoghurt of pH 4.62 is obtained after 3h45 incubation. Around 1.times.10.sup.9 S. thermophilus/cm.sup.3 and around 2.times.10.sup.8 L. bulgaricus/cm.sup.3 are numbered.
In addition of a very sweet texture, it presents a very strong typical yoghurt taste.
These products are submitted to a taste preservation test at 4.degree. C. and 12.degree. C., said tests comprising a pH testing and taste testing after respectively 1, 7, 14 and 26 stockage days.
These results are presented in table 5.
Comparative test
As witness, the original strain of the three mutants CNCM I-1348, CNCM I-1349 and CNCM I-1350 (KTL 1, 18, 42) is used to obtain a yoghurt according to the method described in Example I.
After 3h45 of incubation, a yoghurt with a pH of 4.54 and containing around 1.times.10.sup.9 S. thermophilus/cm.sup.3 and around 2.times.10.sup.8 L. bulgaricus/cm.sup.3 is obtained.
TABLE 1______________________________________Results of the screening of the low LDH mutants Method of Total cell After first After theStrain Mutagenesis number screening second test______________________________________Lfi5 MNNG 3388 99 13 (3.8 .times. 10.sup.-3)Lfi5 UV 616 7 0 (0)YL30 MNNG 1078 46 10 (9.3 .times. 10.sup.-3)______________________________________
TABLE 2______________________________________Comparisons of the cell lysis methodsMethod of Total LDH U/10 ml Total .beta.-gal U/10 mlcell lysis culture culture______________________________________Mutanolysin + 1 213.9 327.8Lysozyme 2 214.5 319.0 Ave 214.7 323.4Glass beads 1 192.6 338.2 2 125.8 203.3 Ave 159.2 270.8Toluene 1 20.8 144.2 2 62.75 312.5 Ave 41.8 228.4______________________________________
TABLE 3.1______________________________________List of mutant on Lactobacillus bulgaricus Lfi5 LDH/ LDH U/10 Gal U/10 OD 550 atStrain name Gal ml cul. ml cul. Havest.______________________________________Lfi5 0.426 229 541 1.23Group 1(Low LDH)KTL50 0.0013 0.5 412 0.82KTL78 0.031 11 359 1.12KTL81 0.035 14 402 1.11KTL83 0.102 52 509 1.16KTH1 0.300 110 368 1.12Group 2 (LowLDH, high .beta.-gal)KTL6 0.233 159 666 1.17KTH16 0.214 129 607KTH18 0.295 172 583Group 3 (LowLDH, low .beta.-gal)KTL52 0.159 17 106 0.65KTL53 0.288 52 182 0.94KTH5 0.300 12 40KTH4 0.256 66 259KTH7 0.294 78 266Group 4(High .beta.-gal)KTL8 0.213 217 1020 0.79KTL65 0.256 201 789 1.35KTL55 0.301 194 644 1.30KTH14 0.277 216 780KTH17 0.297 221 744Group 6 5.1213 182 36(Low .beta.-gal)KTL69______________________________________
TABLE 3.2______________________________________List of mutants on Lactobacillus bulgaricus YL30 LDH/ LDH U/10 Gal U/10 OD 550 atStrain name Gal ml cul. ml cul. Havest.______________________________________YL30 0.314 181 574 1.30Group 1(Low LDH)KTY41 0.0002 0.2 650 1.00KTY18 0.007 3 441 0.91KTY46 0.0023 11 467KTY1 0.102 46 454KTY4 0.170 106 625KTY19 0.172 113 659KTY11 0.198 112 567Group 2 (LowLDH, high .beta.-gal)KTY7 0.141 101 717 1.40KTY9 0.163 149 916Group 4 0.182 173 952 1.10(High .beta.-gal)KTY13Group 5 (Low 0.982 60 61 0.67LDH, Low .beta.-gal)KTY28Group 6 278.8 175 0.6(Low .beta.-gal)KTY8______________________________________
TABLE 4______________________________________Post acidification of yoghurt cultures pH value after: at 4.degree. C. 12.degree. C.Strains Incubation.sup.(1) 7 days 14 days 26 days Cells.sup.(2)______________________________________Lfi5 3 h 35 4.40 4.34 4.32 4.0 .times. 10.sup.7 4.20 4.06 4.05 9.0 .times. 10.sup.7KTL50 4 h 4.53 4.43 4.42 1.6 .times. 10.sup.7 4.28 4.15 4.17 6.4 .times. 10.sup.7KTH1 4 h 20 4.46 4.33 4.35 7.5 .times. 10.sup.7 4.26 4.12 4.14 1.8 .times. 10.sup.8KTL6 3 h 10 4.51 4.39 4.37 6.3 .times. 10.sup.7 4.20 4.05 4.02 7.3 .times. 10.sup.7KTL8 4 h 45 4.32 4.37 4.42 2.0 .times. 10.sup.5 4.26 4.22 4.24 3.5 .times. 10.sup.6KTL18 4 h 40 4.54 4.54 4.59 9.4 .times. 10.sup.6 4.38 4.24 4.25 3.4 .times. 10.sup.6______________________________________ .sup.(1) Incubation time to reach pH 4.6: The yoghurt was then transferre and stored at 4 or 12.degree. C. .sup.(2) Cell counts of L. bulgaricus per ml yoghurt culture after 26 day
TABLE 5______________________________________ T.degree. = 4.degree. C. T.degree. = 12.degree. C.Example Stockage pH degustation pH degustation______________________________________1 1 day 4.46 Sweet, 4.46 Sweet, flavoring flavoring 7 days 4.46 Sweet, 4.26 Acid taste flavoring 14 days 4.33 Sweet, fresh 4.12 Acid 26 days 4.35 Sweet, fresh 4.14 Raw milk taste2 1 day 4.65 Sweet, light 4.65 Sweet, light taste taste 7 days 4.65 Sweet, light 4.38 Sweet, fresh taste milk 14 days 4.54 Sweet, light 4.24 Very sweet, taste fresh 26 days 4.59 Sweet, light 4.25 Very sweet, taste fresh and tasting of wood fruit3 1 day 4.58 Sweet, light 4.58 Sweet, light 7 days 4.48 Sweet, light 4.22 Sweet, strong yoghurt taste 14 days 4.36 Sweet, 4.07 Acid, lightly strong taste bitter 26 days 4.38 Sweet, 4.07 Acid, bitter strong tasteWITNESS 1 day 4.45 Sweet, 4.45 Sweet, lightly bitter lightly bitter 7 days 4.40 Sweet, light 4.22 Sweet, strong yoghurt taste 14 days 4.36 Sweet, 4.07 Acid, lightly strong taste bitter 26 days 4.38 Sweet, 4.07 Acid, bitter strong taste______________________________________
The above examples show that mutants CNCM I-1348, CNCM I-1349 and CNCM I-1350 (KTL 1, 18 and 42) presenting a reduced LDH activity, can produce a yoghurt with very interesting texture, flavoring and post-acidification properties. In addition, very different tastes at very high pH can be obtained.

Number	Name	Date
4411991	Hirrakawa et al.	Oct 1983
4560661	Katsumata et al.	Dec 1985
4605622	Hasegawa et al.	Aug 1986
5382438	Hottinger et al.	Jan 1995
5416020	Severson et al.	May 1995

Lactobacillus bulgaricus having decreased acid production and/or improved aroma and flavor production

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