Proliferation of Bifidobacterium L80 under different proportions of milk protein hydrolysate.

The intestinal microecological environment is critical to an infant's growth. For those infants consuming milk power, it is very important to improve the intestinal microecological environment to promote the healthy growth of infants. In this paper, Milk protein hydrolysate (MPH), consisting of different proportions of proteins and small molecule peptides (5:5, 4:6, 3:7, 2:8, 1:9) were added to infant formula powder (IFP). The effects of MFP-enriched IFP addition on proliferation and metabolism of Bifidobacterium L80 were studied. Compared with MPH-free IFP, MFP-enriched IFP with 1:9 of proteins to small molecule peptides significantly enhanced the proliferation of Bifidobacterium L80, resulting in higher cell density, greater viable counts and higher titratable acidity. MFP-enriched IFP increased the content of seven organic acids and H2O2 in the system, and improved the antibacterial activity to E. coli BL21. This study suggested that MPH could be an effective addition to infant formula powder to promote the growth of Bifidobacterium, so to improve the intestinal health of infants.

Introduction

Neonatal intestinal colonization, a critical stage for an infant’s future physiological health, is beneficially influenced by breastfeeding [38]. Breast milk contains all the nutrients and microbial flora that an infant needs. In cases of breastfeeding insufficient or impossible, cow mike is often used as an alternative. However, cow milk does not contain probiotics. It is of industrial significance to develop formula milk powder which is beneficial to the establishment and increment of infant intestinal flora.

Bifidobacterium is a critical constituent of the human microbiome and plays important a role in digestion and gut immunity, which can benefit the host by improving the balance of intestinal microbes and bring health benefits [6, 8]. Infant’s gut microbiota, which plays a critical role in early life [9], is rich in Bifidobacterium [26], when Bifidobacteria are deficient in the gut, stimulation of their proliferation is required. Recent researches have investigated the effects of oligosaccharides [41], polysaccharides [15], peptides [24, 46], unsaturated fatty acids [30], cyanidin rutinoside [17, 31] on the proliferation and metabolisation of Bifidobacteria.

Research has shown that ɑ-Lactalbumin [2], β-lactoglobulin [45], lactoferrin [28], κ-casein [43] and other proteins or peptides can promote Bifidobacteria growth [20]. In particular, it has been reported that MPH containing short peptides [33] could improve the Bifidobacteria content in foods containing probiotics. However, the effect of the mixture of peptides (as determined by the extent of hydrolysis of the protein precursors) on the proliferation and metabolism of Bifidobacteria is unknown.

Bifidobacterium has an important inhibitory effect on Listeria monocytogenes, Clostridium, staphylococcus, Enterococcus faecalis and Bacillus [1, 27, 35]. Bifidobacterium display a wide range of antimicrobial activities. Besides the production of lactic acid and acetic acid, it also produces fatty acids, hydrogen peroxide, diacetyl and other substances, which play antibacterial role [1, 29].

In conclusion, the increment and antibacterial activity of Bifidobacterium can promote the intestinal functional development of infants to some extent. The object of this research was to assess the influence of the MPH infant formula on the proliferation and metabolism of Bifidobacterium L80, and the inhibition of Escherichia coli BL21. To lay a foundation for the development of infant formula milk powder conducive to healthy intestinal construction.

Materials and methods

Reagents and materials

Whey protein was obtained from Zhengzhou Jiangda Biological Technology Co., Ltd (Zhengzhou, China). Casein was obtained from Beijing Aoboxing Biotechnology Co., Ltd., (Beijing, China). Alcalase® 2.4 L FG 208000 U/g, Sigma Chemical Co., St. Louis, MO, USA was preserved at − 4 °C. Bifidobacterium L80 were provided by the Laboratory of Harbin University of Commerce. Commercially available IFP for comparison was purchased from Wandashan Dairy Co., Ltd.,(Harbin, China).

Analytical standard-grade acids were obtained from Germany (Dr. Ehrenstorfer Gmb-H). Stock standard solutions were prepared by dissolution of acids in Milli-Q® (generated by use of a Milli-Q® system from Millipore (Milford, MA, USA)); all solutions were stored at 4 °C and were used within 1 month. Working standard solutions were prepared daily by dilution with Milli-Q®. Metaphosphoric acid and methanol were chromatographic-reagent grade and obtained from Merck (Sartorius, Gettingen, Germany). Whatman cellulose membrane filters (0.45 µm) were obtained from Millipore Co., USA.

Preparation of whey protein and casein hydrolysate

Milk protein hydrolysates (MPH) with different ratios of protein to peptide were prepared by adjusting the amount of added enzyme. The whey protein and casein powder were mixed into deionized water to make a solution of whey protein and casein at a concentration of 5% w/v. The temperature was set to 50 °C for the hydrolysis and the pH was adjusted to 8.5 by solution of 2 M NaOH. Alcalase® was added at varying ratios (1000U/mL, 1500U/mL, 2000U/mL, 2500U/mL, 3000U/mL) to the mixture of whey protein and casein. After 4 h, the solution was heated to 95 °C and kept for 10 min to kill enzyme, and then was cooled down to room temperature. Then the pH was readjusted to 7 with 2 M NaOH. The hydrolysates were centrifuged at 7000 r/min for 30 min. The resulting milk protein hydrolysate was under freeze drying and was cryopreserved for later usage as supplementation of the IFP. The infant formulation powder was prepared according to the “National Food Safety Standard for Infant Formula Food”. MPH was mixed with IFP at a ratio of 12% (w/w) to provide MPH-enriched IFP with different proportions of proteins and peptides (5:5, 4:6, 3:7, 2:8, 1:9 w/w).

Analytical methods

Determination of growth of Bifidobacterium L80

MPH-enriched IFP with different proportion of protein and peptide (5:5, 4:6, 3:7, 2:8, 1:9 W/W) were added to MRS medium as the experimental group. MPH-free IFP were used as a blank group, the commercial IFP were used as a control group. The mixture was sterilized at 121℃ for 15 min. Bifidobacterium L80 was inoculated into the experimental group, the blank group and the control group were placed in a 37℃incubator for cultivation for 24 h. The viable count was implemented by plate-counting method [5].

The turbidimetric method was used to measure the growth of Bifidobacterium L80. Every 4 h (0 h, 4 h, 8 h, 12 h, 16 h, 20 h, 24 h), the optical density at 600 nm (OD600) was measured for cell growth using a spectrophotometer (UV-1600PC) [40].

Determination of metabolites

Determination of titration acidity

Titration acidity was measured according to Trinder [40]. During the growth of the Bifidobacterium L80, the titration acidity of the fermentation broth was measured at 0 h, 4 h, 8 h, 12 h, 16 h, 20 h and 24 h respectively. Phenolphthalein was used as indicator. The Bifidobacterium fermentation broth was titrated with 0.1 M NaOH to reddish color, and the red color did not disappear within 30 s. Acidity value (°T) is calculated based on the consumption of NaOH solution.

Determination of the inhibitory ratio of Bifidobacterium L80 to E. coli

The inhibitory ratio of Bifidobacterium L80 culture on E. coli was measured at 24 h culturing using the Oxford cup method [36]. E. coli was used as indicator bacteria. Bifidobacterium L80 of the experimental group, blank group and control group were cultured for 48 h, and then injected into Oxford cup for 24 h at 37 ℃. The size of inhibition zones was measured.

Identification of organic acids by HPLC

The MPH group was used as sample group, MPH with 1:9 proportion of macromolecules to small molecule peptides was added to the basic MRS medium. The milk protein group was used as control group, milk protein was added to the basic MRS medium. The basic MRS medium was used as blank group. During the growth of the Bifidobacterium L80 in different groups, Organic acid (Formic acid, Malic acid, Acetic acid, Tartaric acid, Lactic acid, Citric acid) metabolized by Bifidobacterium L80 from the sample group, the blank group, the control group were measured by HPLC at 0, 12, 24, 36, 48, 60, and 72 h.

A HPLC system (Waters® 2695, USA), the parameters of the experiment were as follows: photodiode array detector (Waters® 2489), Agilent ZORBAX SB-C18 column (250 × 4.6 mm, 5 µm), Empower® Chromatography Workstation software. Meanwhile, isocratic elution program (0.1% v/v H3PO4 and methanol) with a flow rate of 1 mL/min was used in this test. Absorbance was monitored at 210 nm and the sample injection volume was 10 μL.

Determination of the hydrogen peroxide content

In acidic environment, hydrogen peroxide reacts to with titanium ions to form an orange complex. The amount of hydrogen peroxide in the sample is then determined by titanium salt spectrophotometry at 430 nm [23]. 10 mL samples and 5 mL titanium ions were transferred to a colorimetric tube, water was added to colorimetric tube to 25 mL. The solution was shaded well and then left still for 10 min. The blank group was replaced with water. The absorbance value was measured at 430 nm.

Statistical analysis

Data were processed and plotted using Excel 2010. The results were analysed using SPSS 17.0 software. All experiments were conducted in triplicate. Analysis of variance (ANOVA) and minimum significant difference (LSD) were performed on the data (P < 0.05).

Results and discussion

Proliferation assessment of Bifidobacterium L80 with proteins and small molecule peptides

The effects of different ratios of protein to small molecule peptide on the 600 nm optical density (OD600) and the viable count of Bifidobacterium L80 are shown in Table 1 and Fig. 1, respectively.

Table 1

Change of optical density (OD) value in the control and mixtures of infant formula containing different proportion of macromolecules and small molecule peptides in MPH

Macromolecules/small molecule peptides	0 h	4 h	8 h	12 h	16 h	20 h	24 h
Blank	0.071 ± 0.019Aa	0.128 ± 0.070Ba	0.344 ± 0.080Ca	0.619 ± 0.086Da	0.687 ± 0.073Ea	0.696 ± 0.079Ea	0.700 ± 0.038Ea
5:5	0.073 ± 0.018Aa	0.128 ± 0.069Ba	0.349 ± 0.075Cb	0.748 ± 0.084Db	0.881 ± 0.121Eb	0.894 ± 0.745Ea	0.890 ± 0.062Eb
4:6	0.071 ± 0.010Aa	0.128 ± 0.047Ba	0.348 ± 0.047Cb	0.791 ± 0.062Dc	0.919 ± 0.067Eb	0.922 ± 0.841Eb	0.922 ± 0.130Eb
3:7	0.079 ± 0.013Aa	0.131 ± 0.074Ba	0.349 ± 0.082Cb	0.858 ± 0.084Dd	0.955 ± 0.105Eb	0.959 ± 0.110Eb	0.960 ± 0.129Ebc
2:8	0.071 ± 0.015Aa	0.133 ± 0.047Ba	0.343 ± 0.028Ca	0.873 ± 0.106Dd	0.990 ± 0.068Ec	0.979 ± 0.103Ec	0.999 ± 0.097Ec
1:9	0.070 ± 0.020Aa	0.145 ± 0.036Bb	0.356 ± 0.097Cc	0.951 ± 0.103De	1.073 ± 0.096Ee	1.073 ± 0.123Ed	1.079 ± 0.080Ed
Control	0.071 ± 0.010Aa	0.232 ± 0.083Ba	0.352 ± 0.027Cb	0.902 ± 0.133Dd	0.917 ± 0.100Eb	0.922 ± 0.099Eab	0.921 ± 0.037Eb

A~E indicates a significant difference between OD value at different culture times (P < 0.05)

a~b indicates a significant difference between OD value at different proportion of macromolecules and small molecule peptides in MPH (P < 0.05)

Fig. 1

Effect of different proportion of macromolecules and small molecule peptides in MPH on viable counts after 24 h of incubation. In the figure, 1:1, 2:3, 3:7, 1:4, 1:9 refers to the ratio of macromolecules and small molecule peptides at MPH. a~d indicates a significant difference between viable counts at different proportion of macromolecules and small molecule peptides (P < 0.05)

During 0–16 h, the OD600 of the culture solution increased significantly and then became stable (i.e., no significant proliferation of Bifidobacterium L80) between 16 to 24 h. At 24 h, the OD600 of the culture treated with IFP containing MPH at a 1:9 of proteins and small molecule peptides was 1.079 ± 0.080. As shown (Fig. 1), the viable count at 24 h in MPH-enriched IFP comprising a 1:9 proportion of proteins and peptides (8.74 × 108 cfu/mL) was significantly greater than that in the blank group (5.94 × 108 cfu/mL) and that in the control group (6.85 × 108 cfu/mL) (P < 0.05). From the data in Table 1 and Fig. 1, it can be seen that the concentration of viable bacteria was related to the proportion of proteins and peptides in the MPH. MPH-enriched IFP with the protein to small molecule peptide ratio of 1:9 had the best proliferation on bifidobacterium L80. The OD600 of bifidobacterium L80 was the highest (indicating the greatest proliferative effect; equating to 1.54 times and 1.17 times the value for the blank group and the control group, respectively). The viable counts in the blank group were 1.47 times and 1.28 times as many as those in the control group, respectively, which were not considered significantly different.

Li et al. [25] used soybean protein and soybean peptides digested in vitro to prepare different nitrogen-containing media for the culture of Animal Bifidobacterium Subspecies. The results showed that soybean protein and soybean peptide could promote the growth and metabolism of Animal Bifidobacterium Subspecies. The effect of digesting soybean peptides was considered better. Bai et al. [4] analysed soybean protein (MW < 5000 Da) hydrolysates that’s rich in short peptides for the presence of 20 different full-valent amino acids in their complement of free amino acids. Although the amount of soybean protein hydrolysate added to the cultures contained only one third of the 20 amino acids, the maximum growth rate of these cultures was fivefold greater than that of the cultures treated with all 20 full-valent amino acids. The small molecular weight is not the whole reason for promoting the proliferation of probiotics. The results showed that the greatest growth-rate-enhancing hydrolysate was that with the richest nitrogen source that could be most easily used by lactic acid bacteria. These bacteria have low protease activity, so it is necessary to provide cultures with essential amino acids, vitamins and other growth factors, depending on the growth environment, to obtain high-density cell cultures.

Other researchers have emphasised the role of oligopeptides: Tynkkynen et al. [39] suggested that 98% of the nitrogen source for Lactococcus lactis growth relies on oligopeptides in milk, in which oligopeptide transport system plays a key role. Pritchard et al. [32] proved that the proliferation of lactic acid bacteria relies on dipeptides and tripeptides, in addition to six amino acids, to form oligopeptide systems. Although all of these systems involve the absorption of essential amino acids in nutrient media, the highest absorption rate is achieved by transporting dipeptides and tripeptides. Therefore, it’s reasonable to infer that proteolysis products with the highest content of short peptides (dipeptides and tripeptides) have the greatest growth-enhancing effects on the growth of Lactobacillus spp.

The role of lactoprotein also depends on the performance of Lactobacillus proteolytic enzymes and peptide transport systems, according to recent studies [7, 19, 44]. Lactobacillus growth in milk was found to depend on its protein hydrolysis system: casein was degraded by enzyme to form polypeptide fragments, oligopeptides are transported into cells by transporters, intracellular peptides was degraded into amino acids by enzyme. Kieliszek et al. [21] and Lazzi et al. [22] came to similar conclusions. Study of the proliferation experiments of lactic acid bacteria with functional feather proteins, showed that most of the soluble proteins of functional feather proteins are composed of smaller, soluble peptides. We need to further verify and analyse the various opinions about the reasons for the proliferation of probiotics promoted by lactin peptides.

The effect of MPH containing high levels of peptides on the titration acidity of Bifidobacterium L80 medium is shown in Table 2. The acidity of the culture fluids in each group increased rapidly over 0–16 h, which may be due to rapid proliferation generating a high concentration of acidic metabolites. Over the 16–24 h period, the increase in acidity was not significant, which could indicate that during this period of time, nutrients required by Bifidobacterium L80 (e.g., sugars) were almost exhausted, or the Bifidobacterium L80 culture was in decline. Overall: in the beginning, rapid bacterial growth during the logarithmic phase (as indicated by the steep OD600 curve during this period) increased the acidity of the system, and then short peptides generated by proteolysis promoted bacterial growth and thus increased the acid production capacity of Bifidobacterium L80. In Table 2 it shows that that acidity stabilised at approximately 16 h, indicating that Bifidobacterium L80 is at the end of its stable growth period. This slow growth can be attributed to the depletion of nutrient supplies, and the inhibition of growth by higher concentration of acidic metabolites.

Table 2

Effect of different proportion of macromolecules and small molecule peptides in MPH on titratable acidity during 24 h of incubation

Macromolecules/small molecule peptides	0 h	4 h	8 h	12 h	16 h	20 h	24 h
Blank	23.10 ± 1.09Aa	32.00 ± 1.09Aa	52.20 ± 0.95Ca	52.80 ± 1.09Ba	61.80 ± 1.19Ea	65.10 ± 1.78Ea	79.00 ± 2.44Ea
5:5	23.10 ± 2.14Aa	35.90 ± 1.09Aa	55.80 ± 2.53Ca	58.80 ± 1.09Ba	67.80 ± 1.32Ea	79.10 ± 2.36Ea	87.00 ± 2.66Ea
4:6	23.60 ± 3.13Aa	38.30 ± 1.09Aa	58.80 ± 1.61Cb	63.70 ± 1.09Ba	73.70 ± 2.23Eb	84.40 ± 2.06Ea	87.82 ± 1.63Eb
3:7	23.90 ± 2.37Aa	38.50 ± 1.09Aa	58.40 ± 3.05Cb	72.40 ± 1.09Ba	78.50 ± 2.06Eb	84.30 ± 2.06Ea	93.60 ± 1.76Eb
2:8	23.50 ± 3.99Aa	39.80 ± 1.09Aa	60.80 ± 2.91Cb	79.50 ± 1.09Ba	87.00 ± 1.75Eb	85.10 ± 1.85Ea	94.55 ± 2.35Eb
1:9	23.2 ± 2.47Aa	41.2 ± 1.09Aa	61.20 ± 2.76Cb	71.2 ± 1.09Ba	83.00 ± 2.95Eb	86.8 ± 2.06Ea	95.6 ± 6.26Eb
Control	23.70 ± 3.01Aa	38.50 ± 1.09Aa	51.20 ± 3.98Cb	58.00 ± 1.09Ba	63.70 ± 4.33Eb	68.60 ± 2.23Ea	71.90 ± 3.05Eb

A~E indicates a significant difference between the titratable acidity at different culture times (P < 0.05)

a~b indicates a significant difference between the titratable acidity at different TCA-NSI MPH (P < 0.05)

After incubation for 24 h, the titration acidity of the blank and control groups cultures increased to 79.0°T and 71.9°T, respectively, compared to an increase in cultures treated with MPH-enriched IFP of formula powder (containing a 90% proportion of proteins and small molecule peptides) of 95.6°T, which was significantly different (P < 0.05). From the growth and acidity change of Bifidobacterium L80, it can be observed that continuous production of acid also has a significant effect on the viability of Bifidobacterium L80; i.e. the concentration of bacteria decreased significantly after 24 h, indicating that the acid environment (lactic acid) is beneficial to probiotics, but only up to a certain point. Excessive acidity will have a bad effect on the activity of the bacteria, and the effect of acidity on viability is direct, and is consistent with the results reported by Dave and Shah et al. [10].

Inhibitory of Bifidobacterium L80 to E. coli BL21

Different proportions of proteins and small peptides of MPH showed different inhibitory effects on E. coli BL21, as shown in Fig. 2. It was observed that an increase in the proportion of proteins and small peptides in the MPH-enriched IFP led to an increase in the diameter of the inhibition zone of E. coli, showing that an increased proportion of proteins and small molecule peptides in MPH promotes the antibacterial action of Bifidobacterium L80 in the IFP. For example, when the MPH in the IFP comprised 90% proteins and small peptides, the inhibition zone diameter was 9.80 mm, which was 1.20 mm and 1.00 mm longer than in the blank group and the control group, respectively.

Fig. 2

Effect of different proportion of macromolecules and small molecule peptides in MPH on Bifidobacterium L80 and thus the effect of the metabolites on the inhibition of E. coli. In the figure, 1:1, 2:3, 3:7, 1:4, 1:9 refers to the ratio of macromolecules and small molecule peptides at MPH. a~b indicates a significant difference between the metabolites on the inhibition of E. coli. at different MPH addition (P < 0.05)

Some studies have suggested that the addition of polypeptides and amino acids to the culture medium is an effective way to increase the growth rate of lactic acid bacteria, and that whey protein hydrolysates have a positive effect on the formation of extracellular polysaccharides and the reduction of antigenicity [18, 48].

Casein hydrolysates also have a promoting effect on probiotic growth and show different degrees of inhibition of harmful bacteria. Zhi et al. [47] continuously fed cyclic guanosine monophosphate (CGMP), of mice to CGMP, and found that after 15 days, levels of Lactobacillus, Enterobacteriaceae and Bifidobacterium were significantly increased (P < 0.01), whilst levels of coliform bacteria were significantly reduced (P < 0.05).

Studies have shown that the protective effect of lactic acid bacteria on foods is mainly due to the production of some active metabolites, such as organic acids, which can inhibit the growth of spoilage and harmful microorganisms by lowering the pH of the system, as well as other substances such as ethanol, fatty acids, hydrogen peroxide, diacetyl, propionate, and phenyl lactic acid. Cyclic dipeptides and 3-hydroxy fatty acids, bacteriocins, and bacteriocins are also known playing a role in this protective effect [11, 37].

Metabolite analysis

Evaluation of the organic acid content

HPLC chromatograms of seven organic acids are shown in Fig. 3, and the linear equation for the determination of organic acids is shown in Table 3.

Fig. 3

HPLC analysis of organic acid. A HPLC analysis of organic acid standard samples. Peaks: (1) formic acid; (2) oxalic acid; (3) malic acid; (4) acetic acid; (5) tartaric acid; (6) lactic acid; (7) citric acid. B HPLC analysis of organic acid produced by Bifidobacterium L80 during 72 h in different medium. B: blank group; S: sample group; C:control group

Table 3

Linear correlation of organic acid determination

Peak number	Organic acid	Peak time(min)	Equation of linear regression	r2
1	Formic acid	2.403	y = 80640x + 3.210	0.981
2	Oxalic acid	2.745	y = 3543.7x + 14.869	0.988
3	Malic acid	2.957	y = 2199.22x + 0.9188	0.992
4	Acetic acid	3.594	y = 139.02x + 0.7112	0.996
5	Tartaric acid	3.957	y = 467.63x–1.565	0.973
6	Lactic acid	4.567	y = 1750.12x + 0.8043	0.999
7	Citric acid	6.309	y = 1884.03x-0.1525	0.987

The acid production of Bifidobacterium L80 is observed by titratable acidity assay, and HPLC can accurately quantitate the organic acids produced by metabolism. The results are shown in Table 4 and Fig. 3.

Table 4

Changes of organic acids content between blank group, sample group and control group

Group	0 h	12 h	24 h	36 h	48 h	60 h	72 h
Formic acid
S	375.23 ± 13.96Aa	346.60 ± 41.73Aa	363.71 ± 30.42Aa	316.24 ± 46.37Aa	296.80 ± 38.54Ac	368.52 ± 64.11Aa	323.46 ± 29.25Aa
C	132.55 ± 14.98Ab	136.46 ± 16.92Aa	148.86 ± 17.71Aa	171.44 ± 17.08Ba	172.66 ± 16.84Ba	180.43 ± 19.77Ba	170.89 ± 26.31Ba
B	161.66 ± 21.25Aa	169.25 ± 19.69Aa	162.05 ± 7.05Aa	175.36 ± 17.74Ba	179.44 ± 14.49Ba	176.04 ± 18.83Ba	182.36 ± 24.02Ba
Malic acid
S	1509.57 ± 13.26Aa	1796.97 ± 47.06Ba	1713.53 ± 38.01Ba	1746.78 ± 26.62Ba	1795.79 ± 26.36Ba	3509.39 ± 6.55Ca	3964.10 ± 32.18Ca
C	984.97 ± 51.64Ab	1545.00 ± 4.17Bb	8824.06 ± 40.23Cb	4276.99 ± 73.35Db	3798.85 ± 10.08Eb	829.83 ± 87.97Ab	816.47 ± 36.04Ab
B	740.72 ± 19.22Ac	884.60 ± 18.61Bc	875.05 ± 39.19Bc	1107.02 ± 70.78Cc	1121.89 ± 46.17Cc	1203.91 ± 27.87Cc	1211.81 ± 33.16Cc
Acetic acid
S	11,808.40 ± 37.46Aa	10,749.70 ± 71.55Aa	15,281.85 ± 36.09Ba	25,955.56 ± 24.28Ca	19,537.92 ± 46.78 Da	26,054.04 ± 46.61Ea	28,959.24 ± 53.51Fa
C	11,999.17 ± 48.58Aa	39,144.76 ± 54.20Bb	28,442.37 ± 72.75Cb	19,331.98 ± 30.87Db	37,808.13 ± 40.42Ea	13,416.85 ± 57.67Fb	14,136.17 ± 67.28Fb
B	11,979.74 ± 259.99Aa	11,712.70 ± 152.85Ba	22,185.18 ± 40.65Cc	26,274.13 ± 52.95Dc	26,223.01 ± 31.54Ec	23,345.78 ± 68.56Fc	20,390.12 ± 58.00Gc
Tartaric acid
S	7076.60 ± 45.05Aa	10,936.73 ± 175.16Ba	8280.10 ± 129.98Ca	14,642.50 ± 162.01 Da	15,503.45 ± 190.70Ca	22,189.72 ± 17.13 Da	8028.57 ± 250.80Ca
C	3021.09 ± 69.46Aa	4423.68 ± 287.38Bb	2279.29 ± 146.66Bb	3634.52 ± 63.66Bb	11,095.15 ± 76.35Bb	6527.85 ± 22.87Bb	10,804.73 ± 78.58Bb
B	8080.52 ± 664.09Aa	4796.85 ± 698.35Bb	26,237.91 ± 279.37Bc	29,573.06 ± 453.82Cc	5593.38 ± 48.66Dc	33,504.45 ± 34.46Ec	4656.49 ± 24.51Bc
Lactic acid
S	15,928.88 ± 38.46Aa	23,462.22 ± 98.99Ba	38,533.43 ± 31.55 Da	44,123.76 ± 216.39Ea	52,962.41 ± 64.50Fa	60,765.36 ± 73.53 Ga	683,687.47 ± 36.87Ha
C	19,988.31 ± 316.88Ab	13,108.94 ± 1240.51Bb	12,969.60 ± 257.78Cb	13,411.65 ± 1328.58Bb	12,128.05 ± 702.84Bb	11,317.57 ± 62.91Bb	11,190.02 ± 60.49Bb
B	13,539.66 ± 56.66Aa	14,016.28 ± 31.51Bc	14,262.22 ± 56.59Cc	48,697.84 ± 67.83Dc	59,608.36 ± 1291.34Dc	61,204.75 ± 1128.17 Da	63,937.61 ± 5136.01Dc
Citric acid
S	2833.59 ± 250.87Aa	1827.42 ± 142.72Aa	507.97 ± 50.07Aa	539.52 ± 43.98Aa	188.95 ± 77.93Aa	1955.97 ± 47.73Aa	478.22 ± 28.26Aa
C	1301.16 ± 83.21Ab	1791.26 ± 50.82Ba	822.82 ± 40.27Cb	635.84 ± 186.69Db	849.45 ± 20.53Cb	1406.05 ± 62.47Eb	1545.00 ± 46.72Eb
B	748.19 ± 39.63Ac	613.27 ± 163.18Ac	430.99 ± 79.94Bc	1227.71 ± 46.07Cc	2060.72 ± 57.59Dc	797.49 ± 48.12Ec	549.27 ± 105.85Fc

In the figure, S refers to the sample group with 1:9 proportion of macromolecules and small molecule peptides in MPH addition to MRS medium; C refers to the control group with the milk protein addition to MRS medium; B refers to the blank group with the basic MRS medium. A−H Different alphabets indicate significant differences between different time at the same group (P < 0.05). a−c Different alphabets indicate significant differences between sample groups, control group and bland group within a row (P < 0.05)

The data in Table 4 show that concentration of acetic acid and lactic acid were the highest in the metabolites of Bifidobacterium cultures treated with MPH-enriched IFP after 72 h fermentation, being 28959.24 ± 53.51 and 683687.47 ± 36.87 mg/L, respectively. Additionally, concentrations of formic acid, acetic acid, malic acid, and lactic acid were also significantly higher than those of the blank and the control at that time. These results show that MPH-enriched IFP promotes probiotics to proliferate and generates primarily acetic acid (C2 chain-length) and lactic acid (C3 chain length) as metabolites, and that these short-chain organic acids have a positive antibacterial effect. Indeed, Rios-Covian et al. [34] concluded that Acetic acid was the most abundant organic acid formed followed by lactic acid, with moderate differences in production among strains; pyruvic, succinic and formic acids were also produced at considerably lower proportions, with variability among strains.

Blandino et al. [3] have verified by in vitro experiments that Bifidobacteria can produce organic acids and inhibit Gram-negative pathogenic bacteria.

Evaluation of the hydrogen peroxide content

The viability of probiotics is affected by pH value and also by hydrogen peroxide and dissolved oxygen [10, 14, 42]. The results of measuring the hydrogen peroxide (H2O2) content in the metabolite profile of the Bifidobacterium L80 fermentation broth supplemented with MPH for 24 h are shown in Fig. 4.

Fig. 4

The content of H2O2 in the metabolites of Bifidobacterium L80 fermentation broth of with 1:9 proportion of macromolecules and small molecule peptides in MPH cultured for 24 h. In the figure, MPH refers to the sample group with 1:9 proportion of macromolecules and small molecule peptides in MPH addition to MRS medium; Control refers to the control group with the milk protein addition to MRS medium; Blank refers to the blank group with the basic MRS medium. a−b Different alphabets indicate significant differences between sample group, control group and blank group within a row (P < 0.05)

The concentration of H2O2 in the fermentation broth of the MPH group is 30.49 µg/mL, significantly higher than those in the blank group and control groups. Under these conditions, the death of bacterial cells can be ascribed to the accumulation of H2O2-mediated irreversible oxidative damage of cell membranes, proteins, enzymes and DNA [12, 13]. These observations indicate that certain concentrations of extracellular H2O2 may serve bacteriostatic functions in host-defence mechanisms. Thus, this study confirms and extends the observations of Hiromi Kameya et al. [16], which concluded that H2O2 has bacteriostatic effects on E. coli BL21.

Conclusions

All in all, MPH, as a supplement for IFP, has positive effect on the growth of Bifidobacterium L80. As the proportion of proteins to peptides in MPH increased, both cell density and viable counts of Bifidobacterium L80improved significantly. MPH also improved the inhibition of the growth of E. coli BL21 by producing organic acids and H2O2. With proper selection of MPH additions, IFP has potential to afford nutritional and health benefits to infant. This study expanded the application of MPH-enrich IFP in the field of Bifidobacterium, provided a reference to the production of infant formula to improve infant’s intestinal health.