Probiotic Potential of Lactiplantibacillus plantarum and its Fermented Foods: History
Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor: , , , , ,

Lb. plantarum is a kind of lactic acid bacteria (LAB) widely distributed in fermented food and the human intestinal tract, some strains of which have important effects on human health and the potential to be developed into probiotics.

  • Lactiplantibacillus plantarum
  • fermentation
  • probiotic functional foods

1. Probiotic Potential of Lb. plantarum and Foods Fermented with It

Lb. plantarum belongs to the genus Lactobacillus, which is widely considered to be a probiotic, and may have probiotic potential from species analysis. However, a prerequisite for probiotics to function in the host’s gastrointestinal tract is a good tolerance to unfavorable factors such as gastric acid, bile salts, and degrading enzymes, as well as the ability to complete colonization in the gastrointestinal tract [1]. Therefore, Lb. plantarum must have a high gastrointestinal survival rate to meet the basic requirements for development as a probiotic. Kriti Ghatani and Buddhiman Tamang [2] isolated a strain of Lb. plantarum from fermented yak milk products, and then added cholesterol and bile salts to MRS broth to determine the tolerance of the selected strain. Combined with acid resistance, bile salt hydrolase activity and cell surface hydrophobicity, they confirmed that this strain of Lb. plantarum was tolerant to the corrosive and toxic effects of gastric acid and bile in humans, and can adhere to host cells to complete colonization. Wang, G.Q. and Chen, Y. et al. [3] recorded the images of mouse intestines at different times after oral administration of Lb. plantarum, confirming that Lb. plantarum AR17-1 can colonize and play a role in the intestinal tract, implying that Lb. plantarum has probiotic potential.
As a carrier for Lb. plantarum to enter the human body, Lb. plantarum-fermented foods with high live counts have the potential to be developed into probiotic foods that can play a healthy role in the human body. However, the ability of these fermented foods to function as probiotic foods also depends on the gastrointestinal survival of the probiotic bacteria in the food. Different food matrices also have significant impacts on the gastrointestinal survival rate of Lb. plantarum. The most widely used matrices are dairy products including yogurt, cheese, etc. The higher fat and whey protein content in dairy products result in their better buffering capacity against gastric acid, which can improve the gastrointestinal survival rate of probiotics [4][5]. In addition, other fermented foods, such as fruit and vegetable juices, oats and cereals, and meat products are also commonly used as food matrices to create fermented foods that bring probiotics into the human gastrointestinal tract. The fat in meat products protects probiotics from low pH and bile salts [5], the higher sugar content in cereals allows probiotics to better tolerate intestinal conditions [6], and the relatively short digestion time of fruit and vegetable juices can greatly reduce the adverse effects of the gastric environment on probiotics [7][8]. Current Lb. plantarum-fermented foods that may have probiotic potential include dairy products, meat products, soy products, fruits and vegetables, and cereals, where the gastrointestinal survival of Lb. plantarum. is high. However, studies on the effect of food matrices on the gastrointestinal survival rate of probiotics are still relatively few, and it is hoped that more research will focus on this in the future.

2. Recent Developments in Lb. plantarum-Fermented Food

As mentioned above, Lb. plantarum has the potential to be developed as a probiotic because of its excellent anti-cardiovascular properties, as well as its good tolerance in the gastrointestinal tract, which is important for human health. In addition, some studies have demonstrated that foods fermented with it have better health benefits than before fermentation, and may have the ability to be developed into probiotic functional foods. The applications of Lb. plantarum in different types of foods, and the corresponding effects of its fermented foods, are shown in Figure 1 and Table 1.
Figure 1. The application of Lactiplantibacillus plantarum in several different types of food. Lactiplantibacillus plantarum has been widely used as a fermenting strain in the production of a wide range of fermented foods. (Created with Biorender.com).
Table 1. The effects of Lb. plantarum fermented foods in the prevention of different diseases.

2.1. Fermented Food with Antioxidant Function

Fruits and vegetables are rich in phenolic substances, carotenoids, flavonoids, and vitamin C, which have good antioxidant effects. Therefore, scientists hope to develop functional beverages based on fruit and vegetable juices and improve their antioxidant capacity through fermentation. In earlier research, some fermented juices with antioxidant functions, such as apple, orange, jujube, and coconut juices have been produced and proven to have a better ability to scavenge free radicals. In recent years, there have also been many reports on the antioxidant functional juice fermented by Lb. plantarum. Wu, Li, et al. [28] compared the antioxidant activity of blueberry and blackberry juices before and after fermentation based on ABTS methods, and they found that the ABTS radical scavenging activity of blackberry and blueberry juices fermented with Lactobacillus plantarum increased by 53.3% and 64.0%, respectively, compared to the juice before fermentation. The same results were also reported in fermented vegetable juice. Zhang, Duan, et al. [29] also found that the DPPH radical scavenging rate and ABTS free radical scavenging rate of carrot juice after 72 h of fermentation by Lb. plantarum WZ-01 were increased to some extent compared to their pre-fermentation state. These results suggest that fermentation by Lb. plantarum can effectively enhance the free radical scavenging activity of juices, and fermented fruit and vegetable juices can be developed as a good antioxidant functional beverage.
In addition to fruit and vegetable juice, there are also reports on the application of Lb. plantarum in the fermentation of other types of foods, including dairy products [17], soybean products [14], fermented sausages [24]. All these types of fermented foods show better antioxidant capacity in vitro compared with prior to fermentation.

2.2. Fermented Food with Cholesterol-Lowering Function

The development of Lb. plantarum-fermented foods with cholesterol-lowering effects have achieved some results, including dairy products, soybean products, fruits and vegetables, aquatic products. As early as 2015, Jeon, Lee, et al. [30] isolated a strain of lactic acid bacteria from kimchi that could lower cholesterol in vitro, named Lb. plantarum EM. Four years later, they utilized Lb. plantarum EM as a fermenting strain in cabbage-apple juice to investigate the health-promoting effects of fermented juice on high-cholesterol diet rats. It was found that the serum levels of TG, TC, and LDL-C were greatly reduced, and HDL-C levels were increased in rats fed with fermented juice compared to unfermented juice. Many scientists have obtained similar results with different types of fermented foods. Cao, Wu, et al. [16] pointed out that soy extract fermented by Lb. plantarum could regulate lipid metabolism through signaling pathways and thus lower cholesterol. Li, Wu, et al. [20] analyzed the microbial diversity of rat feces and found that skim milk fermented with Lb. plantarum WW could regulate intestinal flora and lower cholesterol levels. Hu, Zheng, et al. [13] found that Lb. plantarum FZU3013-fermented Laminaria japonica could affect the expression of genes involved in lipid metabolism and bile acid homeostasis in rats.

2.3. Fermented Food with Blood Pressure Lowering Function

There are few reports on the hypotensive effects of Lb. plantarum-fermented foods, and most of those reports focused on fermented foods that can inhibit ACE activity and are mainly fermented dairy products. In addition to dairy products, the same findings have been reported for other fermented foods, such as soy milk [31], fermented sausages [32], and fruits like guava [33]. However, due to the lack of relevant studies, it cannot be ascertained whether fermented foods are effective in in vivo experiments.

2.4. Fermented Food with Hypoglycemic Function

Several studies have confirmed the hypoglycemic effect of Lb. plantarum-fermented foods. Zhong, Abdullah, et al. [11] used blueberry as a fermentation substrate. Blueberries are widely considered to have a good antidiabetic ability and the potential to treat early-stage diabetes. In their research, they found that, compared with the non-fermented blueberry juice, the fumarate contents in blueberry juice fermented by Lb. plantarum were significantly increased, which could maintain glucose homeostasis. In addition, fermentation altered the concentrations of phenolic compounds in blueberry juice, which promoted glucose consumption. They employed HepG2 cell lines as a model to confirm that fermented juice significantly enhanced cellular glucose consumption [34]. In addition to this, Lb. plantarum fermentation also increases α-Amylase and α-glucosidase inhibitory activity, thus reducing carbohydrate hydrolysis for the effective control of diabetes [35].

2.5. Other Applications of Lb. plantarum

In conclusion, it can be seen that Lb. plantarum-fermented foods show good effects in in vitro experiments, and have the potential to be developed into probiotic products. Moreover, in addition to conferring additional functional characteristics to the foods, Lb. plantarum fermentation may improve the properties of traditional fermented foods. Compared with unfermented food, fermented food can produce bacteriocins with good antimicrobial properties and extended storage time [36]; it may also have better stability [37], and its flavor will be improved to meet consumers’ demands [9]. At present, there are various kinds of functional fermented foods reported covering the basic diet, such as dairy products, fruits, vegetables, meat products, soybeans, and cereals. These factors comprehensively show that developing Lb. plantarum-fermented foods and supplementing these foods in daily life may be of great significance to human health.

This entry is adapted from the peer-reviewed paper 10.3390/foods11172549

References

  1. Han, S.; Lu, Y.; Xie, J.; Fei, Y.; Zheng, G.; Wang, Z.; Liu, J.; Lv, L.; Ling, Z.; Berglund, B.; et al. Probiotic Gastrointestinal Transit and Colonization After Oral Administration: A Long Journey. Front. Cell. Infect. Microbiol. 2021, 11, 609722.
  2. Ghatani, K.; Tamang, B. Assessment of probiotic characteristics of lactic acid bacteria isolated from fermented yak milk products of Sikkim, India: Chhurpi, Shyow, and Khachu. Food Biotechnol. 2017, 31, 210–232.
  3. Wang, G.; Chen, Y.; Fei, S.; Xie, C.; Xia, Y.; Ai, L. Colonisation with endogenous Lactobacillus reuteri R28 and exogenous Lactobacillus plantarum AR17-1 and the effects on intestinal inflammation in mice. Food Funct. 2021, 12, 2481–2488.
  4. Galdino, I.K.C.P.D.O.; Oliveira, M.M.; Oliveira, A.T.; da Silva, G.M.; de Oliveira, T.A.; dos Santos, K.M.O.; Egito, A.S.D.; Buriti, F.C.A. Fermentative behavior of native lactobacilli in goat milk and their survival under in vitro simulated gastrointestinal conditions. LWT 2020, 135, 109905.
  5. Flach, J.; van der Waal, M.; Nieuwboer, M.V.D.; Claassen, H.; Larsen, O.F.A. The underexposed role of food matrices in probiotic products: Reviewing the relationship between carrier matrices and product parameters. Crit. Rev. Food Sci. Nutr. 2017, 58, 2570–2584.
  6. Sharma, R.; Mokhtari, S.; Jafari, S.M.; Sharma, S. Barley-based probiotic food mixture: Health effects and future prospects. Crit. Rev. Food Sci. Nutr. 2021, 1–15.
  7. Zhu, W.; Lyu, F.; Naumovski, N.; Ajlouni, S.; Ranadheera, C.S. Functional Efficacy of Probiotic Lactobacillus sanfranciscensis in Apple, Orange and Tomato Juices with Special Reference to Storage Stability and In Vitro Gastrointestinal Survival. Beverages 2020, 6, 13.
  8. De Oliveira, P.M.; de Castro Leite Junior, B.R.; Martins, E.M.F.; Martins, M.L.; Vieira, N.R.; de Barros, F.A.R.; Cristianini, M.; de Almeida Costa, N.; Ramos, A.M. Mango and carrot mixed juice: A new matrix for the vehicle of probiotic lactobacilli. J. Food Sci. Technol. 2020, 58, 98–109.
  9. Gao, H.; Wen, J.-J.; Hu, J.-L.; Nie, Q.-X.; Chen, H.-H.; Nie, S.-P.; Xiong, T.; Xie, M.-Y. Momordica charantia juice with Lactobacillus plantarum fermentation: Chemical composition, antioxidant properties and aroma profile. Food Biosci. 2019, 29, 62–72.
  10. Chen, R.; Chen, W.; Chen, H.; Zhang, G.; Chen, W. Comparative Evaluation of the Antioxidant Capacities, Organic Acids, and Volatiles of Papaya Juices Fermented by Lactobacillus acidophilus and Lactobacillus plantarum. J. Food Qual. 2018, 2018, 1–12.
  11. Zhong, H.; Abdullah; Zhao, M.; Tang, J.; Deng, L.; Feng, F. Probiotics-fermented blueberry juices as potential antidiabetic product: Antioxidant, antimicrobial and antidiabetic potentials. J. Sci. Food Agric. 2021, 101, 4420–4427.
  12. Shikano, A.; Kuda, T.; Shibayama, J.; Toyama, A.; Ishida, Y.; Takahashi, H.; Kimura, B. Effects of Lactobacillus plantarum Uruma-SU4 fermented green loofah on plasma lipid levels and gut microbiome of high-fat diet fed mice. Food Res. Int. 2019, 121, 817–824.
  13. Hu, J.-P.; Zheng, T.-T.; Zeng, B.-F.; Wu, M.-L.; Shi, R.; Zhang, Y.; Chen, L.-J.; Cheng, W.-J.; Liang, P. Effects of Lactobacillus plantarum FZU3013-Fermented Laminaria japonica on Lipid Metabolism and Gut Microbiota in Hyperlipidaemic Rats. Front. Nutr. 2021, 8, 786571.
  14. Tsui, C.-Y.; Yang, C.-Y. Evaluation of Semi-Solid-State Fermentation of Elaeocarpus serratus L. Leaves and Black Soymilk by Lactobacillus plantarum on Bioactive Compounds and Antioxidant Capacity. Foods 2021, 10, 704.
  15. Mirlohi, M.; Babashahi, M.; Ghiasvand, R.; Azadbakht, L.; Mosharaf, L.; Torki-Baghbadorani, S. Effects of probiotic soy milk fermented by lactobacillus plantarum A7 (KC 355240) added with Cuminum Cyminum essential oil on fasting blood glucose levels, serum lipid profile and body weight in diabetic Wistar rats. Int. J. Prev. Med. 2020, 11, 8.
  16. Cao, C.; Wu, R.; Zhu, X.; Li, Y.; Li, M.; An, F.; Wu, J. Ameliorative effect of Lactobacillus plantarum WW-fermented soy extract on rat fatty liver via the PPAR signaling pathway. J. Funct. Foods 2019, 60, 103439.
  17. de la Fuente, B.; Luz, C.; Puchol, C.; Meca, G.; Barba, F.J. Evaluation of fermentation assisted by Lactobacillus brevis POM, and Lactobacillus plantarum (TR-7, TR-71, TR-14) on antioxidant compounds and organic acids of an orange juice-milk based beverage. Food Chem. 2020, 343, 128414.
  18. Mushtaq, M.; Gani, A.; Masoodi, F. Himalayan cheese (Kalari/Kradi) fermented with different probiotic strains: In vitro investigation of nutraceutical properties. LWT 2019, 104, 53–60.
  19. Moreno-Montoro, M.; Olalla-Herrera, M.; Rufián-Henares, J.; Martínez, R.G.; Miralles, B.; Bergillos, T.; Navarro-Alarcón, M.; Jauregi, P. Antioxidant, ACE-inhibitory and antimicrobial activity of fermented goat milk: Activity and physicochemical property relationship of the peptide components. Food Funct. 2017, 8, 2783–2791.
  20. Li, Y.; Wu, J.; Cao, C.; Zhu, X.; Sun, X.; Wu, R. Effects of skim milk fermented with Lactobacillus plantarum WW on the constitutions of rats fed a high-fat diet. J. Dairy Sci. 2020, 103, 5019–5029.
  21. Albano, C.; Morandi, S.; Silvetti, T.; Casiraghi, M.; Manini, F.; Brasca, M. Lactic acid bacteria with cholesterol-lowering properties for dairy applications: In vitro and in situ activity. J. Dairy Sci. 2018, 101, 10807–10818.
  22. Wang, M.; Lei, M.; Samina, N.; Chen, L.; Liu, C.; Yin, T.; Yan, X.; Wu, C.; He, H.; Yi, C. Impact of Lactobacillus plantarum 423 fermentation on the antioxidant activity and flavor properties of rice bran and wheat bran. Food Chem. 2020, 330, 127156.
  23. Wu, H.; Rui, X.; Li, W.; Xiao, Y.; Zhou, J.; Dong, M. Whole-grain oats (Avena sativa L.) as a carrier of lactic acid bacteria and a supplement rich in angiotensin I-converting enzyme inhibitory peptides through solid-state fermentation. Food Funct. 2018, 9, 2270–2281.
  24. Luan, X.; Feng, M.; Sun, J. Effect of Lactobacillus plantarum on antioxidant activity in fermented sausage. Food Res. Int. 2021, 144, 110351.
  25. Hashemi, S.; Raeisi, S.; Zanardi, E.; Paciulli, M.; Chiavaro, E. Antimicrobial and Antioxidant Activities of Fermented Meat Patty with Lactobacillus Strains. Ital. J. Food Sci. 2018, 30, 268–279.
  26. Ayyash, M.; Liu, S.-Q.; Al Mheiri, A.; Aldhaheri, M.; Raeisi, B.; Al-Nabulsi, A.; Osaili, T.; Olaimat, A. In vitro investigation of health-promoting benefits of fermented camel sausage by novel probiotic Lactobacillus plantarum: A comparative study with beef sausages. LWT 2018, 99, 346–354.
  27. Kong, Y.-W.; Feng, M.-Q.; Sun, J. Effects of Lactobacillus plantarum CD101 and Staphylococcus simulans NJ201 on proteolytic changes and bioactivities (antioxidant and antihypertensive activities) in fermented pork sausage. LWT 2020, 133, 109985.
  28. Wu, Y.; Li, S.; Tao, Y.; Li, D.; Han, Y.; Show, P.L.; Wen, G.; Zhou, J. Fermentation of blueberry and blackberry juices using Lactobacillus plantarum, Streptococcus thermophilus and Bifidobacterium bifidum: Growth of probiotics, metabolism of phenolics, antioxidant capacity in vitro and sensory evaluation. Food Chem. 2021, 348, 129083.
  29. Zhang, X.; Duan, W.; Zou, J.; Zhou, H.; Liu, C.; Yang, H. Flavor and antioxidant activity improvement of carrot juice by fermentation with Lactobacillus plantarum WZ-01. J. Food Meas. Charact. 2019, 13, 3366–3375.
  30. Bin Jeon, Y.; Lee, J.; Chang, H.C. Characterization of juice fermented with Lactobacillus plantarum EM and its cholesterol-lowering effects on rats fed a high-fat and high-cholesterol diet. Food Sci. Nutr. 2019, 7, 3622–3634.
  31. Singh, B.P.; Vij, S. Growth and bioactive peptides production potential of Lactobacillus plantarum strain C2 in soy milk: A LC-MS/MS based revelation for peptides biofunctionality. LWT 2017, 86, 293–301.
  32. Huang, L.; Feng, M.; Sun, J. Angiotensin-converting enzyme (ACE) inhibitory peptides from fermented sausages inoculated with Lactobacillus plantarum CD101 and Staphylococcus simulans NJ201. Int. J. Food Sci. Technol. 2022, 57, 4985–4997.
  33. de Oliveira, S.D.; Araújo, C.M.; Borges, G.D.S.C.; Lima, M.D.S.; Viera, V.B.; Garcia, E.F.; de Souza, E.L.; de Oliveira, M.E.G. Improvement in physicochemical characteristics, bioactive compounds and antioxidant activity of acerola (Malpighia emarginata D.C.) and guava (Psidium guajava L.) fruit by-products fermented with potentially probiotic lactobacilli. LWT 2020, 134, 110200.
  34. Zhang, Z.-P.; Ma, J.; He, Y.-Y.; Lu, J.; Ren, D.-F. Antioxidant and hypoglycemic effects of Diospyros lotus fruit fermented with Microbacterium flavum and Lactobacillus plantarum. J. Biosci. Bioeng. 2018, 125, 682–687.
  35. Ayyash, M.; Olaimat, A.; Al-Nabulsi, A.; Liu, S.-Q. Bioactive Properties of Novel Probiotic Lactococcus lactis Fermented Camel Sausages: Cytotoxicity, Angiotensin Converting Enzyme Inhibition, Antioxidant Capacity, and Antidiabetic Activity. Korean J. Food Sci. Anim. Resour. 2020, 40, 155–171.
  36. Hashemi, S.M.B.; Gholamhosseinpour, A. Fermentation of table cream by Lactobacillus plantarum strains: Effect on fungal growth, aflatoxin M1 and ochratoxin A. Int. J. Food Sci. Technol. 2018, 54, 347–353.
  37. Dan, T.; Chen, H.; Li, T.; Tian, J.; Ren, W.; Zhang, H.; Sun, T. Influence of Lactobacillus plantarum P-8 on Fermented Milk Flavor and Storage Stability. Front. Microbiol. 2019, 9, 3133.
More
This entry is offline, you can click here to edit this entry!
ScholarVision Creations