Lactic Acid Bacteria Project

LACTIC ACID BACTERIA

NAME : T.L.V.PEIRIS DEPARTMENT:FOOD SCIENCE UNIVERSITY: UNIVERSITY OF SRI JAYAWARDENAPURA YEAR : AUGUST 2009 STUDENT NUMBER: GS/MSc/Food/3630/08

Summery

Lactic acid bacteria in food are considered as GRAS. This report contents various aspects of  lactic acid bacteria. This report gives where these microorganisms thrive and their physiological characteristics. It further explains in very descriptive manner the major metabolic pathways which they use to metabolize sugar. Homofermentive metabolic pathway, Heterofermentative metabolic pathway (pentose phosphate pathway) and EMP pathways are given in detail. Furthermore this report gives the usage of Lactic acid bacteria in food and furthermore importance of Lactic acid bacteria as probiotics also briefly explained.

Key words: Lactic acid , Heterofermentative pathway, Homofermetative Homofermetative Pathway, EMP  pathway, probiotics

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Contents

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Introduction

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Characteristics

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Bio chemistry of Lactic acid bacteria

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metabolism of sugars

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Homferment entive metaboli olism of of he hexose ose

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Hete Hetero rofe ferm rmen enta tati tive ve meta metabo boli lism sm of hexo hexose sess

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Metabolism of malic acid

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Embd Embden en-M -Mey eyer erho hofff-Par -Parna nass pat pathway hway (EMP EMP) i. Activation of Glucose ii. Hexose Splitting iii Energy Extraction iv. End Product Formation

Lactic acid bacteria - their uses in food

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Probiotics and LAB

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Reference

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Introduction

The Lactic Acid Bacteria (LAB) comprise a clade of Gram-positive of Gram-positive,, low-G low-GC, acid-tolerant, generally non-sporulating, non-respiring rod or cocci that are associated by their common metabolic and physiological and physiological characteristics. These bacteria These bacteria,, usually found in decomposing plants and lactic products, produce lactic acid as the major metabolic end-product of carbohydrate of carbohydrate fermentation. This trait has, throughout history, linked LAB with food fermentations, fermentations, as acidification inhibits the growth of spoilage agents. Proteinaceous bacteriocins Proteinaceous bacteriocins are produced by several LAB strains and provide an additional hurdle for spoilage and pathogenic and pathogenic microorganisms. Furthermore, lactic acid and other metabolic products contribute to the organoleptic and textural profile of a food item. The industrial importance of the LAB is further  evidenced by their reputed safe (GRAS (GRAS)) status, due to their ubiquitous appearance in food and their contribution to the healthy microflora of human mucosal surfaces. The genera that comprise the LAB are at its core core Lactobacillus  Lactobacillus,, Leuconostoc  Leuconostoc,, Pediococcus  Pediococcus,, Lactococcus  Lactococcus,, and Streptococcus as well as the more peripheral Aerococcus Carnobacterium, Enterococcus  Enterococcus,, peripheral Aerococcus,, Carnobacterium, Oenococcus,, Sporolactobacillus Oenococcus Sporolactobacillus,, Teragenococcus, Teragenococcus, Vagococcus, Vagococcus, and Weisella; Weisella; these belong to the order Lactobacillales order Lactobacillales.. Characteristics

The Lactic Acid Bacteria (LAB) are rod-shaped bacilli rod-shaped bacilli or coccus or coccus.. LAB are characterized by an increased tolerance to a lower  pH  pH range. This aspect partially enables LAB to outcompete other   bacteria in a natural fermentation fermentation,, as they can withstand the increased acidity from organic acid  production (e.g., lactic acid). acid). Laboratory media used for LAB typically includes a carbohydrate source as most species are incapable of respiration. LAB are catalase negative. There are two main hexose fermentation pathways fermentation pathways that are used to classify LAB genera. Under  conditions of excess glucose and limited oxygen, homolactic LAB catabolize one mole of  glucose in the Embden-Meyerhof-Parnas (EMP) pathway to yield two moles of  pyruvate.  pyruvate. Intracellular redox Intracellular redox balance is maintained through the oxidation of  NADH,  NADH, concomitant with  pyruvate reduction to lactic acid. This process yields two moles ATP per glucose consumed. Representative homolactic LAB genera include Lactococcus include Lactococcus,, Enterococcus,  Enterococcus, Streptococcus, Streptococcus,  Pediococcus,  Pediococcus, and group I lactobacilli. Heterofermentative LAB use the pentose the pentose phosphate pathway, pathway, alternatively referred to as the  pentose phosphoketolase pathway. One mole Glucose-6-phosphate is initially dehydrogenated to 6-phosphogluconate and subsequently decarboxylated to yield one mole of CO2. The resulting  pentose-5-phosphate is cleaved into one mole glyceraldehyde phosphate (GAP) and one mole acetyl phosphate. GAP is further metabolized to lactate as in homofermentation, with the acetyl  phosphate reduced to ethanol via acetyl-CoA and acetaldehyde intermediates. In theory, end products (including ATP) are produced in equimolar quantities from the catabolism of one mole Oenococcus, Weissella, Weissella, and of glucose. Obligate heterofermentative LAB include Leuconostoc include Leuconostoc,, Oenococcus, group III lactobacilli.

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Lactic acid bacteria

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Metabolism of lactic acid bacteria Metabolism of Sugars

Lactic acid bacteria are chemotrophic, they find the energy required for their entire metabolism from the oxidation of chemical compounds. The oxidation of sugars constitutes the principle energy producing pathway. Lactic acid bacteria of the genera Lactobacillus, genera Lactobacillus, Leuconostoc and Pediococcus and Pediococcus,, the important  bacteria to winemaking, assimilate sugars by either a homofermentative or heterofermentative  pathway. Homofermentative Metabolism of Hexoses Homofermentative bacteria transform nearly all of the sugars they use, especially glucose into lactic acid. The homofermentative pathway includes a first phase of all the reactions of  glycolysis that lead from hexose to pyruvate. The terminal electron acc eptor in this pathway is  pyruvate which is reduced to lactic acid. See Figure 1. In fermentation, pyruvate is decarboxylated to ethanal, which is the terminal electron acceptor, being reduced to ethanol. Heterofermentative Metabolism of Hexoses Bacteria using the heterofermentative pathway, which includes Leuconostoc includes Leuconostoc (the most important  bacterium in enology) use the pentose phosphate pathway. In this pathway, NADPH is generated as glucose is oxidized to ribose 5-phosphate. This five-carbon sugar and its derivatives are components of important biomolecules such as ATP, CoA, NAD+, FAD, RNA and DNA. NADPH is the currency of readily available reducing p ower in cells (NADH is used in the respiratory chain). This pathway occurs in the cytosol.

After being transported into the cell, a glucokinase phosphorylates the glucose into glucose 6-P (glucose 6-phosphate). Its destination is completely different from the glucose 6-P in the homofermentative pathway. Two oxidation reactions occur: the first leads to gluconate 6-P and the second, accompanied by a decarboxylation, forms ribulose 5-P. See Figure 2. In each of these reactions a molecule of NADP+ is reduced. Ribulose 5-P can then be epimerized either  to ribose 5-P or to xylulose5-P. Xylulose 5-P is then cleaved into acetyl-phosphate and glyceraldehydes 3-phosphate. See Figure 3. The glyceraldehyde 3-phosphate is metabolized into lactic acid by following the same  pathway as in the homofermentative pathway. The acetylphosphate has two possible destinations, depending on environmental conditions. This molecule can be successively reduced into ethanal and ethanol, in which case the molecules of the coenzyme NADPH formed during the two oxidation reactions of glucose at the beginning of the heterofermentative pathway, are reoxidized. This reoxidation is essential for regenerating the coenzymes necessary for this pathway. The final products are then lactate and ethanol. Or the acetyl-phosphate can produce acetate (acetic acid) through the enzyme acetate kinase. This reaction also yields a molecule of ATP. The final products of this pathway are then lactate and acetate. Bacteria of the genus Leuconostoc genus Leuconostoc preferentially  preferentially produce lactate and ethanol in a slightly aerated environment and lactate and acetate in an aerated environment.

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Metabolism of Malic Acid The majority of bacterial species preponderant in wine after alcoholic fermentation break down malic acid. The most important bacterium in enology is the heterofermentative bacteria, Leuconostoc bacteria, Leuconostoc oenos. oenos. This bacterium forms Dlactic acid from glucose and L-lactic acid from L-malic acid.

The major distinction between wine and vinegar is the amount of acetic acid. The amount of  acetic acid is estimated from the volatile acidity or VA (the wine is steam distilled and the distillate titrated with sodium hydroxide using phenolphalein). A small amount of acetic acid is  produced by yeasts, in particular Saccharomyces particular Saccharomyces cerevisiae to the extent of 100-300 mg.L-1 (see Figure 5, Yeast Biochemistry, Sugars). Bacteria degrade must and wine sugars with a different affinity depending on the species. In general, bacterial development occurs after yeast dev elopment. Since the yeast has consumed the sugars, the lactic acid formed from them is small compared to the amount produced from malic acid.  L. oenos can and does produce acetic acid from glucose (see figures 3 & 4), but since the lactic acid formed from them is low, so is the acetic acid. An increase in the VA (acetic acid) of a wine coupled with an abnormal amount of lactic acid (>300 mg.L-1) indicates lactic disease and suggests the L. the L. oenos fermented a significant quantity of sugars.

Glycolysis - Embden-Meyerhoff-Parnas pathway (EMP)

EMP is the most commonly used series of reactions for oxidizing glucose to pyruvate and many  bacteria, animals and plants employ this pathway in their catabolism. EMP is so ubiquitous that is worthwhile to use it as an example of a typical fermentation. It is an essential part of many organisms catabolism, even yours! However, it is not the only method for the fermentation of  glucose. Remember that bacteria are remarkably creative and other pathways are present in different species. EMP can be divided into 3 stages, activation of glucose , hexose splitting and energy extraction

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Activation of Glucose

Glucose is a relatively stable molecule and in order to degrade it, it must first be destabilized by adding high energy phosphates. In the first step a phosphate is donated from ATP (or   phosphoenolpyruvate - the source of the phosphate depends on the species of microbe you look  at) to glucose to form glucose-6-phosphate. The molecule is isomerized to fructose-6-phosphate (another sugar) and a second phosphate is added. Fructose-1,6-bisphosphate is easier to attack  than glucose and is ready to be split.

Figure 3 - Activation of glucose by phosphorylation ph osphorylation with ATP. Hexose Splitting

Fructose bisphosphate aldolase then breaks the phosphate loaded fructose into two 3 carbon compounds, glyceraldehyde-3-phosphate (GAP) and dihydroxyacetonephosphate (DAP). This is the crucial step in the EMP pathway, converting the 6 carbon glucose molecule to two 3 carbon molecules that will eventually become pyruvate.

Figure 4 - Splitting of Fructose by aldolase. Energy Extraction

In the next reaction, DAP is converted into GAP, which can be acted on by the rest of the EMP. The next step is a very important one. Inorganic phosphate is added to GAP to make 1,3 bisphosphoglycerate (BPG). No energy is required and in fact electrons are transferred from GAP to NAD+. This reaction is the payback for running the pathway and the phosphates added here are later transferred to ADP to make ATP. After several enzymatic rearrangements, the final  product of the EMP pathway is pyruvate.

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Figure 5 - Extraction of Energy. Note the two reactions highlighted in blue that yield energy. Remember that each glucose molecule that comes into glycolysis generates two GAP molecules that can then proceed down the latter half of the pathway. The total reaction can be summarized as follows 2 ATP + glucose + 4 ADP + 2 Pi + 2 NAD+  NADH

2 ADP + 2 pyruvate + 4 ATP + 2

The blue highlight denotes energy put into the reaction. Subtracting this from the energy extracted, the net energy gain is 2 ATP per glucose. That is a lot of work for just 2 ATP. Fermentations do not yield large amounts of energy and this explains why fermenting microbes go through so much substrate without much growth. Some of the NADH that is generated can be used for cell biosynthesis, b iosynthesis, but there is a large excess or reducing power. Fermenting bacteria must find a way to get rid of these extra electrons and a nd they do it by adding them to pyruvate to form end products. End Product Formation

One of the more familiar fermentations is conversion of glucose to ethanol to form alcoholic  beverages. After the formation of pyruvate, ethanol is formed by two simple reactions. First, CO2 is removed from pyruvate to form acetaldehyde. Then acetaldehyde is reduced by, you guess it,  NADH

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Figure 6 - Oxidation of NADH. Acetaldehyde is reduced to ethanol (the active ingredient in alcoholic beverages). This is the final step in yeast fermentation of glucose to ethanol. Another favorite microbial fermentation is the formation of lactic acid. This is performed by the lactic acid bacteria. Homofermentative lactic acid bacteria use the EMP pathway to make  pyruvate and then reduce it to lactate using up their excess NADH in the process. Other bacteria use alternative pathways to generate lactate from glucose. Close examination of the heterofermentative pathway reveals that it does not use EMP at all. The take home message is, EMP is common, but there are many other ways of doing business. figure 7 - Formation of lactate by homofermentative bacteria. The pathway used is identical to glycolysis. The final end product is lactate which is excreted by the cells into their environment.

Figure 8 - Fermentation of glucose by heterofermentative bacteria. In this pathway the top part of  the glycolytic pathway is not used. Note the recycling of NADH and the low yield. Only one ATP is generated per glucose fermented.

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Lactic acid bacteria - their uses in food

Lactic acid bacteria have been used to ferment or culture foods for at least 4000 years. They are used in particular in fermented milk products from all over the world, including yoghurt, cheese,  butter, buttermilk, kefir and koumiss. Although they are best known for their role in the preparation of fermented dairy products, they are also used for pickling of vegetables, baking, winemaking, curing fish, meats and sausages. Witho Without ut unders understan tandin ding g the scient scientif ific ic basis, basis, people people thousa thousands nds of years years ago used used lacti lacticc acid acid  bacteria to produce cultured foods with improved preservation properties and with characteristic flavours and textures different from the original food. Similarly today, a wide variety of fermented milk products including liquid drinks such as kefir  and semi-solid or firm products like yoghurt and cheese respectively, make good use of these illustrious microbial allies. The manufacture involves a microbial process by which the milk sugar, lactose is converted to lactic acid. As the acid accumulates, the structure of the milk protein changes (curdling) and thus the texture of the product. Other variables such as temperature and the composition of the milk, also contribute to the particular features of different products. Lactic acid also gives fermented milks their slightly tart taste. Additional characteristic flavours and and arom aromas as are are ofte often n the the resu result lt of othe otherr prod produc ucts ts of lact lactic ic acid acid bacte bacteri ria. a. For For examp example le acetaldehyde, provides the characteristic aroma of yoghurt, while diacetyl imparts a buttery taste to other fermented milks. Additional micro-organisms such as yeasts can also be included in the culture to provide unique tastes. For example, alcohol and carbon dioxide produced by yeasts contri contribut butee to the refres refreshin hing, g, frothy frothy taste taste of kefir kefir,, koumiss koumiss and leben. leben. Other Other manufa manufactu cturin ring g techniques such as removing the whey or adding flavours, also contribute to the large variety of  available products. For yoghur yoghurt, t, the manufa manufactu cture re depends depends on a symbi symbioti oticc relati relations onship hip between between two bacter bacteria, ia, Streptococcus Streptococcus thermophilus thermophilus and  Lactobacil  Lactobacillus lus bulgaricus, bulgaricus, where where each each specie speciess of bacteri bacterium um stimulates the growth of the other. This interaction results in a shortened fermentation time and a  product with different characteristics than one fermented with a single species. With yoghurt and other fermented milks there are considerable opportunities for exploiting lactic acid acid bacter bacteria ia as probio probioti ticc cultur cultures. es. These These supple supplemen mentt and help help our normal normal gut bacter bacteria ia to function more efficiently. The world-wide market for these products continues to increase in response to the demands of an increasingly health-conscious public. Lactic acid bacteria are therefore excellent ambassadors for an often maligned microbial world. They are not only of major economic significance, but are also of value in maintaining and  promoting human health.

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Probiotics and LAB

Probiotics are products aimed at delivering living, potentially beneficial, bacterial cells to the gut ecosystem of humans and other animals, whereas prebiotics whereas prebiotics are non-digestible carbohydrates delivered in food to the large bowel to provide fermentable substrates for selected bacteria. Strains of LAB are the most common microbes employed a s probiotics. Two principal kinds of   probiotic bacteria, members of the genera Lactobacillus genera Lactobacillus and Bifidobacterium and Bifidobacterium,, have been studied in detail. Most probiotic strains belong to the genus Lactobacillus genus Lactobacillus.. Probiotics have been evaluated in research studies in animals and humans with respect to antibiotic-associated diarrhoea, travellers' diarrhoea, pediatric diarrhoea, inflammatory bowel disease, disease, and irritable bowel syndrome. syndrome. It is  possible that, in the future, probiotics will be used for different gastrointestinal diseases, vaginosis,, or as delivery systems for vaccines, immunoglobulins, and other therapies. vaginosis References 1. Collins, M. D., J. A. E. Farrow, B. A. Phillips, S.Ferusu, D. Jones.,1987. Int. J. Syst.  bacteriol.,37, 310 - 316. 2. Cone, D.K., 1982. J. Fish. Diseases, 5, 479-485. 3. De Man., J. C. Rogosa, M. E. Sharpe, 1960. J. Appl. Bacteriol., 23, 130-135. 4. Fricourt, B. V., S. F. Barefoot, R. F. Jestin, S. S. Hayasaka, 1994. J. Food. Prot., 57, 698 - 702. 5. Gancel, F., F. Dzierszinski, R. Tailliez, 1997.J. Appl. Microbiol., 82, 722-728. 6. Gonzalez, C. J., J. P. Encinas, M. L. Gracia-Lopez,A. Otero, 2000. Food. Microbiol., 17,383391. 7. Kandler, O., N. Weiss, 1986. In: Bergey'sManual of Systematic Bacteriology, P. H. A.Sneath,  N. S. Mair, M. E. Sharpe, J. G. Holt(Eds), Vol. 2, Baltimore: Williams and Wilkins,1209 – 1234. 8. Magnusson, H., K. Traudottir, 1982. J. Food.Technol., 17, 695-702. 9. Maugin, S., G. Novel, 1994. J. Appl. Bacteriol.,76, 616-625. 10. Molin, G., S. Inga-Maj, A. Ternstrom, 1983.J. Appl. Bacteriol., 55, 49-56. 11. Oberlender, V., M. O. Hanna, R. Miget, C. Vanderzant, G. Finne, 1983. J. Food. Prot., 46, 434-440. 12. Okafor, N., B. C. Nzeako, 1985. Food. Microbiol.,2, 71-75. 13. Ringoe, E., F. J. Gatesoupe, 1998. Aquaculture,160, 177 - 203. 14. Salminen, S., A. von Wright (Eds), 1998 . Lactic acid Bacteria Microbiology and Functional Aspects,2nd edn, NewYork: Marcel Dekker Inc, 180-193. 15. Sarkar, P. K., S. Banerjee, 1996. J. Food. Sci.Technol., 33, 231-233. 16. Schleifer, K. H., 1987. FEMS. Microbiol. Rev.,46, 201-203. 17. Schroder, K., E. Clausen, A. M. Sandberg,J. Raa, 1979. In: Advances in Fish Science and Technology, J. J. Connel (Ed.), Farnham, England: Fishing Newsbook Ltd, 480-483. 18. Sharpe, M. E., T. F. Fryer, D. G. Smith, 1979.Identification of Lactic Acid Bacteria. In: Identification Methods for Microbiologists, E. M.Gibbs, F. A. Skinner (Eds), London: Academic Press, 233-259. 19. Stiles, M. E., W. H. Holzapfel, 1997. 1 997. Int. J. Food.Microbiol., 36, 1-29. 20. Valdimarsson, G., B. Gudbjornsdottir, 1984. J. A ppl.Bacteriol., 57, 413-421. 21. Wang, M. Y., D. M. Ogrydziak, 1986. Appl.Environ. Microbiol., 52, 727-732.

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