Lactobacillus plantarum and its biological implications

Introduction

Electron micrograph of L. plantarum

By Katie Adlam

At right is a sample image insertion. It works for any image uploaded anywhere to MicrobeWiki. The insertion code consists of:
Double brackets: [[
Filename: PHIL_1181_lores.jpg
Thumbnail status: |thumb|
Pixel size: |300px|
Placement on page: |right|
Legend/credit: Electron micrograph of the Ebola Zaire virus. This was the first photo ever taken of the virus, on 10/13/1976. By Dr. F.A. Murphy, now at U.C. Davis, then at the CDC.
Closed double brackets: ]]

Other examples:
Bold
Italic
Subscript: H₂O
Superscript: Fe³⁺

Lactobacillus plantarum (L. plantarum) is a rod-shaped, gram-positive lactic acid bacterium from the spirochete phylum. It is common found in the human and mammalian gastrointestinal tract and in saliva, as well as in various food products. It can grow at temperatures between 15-45˚C and at pH levels as low as 3.2 (1). L. plantarum is a facultative heterofermentative (2,3), which means that it ferments sugars to produce lactic acid, ethanol or acetic acid, and carbon dioxide under certain conditions and substrates. Depending on the carbon source, these bacteria can switch from using heterofermentative and homofermentative ways of metabolism. L. plantarum is a current interest to researchers and the food industry since it is considered a safe probiotic. This bacterium is acid and bile salt tolerant, which allows it to survive the passage through the gastrointestinal tract of humans.

Genome

Genome-atlas view of the L. plantarum WCFS1 chromosome, with the predicted origin of replication at the top. The outer to inner circles show (i) positive strand ORFs (red); (ii) negative strand ORFs (blue); (iii) GC-skew (green); (iv) G+C content (black); (v) prophage-related functions (green) and IS-like elements (purple); and (vi) rDNA operons (black) and tRNA encoding genes (red). Kleerebezem 2003.

L. plantarum has a relatively large genome compared to other Lactobacillus spp. Its genome consists of a 3.3 Mb chromosome, which is the largest sequenced genome of any lactic acid bacteria (2). The genome of L. plantarum consists of five rRNA operons, which are evenly distributed around the chromosome (FIGURE, 1). 62 tRNA encoding genes have been found and seem to be in relation to some of the rRNA clusters. In addition, the genome encodes two classes of transposase regions, which are thought to encode mobile genetic elements (1).

The genome consists of 3,052 protein-encoding genes and only 39 of these genes are pseudogenes (1). L. plantarum proteins are very similar to other Gram-positive bacteria since they have low GC content, have a peptidoglycan cell wall, and they are organized collinear. L. plantarum genome contains genes for the Embden-Meyerhoff-Parnas (EMP) pathway and some of the genes correlate to enzymes that break down pentoses and hexoses. Furthermore, its genome shows that it has genes that encode for phosphotransferase, mannose, and fructose systems (1).

Metabolism

Lactate and acetate production pathways in Lactobacillus plantarum. EMP, Embden–Meyerhof Parnas pathway; LDH, lactate dehydrogenase; POX, pyruvate oxidase; PDH, pyruvate dehydrogenase; PFL, pyruvate formate lyase; PTA, phosphotransacetylase; AK, acetate kinase. Quatravaux 2006.

L. plantarum is a facultative anaerobe or a facultative heterofermentative, as it can grow in the presence and absence of oxygen. It has enzymes for fermentation through the Embden-Meyerhoff-Parnas pathway (FIGURE) or through the phosphoketolase pathway, which allows this bacterium to perform homolactic and heterolactic fermentation (1). When oxygen is not present and this bacterium undergoes homolactic-like fermentation, L. plantarum converts carbon sources to D and L- forms of lactate and alcohols via lactate dehydrogenase. This normally occurs during its growth phase. It is important to note that L. plantarum can use a variety of carbon sources, which has been thought to be a result from horizontal gene transfer.

Under aerobic conditions, lactate is converted to acetate and one ATP is produced via lactate dehydrogenase, pyruvate oxidase, and acetate kinase enzymes. In addition to producing acetate, this pathway also forms hydrogen peroxide and carbon dioxide as byproducts. Hydrogen peroxide is formed by the conversion of oxygen via a manganese-dependent process and the production of this radical species can kill off other bacteria. Manganese-dependent processes use manganese as a catalase to lower the concentration of oxygen, which is beneficial to the aerotolerant bacterium (4). L. plantarum can produce a variety of products from fermentation due to a large “pyruvate-dissipating potential” (1). In addition, research has found that L. plantarum has a fumarate reductase, which implies that this bacterium has a basic electron transport chain (1). It is though that this bacterium possesses a nitrate reduction system, which could use nitrate as an electron acceptor. Furthermore, it does not possess the citric acid cycle, which is a cycle that aerobic organisms use to generate energy through oxidation of acetate.

Metabolism and Secretion

Schematic representation of the human gastrointestinal tract (GI tract) indicating its different regions where recombinant lactic acid bacteria (rLAB) encounter various challenges. Daniel 2011.

a) Effect of 16 and 62 cCFS on the growth of Rhodotorula mucilaginosa in orange juice. Control juice (), juice containing cCFS from Lactobacillus plantarum 16 (), juice containing cCFS from Lact. plantarum 62 (). P < 0·001 (***). (b) Effect of 16 and 62 cCFS on the growth of R. mucilaginosa in yoghurt. Control yoghurt (), yoghurt containing cCFS from Lact. plantarum 16 (), yoghurt containing cCFS from Lact. plantarum 62 (). P < 0·001 (***). Crowley 2012.

Hematoxylin-eosin stained gastric sections (×20). A: Control group showed normal gastric histopathology; B: Helicobacter pylori infected group showed infiltration of inflammatory cells (arrows); C and D: Lactobacillus plantarum (L. plantarum) B7 106 CFUs/mL treated and L. plantarum B7 1010 CFUs/mL treated groups showed improvements in gastric inflammation. GE: Gastric epithelium; LP: Lamina propria; MM: Muscularis mucosae; SM: Submucosa; ML: Muscularis.Sunanliganon 2012.

L. plantarum is typically found in a protein-rich environment, such as in yogurt, so it has uptake systems for peptides. Once these peptides are taken up, various types of peptidases degrade them. L. plantarum has 19 different genes encoding peptidases with different specific functions, three of which can cleave N-terminal proline residues. Even though this bacterium has protein degradation mechanisms, it is still capable of producing most amino acids, except branched-chain amino acids such as valine, leucine, and isoleucine (1).

In addition to synthesizing amino acids, L. plantarum also can perform a nonribosomal peptide synthesis (1). Before this discovery, no other lactic acid bacteria was known to use this sort of biosynthesis machinery. The L. plantarum nonribosomal peptide synthesis cluster contains two nonribosomal synthesis proteins, an important phosphopantetheinyl transferase, and proteins that are needed for precursors for regulation, transport, and enzymes (1).

Amino acids and peptides in L. plantarum are transported mainly through 57 ATP-binding cassette (ABC) transporters, which 27 are importers and 30 are exporters. Since this bacterium cannot synthesize its own branched chain amino acids, it is able to uptake them through these transporters. In addition, L. plantarum has a high number of sugar import systems and regulatory proteins, which could be responsible for how it is a flexible and versatile bacterium, as it can grow by using different carbon sources and can adapt to a wide array of environments (1).

L. plantarum is known to be able to adapt to stressful environments such as those with a low pH or high salt content. Its genome encodes for proteases that can degrade abnormal or nonfunctional proteins, as well as heat and cold-shock proteins to save energy under stress and to survive different climates. In order to survive in acidic environments, this bacterium uses the FoF1-ATPase and sodium-proton pumps to help regulate and maintain the intracellular pH. Furthermore, it has alkaline shock proteins to assist in pH tolerance. In addition, L. plantarum has developed ways to deal with oxidative stress by having catalases, peroxidases, and reductases, as well as a high intracellular concentration of manganese ions (Mn2+) to scavenge oxygen radicals (1). This bacterium is able to obtain and accumulate manganese ions due to the P-type manganese translocating ATPase.

In addition to being able to adapt to the environment, L. plantarum has surface proteins that allow it to interact with the environment. It has a Sec transport system that is comprised of SecA/SecE/SecG/SecY/YajC (no SecDF) and it also has other proteins involved in secretion such as peptidases (1). In addition, there are genes that encode for a sortase, which is an enzyme that recognizes and cleaves a carboxy-terminal sequences to modify the surface proteins to interact with different surfaces and substrates for growth. Lastly, L. plantarum has a protein machinery that is used to bind and uptake DNA from the environment. Because of this, scientists hypothesize that it acquired its ability to adapt to many different environments. They have found very large regions in genome of L. plantarum where there is unusual base composition when comparing to closely related species such as the genes for sugar uptake and catabolism (1). This reflects how L. plantarum is a very versatile species that can adjust to its environment.

.

Antibody response to oral administration of recombinant L. plantarum: mucosal IgA. del Rio 2010

Conclusion

Overall text length at least 3,000 words, with at least 3 figures.

References

Kleerebezem, M.; Boekhorst, J.; van Kranenburg, R.; Molenaar, D.; Kuipers, O. P.; Leer, R.; Tarchini, R.; Peters, S.A.; Sandbrink, H.M.; Fiers, M.W.E.J.; Stiekema, W.; Lankhorst, R.M.K.; Bron, P.A.; Hoffer, S.M.; Groot, M.N.N.; Kerkhoven, R.; de Vries, M.; Ursing, B.; de Vos, W.M.; Siezen, R.J. Complete genome sequence of Lactobacillus plantarum WCFS1. PNAS 2003, 100, 1990-1995.

Quatravaux, S.; Remize, F.; Bryckaert, E.; Colavizza, D.; Guzzo, J. Examination of Lactobacillus plantarum lactate metabolism side effects in relation to the modulation of aeration parameters. J Appl. Microbiol. 2006, 101, 903-912.

Daniel, C.; Roussel, Y.; Kleerebezem, M.; Pot, B. Recombinant lactic acid bacteria as mucosal biotherapeutic agents. Trends Biotechnol. 2011, 29, 499- 508.

Crowley, S.; Mahony, J.; van Sinderen, D. Comparative analysis of two antifungal Lactobacillus plantarum isolates and their application as bioprotectants in refrigerated foods. J. Appl. Microbiol. 2012, 113, 1417-1427.

Sunanliganon, C.; Thong-Ngam, D.; Tumwasorn, S.; Klaikeaw, N. Lactobacillus plantarum B7 inhibits Helicobacter pylori growth and attenuates gastric inflammation. World J Gastroenterol. 2012, 18, 2472-2480.

Rio, B.; Seegers, J.F.M.L.; Gomes-Solecki, M. Immune response of Lactobacillus plantarum expressing Borrelia burgdorferi OspA is modulated by the lipid modification of the antigen. PLoS ONE 2010, 5, e11199.

Edited by student of Joan Slonczewski for BIOL 238 Microbiology, 2011, Kenyon College.