Multidrug resistant pathogenic bacterial biofilm inhibition by Lactobacillus plantarum exopolysaccharide

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 315,771 · see citing works

Colorimetric Method for Determination of Sugars and Related Substances

DuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956) · Analytical Chemistry · doi:10.1021/ac60111a017 · Cited by 52,269 · see citing works

A PHOTOMETRIC ADAPTATION OF THE SOMOGYI METHOD FOR THE DETERMINATION OF GLUCOSE

Nelson, N. (1944) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)71980-7 · Cited by 10,376 · see citing works

Biofilm formation as microbial development

O'Toole, G., Kaplan, H. B., & Kolter, R. (2000) · Annual Review of Microbiology · doi:10.1146/annurev.micro.54.1.49 · Cited by 3,571 · see citing works

Microtiter Dish Biofilm Formation Assay

O’Toole, G. A. (2011) · Journal of Visualized Experiments · doi:10.3791/2437 · Cited by 2,184 · see citing works

Biofilm Formation: A Clinically Relevant Microbiological Process

Donlan, R. M. (2001) · Clinical Infectious Diseases · doi:10.1086/322972 · Cited by 1,343 · see citing works

A genetic basis for Pseudomonas aeruginosa biofilm antibiotic resistance

Mah, T., Pitts, B., Pellock, B. J., Walker, G. C., Stewart, P. S., & O’Toole, G. A. (2003) · Nature · doi:10.1038/nature02122 · Cited by 1,190 · see citing works

Biofilm formation in food industries: A food safety concern

Srey, S., Jahid, I. K., & Ha, S. (2012) · Food Control · doi:10.1016/j.foodcont.2012.12.001 · Cited by 1,005 · see citing works

<scp>d</scp> -Amino Acids Trigger Biofilm Disassembly

Kolodkin-Gal, I., Romero, D., Cao, S., Clardy, J., Kolter, R., & Losick, R. (2010) · Science · doi:10.1126/science.1188628 · Cited by 874 · see citing works

How microorganisms use hydrophobicity and what does this mean for human needs?

Krasowska, A., & Sigler, K. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00112 · Cited by 639 · see citing works

A Crucial Role for Exopolysaccharide Modification in Bacterial Biofilm Formation, Immune Evasion, and Virulence

Vuong, C., Kocianova, S., Voyich, J. M., Yao, Y., Fischer, E. R., DeLeo, F. R., & Otto, M. J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m411374200 · Cited by 592 · see citing works

Role of Exopolysaccharides in Pseudomonas aeruginosa Biofilm Formation and Architecture

Ghafoor, A., Hay, I. D., & Rehm, B. H. A. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.00637-11 · Cited by 535 · see citing works

Quorum sensing and social networking in the microbial world

Atkinson, S., & Williams, P. M. (2009) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0203 · Cited by 423 · see citing works

Antioxidant Activity of an Exopolysaccharide Isolated from Lactobacillus plantarum C88

Zhang, L., Liu, C., Li, D., Zhao, Y., Zhang, X., Zeng, X., Yang, Z., & Li, S. (2013) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2012.12.037 · Cited by 371 · see citing works

Production and purification of a novel exopolysaccharide from lactic acid bacterium Streptococcus phocae PI80 and its functional characteristics activity in vitro

Kanmani, P., Kumar, R., Yuvaraj, N., Paari, K. A., Pattukumar, V., & Arul, V. (2011) · Bioresource Technology · doi:10.1016/j.biortech.2010.12.118 · Cited by 295 · see citing works

Released exopolysaccharide (r-EPS) produced from probiotic bacteria reduce biofilm formation of enterohemorrhagic Escherichia coli O157:H7

Kim, Y., Oh, S., & Kim, S. H. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.053 · Cited by 276 · see citing works

Antibiofilm polysaccharides

Rendueles, O., Kaplan, J. B., & Ghigo, J. (2013) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02810.x · Cited by 271 · see citing works

Broad-spectrum biofilm inhibition by a secreted bacterial polysaccharide

Valle, J., Re, S. D., Henry, N., Fontaine, T., Balestrino, D., Latour‐Lambert, P., & Ghigo, J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605399103 · Cited by 258 · see citing works

The role of cell-surface interactions in bacterial initial adhesion and consequent biofilm formation on nanofiltration/reverse osmosis membranes

Habimana, O., Semião, A. J. C., & Casey, E. (2013) · Journal of Membrane Science · doi:10.1016/j.memsci.2013.11.043 · Cited by 257 · see citing works

The Cell Wall of Lactic Acid Bacteria: Surface Constituents and Macromolecular Conformations

Zammaretti, P., & Ubbink, J. (2003) · Biophysical Journal · doi:10.1016/s0006-3495(03)74820-6 · Cited by 250 · see citing works

Antioxidant activities of polysaccharides from Hyriopsis cumingii

Qiao, D., Ke, C., Hu, B., Luo, J., Ye, H., Sun, Y., Yan, X., & Zeng, X. (2009) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2009.03.018 · Cited by 242 · see citing works

Production, purification and structural characterization of an exopolysaccharide produced by a probiotic Lactobacillus plantarum MTCC 9510

Ismail, B., & Nampoothiri, K. M. (2010) · Archives of Microbiology · doi:10.1007/s00203-010-0636-y · Cited by 241 · see citing works

Purification and Characterization of Biofilm-Associated EPS Exopolysaccharides from ESKAPE Organisms and Other Pathogens

Bales, P. M., Renke, E. M., May, S. L., Shen, Y., & Nelson, D. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067950 · Cited by 232 · see citing works

Immunomodulatory and antioxidant potential of <i>Lactobacillus</i> exopolysaccharides

Liu, C., Tseng, K., Chiang, S., Lee, B., Hsu, W., & Pan, T. (2011) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.4456 · Cited by 230 · see citing works

Impact of the exopolysaccharide layer on biofilms, adhesion and resistance to stress in Lactobacillus johnsonii FI9785

Dertli̇, E., Mayer, M. J., & Narbad, A. (2015) · BMC Microbiology · doi:10.1186/s12866-015-0347-2 · Cited by 216 · see citing works

Inhibition of Vibrio biofilm formation by a marine actinomycete strain A66

You, J., Xue, X., Cao, L., Lü, X., Wang, J., Zhang, L., & Zhou, S. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-1074-x · Cited by 216 · see citing works

Biofilm formation: Hydrodynamic effects on internal diffusion and structure

Vieira, M. J., Melo, L. F., & Pinheiro, M. M. (1993) · Biofouling · doi:10.1080/08927019309386244 · Cited by 201 · see citing works

Mathematical Description of Microbial Biofilms

Klapper, I., & Dockery, J. D. (2010) · SIAM Review · doi:10.1137/080739720 · Cited by 198 · see citing works

Atomic Force Microscopy Study of the Effect of Antimicrobial Peptides on the Cell Envelope of <i>Escherichia coli</i>

Meincken, M., Holroyd, D. L., & Rautenbach, M. (2005) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.10.4085-4092.2005 · Cited by 192 · see citing works

Antibiofilm Approaches

Danese, P. N. (2002) · Chemistry & Biology · doi:10.1016/s1074-5521(02)00192-8 · Cited by 176 · see citing works

Antibiofilm Activity of an Exopolysaccharide from Marine Bacterium Vibrio sp. QY101

Jiang, P., Li, J., Han, F., Duan, G., Lu, X., Gu, Y., & Yu, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018514 · Cited by 165 · see citing works

Production of exopolysaccharides by Lactobacillus helveticus MB2-1 and its functional characteristics in vitro

Li, W., Ji, J., Rui, X., Yu, J., Tang, W., Chen, X., Jiang, M., & Dong, M. (2014) · LWT · doi:10.1016/j.lwt.2014.06.063 · Cited by 157 · see citing works

Anti-biofilm activity of an exopolysaccharide from a sponge-associated strain of Bacillus licheniformis

Sayem, S., Manzo, E., Ciavatta, M. L., Tramice, A., Cordone, A., Zanfardino, A., Felice, M. D., & Varcamonti, M. (2011) · Microbial Cell Factories · doi:10.1186/1475-2859-10-74 · Cited by 154 · see citing works

Structural characterization and bioactivity of released exopolysaccharides from Lactobacillus plantarum 70810

Wang, K., Li, W., Rui, X., Chen, X., Jiang, M., & Dong, M. (2014) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2014.02.056 · Cited by 150 · see citing works

Pseudomonas aeruginosa extracellular products inhibit staphylococcal growth, and disrupt established biofilms produced by Staphylococcus epidermidis

Qin, Z., Yang, L., Qu, D., Molin, S., & Tolker‐Nielsen, T. (2009) · Microbiology · doi:10.1099/mic.0.028001-0 · Cited by 140 · see citing works

Surface Recognition among Oral Bacteria: Multigeneric Coaggregations and their Mediators

Kolenbrander, P. E. (1989) · Critical Reviews in Microbiology · doi:10.3109/10408418909105746 · Cited by 136 · see citing works

Relationship between Expression of the Family of M Proteins and Lipoteichoic Acid to Hydrophobicity and Biofilm Formation in Streptococcus pyogenes

Courtney, H. S., Ofek, I., Penfound, T. A., Nizet, V., Pence, M. A., Kreikemeyer, B., Podbielbski, A., Hasty, D. L., & Dale, J. B. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004166 · Cited by 128 · see citing works

Atomic force microscopy study of the antimicrobial action of Sushi peptides on Gram negative bacteria

Li, A. A., Lee, P. Y., Ho, B., Ding, J. L., & Lim, C. T. (2006) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2006.12.010 · Cited by 103 · see citing works

Broad-Spectrum Biofilm Inhibition by Kingella kingae Exopolysaccharide

Bendaoud, M., VINOGRADOV, E. V., Balashova, N. V., Kadouri, D. E., Kachlany, S. C., & Kaplan, J. B. (2011) · Journal of Bacteriology · doi:10.1128/jb.00311-11 · Cited by 101 · see citing works

Role of type 1 fimbriae and mannose in the development ofEscherichia coliK12 biofilm: from initial cell adhesion to biofilm formation

Rodrigues, D. F., & Elimelech, M. (2009) · Biofouling · doi:10.1080/08927010902833443 · Cited by 93 · see citing works

Cell-surface hydrophobicity of adherent oral bacteria

Weiss, E. I., Rosenberg, M., Judes, H., & ROSENBERG, E. B. (1982) · Current Microbiology · doi:10.1007/bf01568427 · Cited by 86 · see citing works

Molecular Weight and Monosaccharide Composition of Astragalus Polysaccharides

Xu, D., Xia, Q., Wang, J., & Wang, P.-P. (2008) · Molecules · doi:10.3390/molecules13102408 · Cited by 78 · see citing works

Promising biotechnological applications of antibiofilm exopolysaccharides

Bernal, P., & Llamas, M. A. (2012) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2012.00359.x · Cited by 73 · see citing works

Inhibition of pathogenic and spoilage bacteria by a novel biofilm-forming Lactobacillus isolate: a potential host for the expression of heterologous proteins

Jalilsood, T., Baradaran, A., Song, A. A., Foo, H. L., Mustafa, S., Saad, W. Z., Yusoff, K., & Rahim, R. A. (2015) · Microbial Cell Factories · doi:10.1186/s12934-015-0283-8 · Cited by 56 · see citing works

Effect of Varidase (Streptokinase) on Biofilm Formed by Staphylococcus aureus

Nemoto, K., Hirota, K., Ono, T., Murakami, K., Murakami, K., Nagao, D., & Miyake, Y. (2000) · Chemotherapy · doi:10.1159/000007264 · Cited by 54 · see citing works

Lethality of Chlorine, Chlorine Dioxide, and a Commercial Produce Sanitizer to Bacillus cereus and Pseudomonas in a Liquid Detergent, on Stainless Steel, and in Biofilm

Kreske, A. C., Ryu, J., Pettigrew, C. A., & Beuchat, L. R. (2006) · Journal of Food Protection · doi:10.4315/0362-028x-69.11.2621 · Cited by 43 · see citing works

Conflicting roles for a cell surface modification in S almonella

May, J. F., & Groisman, E. A. (2013) · Molecular Microbiology · doi:10.1111/mmi.12236 · Cited by 26 · see citing works

Escherichia coli Resistance to Nonbiocidal Antibiofilm Polysaccharides Is Rare and Mediated by Multiple Mutations Leading to Surface Physicochemical Modifications

Travier, L., Rendueles, O., Ferrières, L., Herry, J., & Ghigo, J. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02606-12 · Cited by 26 · see citing works

Link between Culture Zeta Potential Homogeneity and Ebp in Enterococcus faecalis

Tariq, M., Bruijs, C., Kok, J., & Krom, B. P. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.07618-11 · Cited by 22 · see citing works

Influence of Surface Zeta Potential on Adhesion of Chlorella sp. to Substratum Surfaces

Zhang, X. R., Jiang, Z. Y., Yuan, H., Lu, Y. X., Chen, L., Chou, A., Yan, H., & Zhang, X. X. (2013) · Advanced materials research · doi:10.4028/www.scientific.net/amr.690-693.1431 · Cited by 6 · see citing works

The use of bacterial polysaccharides in bioprinting

McCarthy, R. R., Ullah, M. W., Booth, P., Pei, E., & Yang, G. (2019) · Biotechnology Advances · doi:10.1016/j.biotechadv.2019.107448 · Cited by 115 · see citing works

Preparation, Partial Characterization and Biological Activity of Exopolysaccharides Produced from Lactobacillus fermentum S1

Wang, K., Niu, M., Song, D., Song, X., Zhao, J., Wu, Y., Lu, B., & Niu, G. (2020) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2019.07.009 · Cited by 110 · see citing works

Antibiotic Resistance Crisis: An Update on Antagonistic Interactions between Probiotics and Methicillin-Resistant Staphylococcus aureus (MRSA)

Nataraj, B. H., & Mallappa, R. H. (2021) · Current Microbiology · doi:10.1007/s00284-021-02442-8 · Cited by 83 · see citing works

Feeding Lactic Acid Bacteria with Different Sugars: Effect on Exopolysaccharides (EPS) Production and Their Molecular Characteristics

Fuso, A., Bancalari, E., Castellone, V., Caligiani, A., Gatti, M., & Bottari, B. (2023) · Foods · doi:10.3390/foods12010215 · Cited by 57 · see citing works

Prebiotic potential of water extractable polysaccharide from red kidney bean (Phaseolus vulgaris L.)

Jabastin, J., Devi, P. B., Kavitake, D., Priyadarisini, V. B., & Shetty, P. H. (2018) · LWT · doi:10.1016/j.lwt.2018.11.089 · Cited by 50 · see citing works

Antipathogenic potentials of exopolysaccharides produced by lactic acid bacteria and their food and health applications

Kavitake, D., Tiwari, S., Shah, I. A., Devi, P. B., Delattre, C., Reddy, G. B., & Shetty, P. H. (2023) · Food Control · doi:10.1016/j.foodcont.2023.109850 · Cited by 41 · see citing works

Anti-Helicobacter pylori Activity of a Lactobacillus sp. PW-7 Exopolysaccharide

Hu, J., Tian, X., Wei, T., Wu, H., Lü, J., Lyu, M., & Wang, S. (2021) · Foods · doi:10.3390/foods10102453 · Cited by 27 · see citing works

Analysis of Chemical Structure and Antibiofilm Properties of Exopolysaccharides from Lactiplantibacillus plantarum EIR/IF-1 Postbiotics

Karaca, B., Haliscelik, O., Gursoy, M., Kiran, F., Loimaranta, V., Söderling, E., & Gursoy, U. K. (2022) · Microorganisms · doi:10.3390/microorganisms10112200 · Cited by 26 · see citing works

Biobased Anti-Adhesive Marine Coatings from Polyhydroxyalkanoates and Polysaccharides

Faÿ, F., Champion, M., Guennec, A., Moppert, X., Simon‐Colin, C., & Elie, M. P. (2023) · Coatings · doi:10.3390/coatings13040766 · Cited by 21 · see citing works

Characterization of Exopolysaccharides from Lactiplantibacillus plantarum PC715 and Their Antibiofilm Activity Against Hafnia alvei

Tan, X., Ma, B., Wang, X., Cui, F., Li, X., & Li, J. (2024) · Microorganisms · doi:10.3390/microorganisms12112229 · Cited by 20 · see citing works

Development of coconut water-based exopolysaccharide rich functional beverage by fermentation with probiotic Lactobacillus plantarum SVP2

Goveas, L. C., Ashwath, K., Nazerath, B. R., Dsouza, O., Ullekh, Umesh, A., & Vidya, S. M. (2021) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2021.102030 · Cited by 14 · see citing works

Characterization and antifouling activity analysis of extracellular polymeric substances produced by an epibiotic bacterial strain Kocuria flava associated with the green macroalga Ulva lactuca

Ba-Akdah, M. A., & Satheesh, S. (2021) · Acta Oceanologica Sinica · doi:10.1007/s13131-020-1694-x · Cited by 14 · see citing works

Probiotic cell wall components as emerging postbiotics: structural diversity, immunoregulatory mechanisms, and health applications

Ding, L., Yin, J., Liu, J., Zou, J., Liu, J., Jin, Y., Tu, M., Li, P., Gu, Q., & Han, J. (2026) · Food & Function · doi:10.1039/d6fo00491a · Cited by 10 · see citing works

Optimization, structural characterization, and biological applications of exopolysaccharide produced by Enterococcus faecium KT990028

de Brito, L. P., da Silva, E. C., Lins, L. F., de Medeiros, R. S., Silva, F. C. O., Pastrana, L. M., Cavalcanti, I. D. L., Nogueira, M. C. D. B. L., Cavalcanti, M. T. H., & Porto, A. L. F. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136926 · Cited by 9 · see citing works

Bioconversion of sugar beet molasses into functional exopolysaccharides by beet juice-derived lactic acid bacteria

Ren, G., Luo, W., Gan, H., Zhang, H., Hou, X., Li, S., Chen, A., Zhang, Z., Le, P., Zhao, S., et al. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105139 · Cited by 8 · see citing works

Lactobacillus-derived components for inhibiting biofilm formation in the food industry

Li, J., Zhang, Q., Zhao, J., Zhang, H., & Chen, W. (2024) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-024-03933-z · Cited by 10 · see citing works

Biosurfactant from Lactobacillus sp. as an antibiofilm agent

Kaur, S., & Kaur, R. (2019) · Biotechnologia · doi:10.5114/bta.2019.87591 · Cited by 8 · see citing works

Biosurfactant Production and its Role in Candida albicans Biofilm Inhibition

Kaur, D. M., Patil, R., & Saima, A. (2020) · Journal of Pure and Applied Microbiology · doi:10.22207/jpam.14.2.30 · Cited by 8 · see citing works

Polysaccharide Galactan Inhibits Pseudomonas aeruginosa Biofilm Formation but Protects Pre-formed Biofilms from Antibiotics

Av, G., & Karyagina, A. S. (2019) · Biochemistry (Moscow) · doi:10.1134/s0006297919050055 · Cited by 6 · see citing works

Electrostatically assembled maghemite nanoparticles-Lactobacillus plantarum: A novel hybrid for enhanced antioxidant, antimicrobial, and antibiofilm efficacy

Shingade, J. A., Padalkar, N. S., Shin, J. H., Kim, Y. H., Park, T. J., Park, J. P., & PATIL, A. R. (2025) · Bioresource Technology · doi:10.1016/j.biortech.2025.132538 · Cited by 5 · see citing works

Probiotic Lactobacillus plantarum SVP2 fermented bioactive EPS-rich milk whey functional beverage

Goveas, L. C., Darshini, S. M., Kausthubha, P., Padyana, S., Anvitha, Suvarna, A. R., Lewis, S. P., & Vidya, S. M. (2024) · Journal of Food Science and Technology · doi:10.1007/s13197-024-06126-6 · Cited by 5 · see citing works

Characterization and immunomodulatory activity of exopolysaccharides produced by Lacticaseibacillus casei strains on macrophage cultures

Seftiarini, W., Pratiwi, R., Siregar, A. R., Nguyen, T., & Widodo, W. (2025) · Food Science and Biotechnology · doi:10.1007/s10068-025-02010-x · Cited by 4 · see citing works

Immunomodulatory and radioprotective property of glucans isolated from lactobacillus species

Pradeepa, Umesh, A., Manasadeepika, Manjunath, A., Salian, C., Darshini, S. M., Prabhakar, B. T., Mutalik, S., Manjunatha, B. K., & Vidya, S. M. (2021) · Bioactive Carbohydrates and Dietary Fibre · doi:10.1016/j.bcdf.2021.100304 · Cited by 3 · see citing works

Inhibitory effect of preformed Lactiplantibacillus plantarum biofilm against Clostridium perfringens biofilm formation on stainless steel surfaces

Zhang, Z., Luo, H., Chen, C., Xu, B., & Li, P. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.105966 · Cited by 2 · see citing works

Antibiofilm potential of Lactobacillus paraprobiotics and postbiotics: sustainable alternatives to antimicrobials

Malik, H. N., Kumar, P., & Ray, S. (2026) · Journal of Applied Microbiology · doi:10.1093/jambio/lxag078 · Cited by 2 · see citing works

A Fucose-containing Hetero-exopolysaccharide From Levilactobacillus brevis B151 Exhibits Potent Antimicrobial, Antibiofilm, and Antioxidant Activities

Yadav, M. K., Mendoza, R. M., Song, J. H., Vasquez, R., Lee, J. S., Park, Y., Paik, H., Kim, I. H., & Kang, D. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10835-5 · Cited by 1 · see citing works

Convenient framework of poly functionalized (E)-2-benzylideno-(Z)-carbazolylideno cyanoacetamides via rearrangements as an efficient antibiofilm inhibitors with SAR study

Sathiyachandran, P., Jayamanoharan, J., Nesterov, V. N., & Prasad, K. J. R. (2019) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2019.01.015 · Cited by 1 · see citing works

Screening functional ingredients for the prevention of diarrhoea caused by etec k88 in miniaturized models

Zhu, Y. (2018) · Dialnet (Universidad de la Rioja)

Anti-biofilm and anti-cancer effects of biosurfactant from Lactobacillus plantarum SVP2 in fermented milk whey beverage

Goveas, L. C., Khanapur, P., Chetan, D. M., Nannuri, K., Shishir, R. K., Murugesan, G., Rao, R. N., Selvaraj, R., Vinayagam, R., & Vidya, S. M. (2025) · Journal of Food Science and Technology · doi:10.1007/s13197-025-06306-y

Biological and chemical study of exopolysaccharides produced by marine microorganisms and its effect on arthritis

Awady, M. E. E., Hamed, A. A., Selim, M. S., Selim, H. M. R. M., Gomaa, F. A. M., Moustafa, N. M., El-Wakil, E. S., Mohamed, S. S., & Ghareeb, M. A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-26771-0.00034-5

Quorum quenching pathoblockers from bacteria: an alternative approach for bacterial infection management

Vijayan, N. K., Tanimu, H., & Sukumaran, B. O. (2025) · Folia Microbiologica · doi:10.1007/s12223-025-01395-w

Inhibition of Staphylococcus epidermidis Biofilm Formation by a Synthetic Breitfussin Analogue

Heimböck, M. P., Hansen, K. Ø., Guttormsen, Y., Pandey, S. K., Johnsen, E., Haug, B. E., Bayer, A., Sánchez, P., Petit, G. A., Hansen, E. H., et al. (2026) · Microbiology Research · doi:10.3390/microbiolres17060105

Antibiofilm Effect of Subtilisin and Fungal EPS against the Biofilm of Brevundimonas faecalis BC1 Collected from Monumental Rock

Samal, S. K., Acharya, D., & Sahoo, D. (2026) · Microbiology · doi:10.1134/s0026261725604233

Analysis of Chemical Structure and Antibiofilm Properties of Exopolysaccharides from Lactiplantibacillus plantarum EIR/IF-1 Postbiotics

Karaca, B., Haliscelik, O., Gursoy, M., Kiran, F., Loimaranta, V., Söderling, E., & Gursoy, U. K. (2022) · Microorganisms · doi:10.3390/microorganisms10112200 · Cited by 26 · see citing works

Extracellular polysaccharide derived from potential probiotic strain with antioxidant and antibacterial activities as a prebiotic agent to control pathogenic bacterial biofilm formation

Mahdhi, A., Leban, N., Chakroun, I., Chaouch, M. A., Hafsa, J., Fdhila, K., Mahdouani, K., & Majdoub, H. (2017) · Microbial Pathogenesis · doi:10.1016/j.micpath.2017.05.046 · Cited by 90 · see citing works

Assessment of anti-biofilm activity and bifidogenic growth stimulator (BGS) effect of lyophilized exopolysaccharides (l-EPSs) from <i>Lactobacilli</i> strains

Sarikaya, H., Aslim, B., & Yuksekdag, Z. (2017) · International Journal of Food Properties · doi:10.1080/10942912.2016.1160923 · Cited by 65 · see citing works

Extraction and characterization of exopolysaccharides from Lactiplantibacillus plantarum strain PRK7 and PRK 11, and evaluation of their antioxidant, emulsion, and antibiofilm activities

Kowsalya, M., Velmurugan, T., Mythili, R., Kim, W., Sudha, K. G., Ali, S., Kalpana, B., Ramalingam, S., & Rajeshkumar, M. P. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.124842 · Cited by 29 · see citing works

Characterization of Exopolysaccharides from Lactiplantibacillus plantarum PC715 and Their Antibiofilm Activity Against Hafnia alvei

Tan, X., Ma, B., Wang, X., Cui, F., Li, X., & Li, J. (2024) · Microorganisms · doi:10.3390/microorganisms12112229 · Cited by 20 · see citing works