Evaluation of chitoligosaccharides effect upon probiotic bacteria
The main objective of the present study was to evaluate the antibacterial effect – through the determination of minimum inhibitory (and lethal) concentrations, as well as the possible prebiotic potential of chitooligosaccharides (COS) – through the determination of growth curves, on Bifidobacterium...
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Published in | International journal of biological macromolecules Vol. 50; no. 1; pp. 148 - 152 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.01.2012
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Abstract | The main objective of the present study was to evaluate the antibacterial effect – through the determination of minimum inhibitory (and lethal) concentrations, as well as the possible prebiotic potential of chitooligosaccharides (COS) – through the determination of growth curves, on Bifidobacterium animalis Bb12, Bifidobacterium animalis Bo and Lactobacillus acidophilus Ki. Atomic force microscopy was further used to obtain high resolution images of COS effects upon the cell morphology. Our results demonstrate that COS do not stimulate the growth of those strains, neither the strains are capable of using COS as a primary source of carbon. Analysis of morphology when exposed to inhibitory/bactericidal concentrations, suggested that COS do not exert any direct damage upon the bacteria structure, instead the bacteria are apparently covered by COS, which likely prevent nutrient uptake. |
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AbstractList | The main objective of the present study was to evaluate the antibacterial effect - through the determination of minimum inhibitory (and lethal) concentrations, as well as the possible prebiotic potential of chitooligosaccharides (COS) - through the determination of growth curves, on Bifidobacterium animalis Bb12, Bifidobacterium animalis Bo and Lactobacillus acidophilus Ki. Atomic force microscopy was further used to obtain high resolution images of COS effects upon the cell morphology. Our results demonstrate that COS do not stimulate the growth of those strains, neither the strains are capable of using COS as a primary source of carbon. Analysis of morphology when exposed to inhibitory/bactericidal concentrations, suggested that COS do not exert any direct damage upon the bacteria structure, instead the bacteria are apparently covered by COS, which likely prevent nutrient uptake.The main objective of the present study was to evaluate the antibacterial effect - through the determination of minimum inhibitory (and lethal) concentrations, as well as the possible prebiotic potential of chitooligosaccharides (COS) - through the determination of growth curves, on Bifidobacterium animalis Bb12, Bifidobacterium animalis Bo and Lactobacillus acidophilus Ki. Atomic force microscopy was further used to obtain high resolution images of COS effects upon the cell morphology. Our results demonstrate that COS do not stimulate the growth of those strains, neither the strains are capable of using COS as a primary source of carbon. Analysis of morphology when exposed to inhibitory/bactericidal concentrations, suggested that COS do not exert any direct damage upon the bacteria structure, instead the bacteria are apparently covered by COS, which likely prevent nutrient uptake. The main objective of the present study was to evaluate the antibacterial effect - through the determination of minimum inhibitory (and lethal) concentrations, as well as the possible prebiotic potential of chitooligosaccharides (COS) - through the determination of growth curves, on Bifidobacterium animalis Bb12, Bifidobacterium animalis Bo and Lactobacillus acidophilus Ki. Atomic force microscopy was further used to obtain high resolution images of COS effects upon the cell morphology. Our results demonstrate that COS do not stimulate the growth of those strains, neither the strains are capable of using COS as a primary source of carbon. Analysis of morphology when exposed to inhibitory/bactericidal concentrations, suggested that COS do not exert any direct damage upon the bacteria structure, instead the bacteria are apparently covered by COS, which likely prevent nutrient uptake. |
Author | Eaton, Peter Fernandes, João C. Sousa, Sérgio Gomes, Ana Ramos, Óscar S. Santos-Silva, Alice Nascimento, Henrique Pintado, Manuela E. Xavier Malcata, F. Franco, Isabel |
Author_xml | – sequence: 1 givenname: João C. surname: Fernandes fullname: Fernandes, João C. email: jfernandes@email.com organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal – sequence: 2 givenname: Peter surname: Eaton fullname: Eaton, Peter organization: REQUIMTE, Departamento de Química, Faculdade de Ciências da Universidade do Porto, Rua do Campo Alegre, P-4169-007 Porto, Portugal – sequence: 3 givenname: Isabel surname: Franco fullname: Franco, Isabel organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal – sequence: 4 givenname: Óscar S. surname: Ramos fullname: Ramos, Óscar S. organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal – sequence: 5 givenname: Sérgio surname: Sousa fullname: Sousa, Sérgio organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal – sequence: 6 givenname: Henrique surname: Nascimento fullname: Nascimento, Henrique organization: Serviço de Bioquímica, Faculdade de Farmácia da Universidade do Porto, R. Aníbal Cunha, P-4050-047 Porto, Portugal – sequence: 7 givenname: Ana surname: Gomes fullname: Gomes, Ana organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal – sequence: 8 givenname: Alice surname: Santos-Silva fullname: Santos-Silva, Alice organization: Serviço de Bioquímica, Faculdade de Farmácia da Universidade do Porto, R. Aníbal Cunha, P-4050-047 Porto, Portugal – sequence: 9 givenname: F. surname: Xavier Malcata fullname: Xavier Malcata, F. organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal – sequence: 10 givenname: Manuela E. surname: Pintado fullname: Pintado, Manuela E. organization: CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal |
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Keywords | Probiotic bacteria Atomic force microscopy Chitosan Chitooligosaccharides |
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Snippet | The main objective of the present study was to evaluate the antibacterial effect – through the determination of minimum inhibitory (and lethal) concentrations,... The main objective of the present study was to evaluate the antibacterial effect - through the determination of minimum inhibitory (and lethal) concentrations,... |
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SubjectTerms | Anti-Bacterial Agents - chemistry antibacterial properties Atomic force microscopy bacteria Bifidobacterium - metabolism Bifidobacterium animalis carbon Carbon - chemistry cell biology Chitin - chemistry Chitooligosaccharides Chitosan Culture Media - chemistry Glucose - chemistry Hydrogen-Ion Concentration Lactobacillus acidophilus Lactobacillus acidophilus - metabolism Microbial Sensitivity Tests Microscopy, Atomic Force - methods nutrient uptake Oligosaccharides - chemistry prebiotics Probiotic bacteria probiotics Probiotics - metabolism Time Factors |
Title | Evaluation of chitoligosaccharides effect upon probiotic bacteria |
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