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| Indexado |
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| DOI | 10.1128/MMBR.00019-18 | ||||
| Año | 2018 | ||||
| Tipo | revisión |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Conjugated linoleic acids (CLAs) and conjugated linolenic acids (CLNAs) have gained significant attention due to their anticarcinogenic and lipid/energy metabolism-modulatory effects. However, their concentration in foodstuffs is insufficient for any therapeutic application to be implemented. From a biotechnological standpoint, microbial production of these conjugated fatty acids (CFAs) has been explored as an alternative, and strains of the genera Propionibacterium, Lactobacillus, and Bifidobacterium have shown promising producing capacities. Current screening research works are generally based on direct analytical determination of production capacity (e.g., trial and error), representing an important bottleneck in these studies. This review aims to summarize the available information regarding identified genes and proteins involved in CLA/CLNA production by these groups of bacteria and, consequently, the possible enzymatic reactions behind such metabolic processes. Linoleate isomerase (LAI) was the first enzyme to be described to be involved in the microbiological transformation of linoleic acids (LAs) and linolenic acids (LNAs) into CFA isomers. Thus, the availability of lai gene sequences has allowed the development of genetic screening tools. Nevertheless, several studies have reported that LAIs have significant homology with myosin-cross-reactive antigen (MCRA) proteins, which are involved in the synthesis of hydroxy fatty acids, as shown by hydratase activity. Furthermore, it has been suggested that CLA and/or CLNA production results from a stress response performed by the activation of more than one gene in a multiple-step reaction. Studies on CFA biochemical pathways are essential to understand and characterize the metabolic mechanism behind this process, unraveling all the gene products that may be involved. As some of these bacteria have shown modulation of lipid metabolism in vivo, further research to be focused on this topic may help us to understand the role of the gut microbiota in human health.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Salsinha, Ana Sofia | Mujer |
Univ Catolica Portuguesa - Portugal
Universidade Católica Portuguesa - Portugal |
| 2 | Pimentel, Ligia Leao | Mujer |
Univ Catolica Portuguesa - Portugal
Univ Porto - Portugal Univ Aveiro - Portugal Universidade Católica Portuguesa - Portugal Universidade do Porto - Portugal Universidade de Aveiro - Portugal Faculdade de Medicina da Universidade do Porto (FMUP) - Portugal |
| 3 | Fontes, Ana Luiza | Mujer |
Univ Catolica Portuguesa - Portugal
Univ Aveiro - Portugal Universidade Católica Portuguesa - Portugal Universidade de Aveiro - Portugal |
| 4 | Gomes, Ana Maria | Mujer |
Univ Catolica Portuguesa - Portugal
Universidade Católica Portuguesa - Portugal |
| 5 | Rodriguez-Alcala, Luis Miguel | Hombre |
Univ Catolica Portuguesa - Portugal
Universidad Bernardo O'Higgins - Chile Universidade Católica Portuguesa - Portugal |
| Fuente |
|---|
| Fundação para a Ciência e a Tecnologia |
| FCT |
| Portuguese government through the FCT |
| national funds via the Fundacao para a Ciencia e a Tecnologia (FCT), under the project Pro-TECh-CLnA-Microbial Production of Bioactive Conjugated Linolenic Acid Isomers To Obtain Functional Ingredients and Foods |
| Agradecimiento |
|---|
| This work was financed by national funds via the Fundacao para a Ciencia e a Tecnologia (FCT), under the project Pro-TECh-CLnA-Microbial Production of Bioactive Conjugated Linolenic Acid Isomers To Obtain Functional Ingredients and Foods (reference PTDC/AGR-TEC/2125/2014). Financial support for L.L.P. and A.L.F. was provided by fellowships SFRH/BPD/119785/2016 and SFRH/BD/117721/2016, respectively, granted by the Portuguese government through the FCT. We also acknowledge the scientific collaboration under FCT project UID/Multi/50016/2013. |