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Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid
The linoleic acid isomerase enzyme from Propionibacterium acnes responsible for bioconversion of linoleic acid to trans-10, cis-12 conjugated linoleic acid (t10, c12 CLA) was cloned and overexpressed in Lactococcus lactis and Escherichia coli, resulting in between 30 and 50 % conversion rates of the...
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Formato: | Texto |
Lenguaje: | English |
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Microbiology Society
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885616/ https://www.ncbi.nlm.nih.gov/pubmed/17660413 http://dx.doi.org/10.1099/mic.0.2006/001966-0 |
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author | Rosberg-Cody, Eva Johnson, Mark C. Fitzgerald, Gerald F. Ross, Paul R. Stanton, Catherine |
author_facet | Rosberg-Cody, Eva Johnson, Mark C. Fitzgerald, Gerald F. Ross, Paul R. Stanton, Catherine |
author_sort | Rosberg-Cody, Eva |
collection | PubMed |
description | The linoleic acid isomerase enzyme from Propionibacterium acnes responsible for bioconversion of linoleic acid to trans-10, cis-12 conjugated linoleic acid (t10, c12 CLA) was cloned and overexpressed in Lactococcus lactis and Escherichia coli, resulting in between 30 and 50 % conversion rates of the substrate linoleic acid to t10, c12 CLA. The anti-proliferative activities of the fatty acids produced following isomerization of linoleic acid by L. lactis and E. coli were assessed using the human SW480 colon cancer cell line. Fatty acids generated from both L. lactis and E. coli contained a mixture of linoleic acid and t10, c12 CLA at a ratio of ∼1.35 : 1. Following 5 days of incubation of SW480 cells with 5–20 μg ml(−1) (17.8–71.3 μM) of the t10, c12 CLA, there was a significant (P<0.001) reduction in growth of the SW480 cancer cells compared with the linoleic acid control. Cell viability after treatment with the highest concentration (20 μg ml(−1)) of the t10, c12 CLA was reduced to 7.9 % (L. lactis CLA) and 19.6 % (E. coli CLA), compared with 95.4 % (control linoleic acid) and 31.7 % (pure t10, c12 CLA). In conclusion, this is believed to represent the first report in which recombinant strains are capable of producing CLA with an anti-proliferative potential. |
format | Text |
id | pubmed-2885616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-28856162010-07-06 Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid Rosberg-Cody, Eva Johnson, Mark C. Fitzgerald, Gerald F. Ross, Paul R. Stanton, Catherine Microbiology (Reading) Biochemistry and Molecular Biology The linoleic acid isomerase enzyme from Propionibacterium acnes responsible for bioconversion of linoleic acid to trans-10, cis-12 conjugated linoleic acid (t10, c12 CLA) was cloned and overexpressed in Lactococcus lactis and Escherichia coli, resulting in between 30 and 50 % conversion rates of the substrate linoleic acid to t10, c12 CLA. The anti-proliferative activities of the fatty acids produced following isomerization of linoleic acid by L. lactis and E. coli were assessed using the human SW480 colon cancer cell line. Fatty acids generated from both L. lactis and E. coli contained a mixture of linoleic acid and t10, c12 CLA at a ratio of ∼1.35 : 1. Following 5 days of incubation of SW480 cells with 5–20 μg ml(−1) (17.8–71.3 μM) of the t10, c12 CLA, there was a significant (P<0.001) reduction in growth of the SW480 cancer cells compared with the linoleic acid control. Cell viability after treatment with the highest concentration (20 μg ml(−1)) of the t10, c12 CLA was reduced to 7.9 % (L. lactis CLA) and 19.6 % (E. coli CLA), compared with 95.4 % (control linoleic acid) and 31.7 % (pure t10, c12 CLA). In conclusion, this is believed to represent the first report in which recombinant strains are capable of producing CLA with an anti-proliferative potential. Microbiology Society 2007-08 /pmc/articles/PMC2885616/ /pubmed/17660413 http://dx.doi.org/10.1099/mic.0.2006/001966-0 Text en Copyright © 2007, SGM http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biochemistry and Molecular Biology Rosberg-Cody, Eva Johnson, Mark C. Fitzgerald, Gerald F. Ross, Paul R. Stanton, Catherine Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
title | Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
title_full | Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
title_fullStr | Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
title_full_unstemmed | Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
title_short | Heterologous expression of linoleic acid isomerase from Propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
title_sort | heterologous expression of linoleic acid isomerase from propionibacterium acnes and anti-proliferative activity of recombinant trans-10, cis-12 conjugated linoleic acid |
topic | Biochemistry and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885616/ https://www.ncbi.nlm.nih.gov/pubmed/17660413 http://dx.doi.org/10.1099/mic.0.2006/001966-0 |
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