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Effect of pH on Conjugated Linoleic Acid (CLA) Formation of Linolenic Acid Biohydrogenation by Ruminal Microorganisms
Yongjae Lee
J. Microbiol. 2013;51(4):471-476.   Published online August 30, 2013
DOI: https://doi.org/10.1007/s12275-013-1070-z
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AbstractAbstract
Conventional beliefs surrounding the linolenic acid (LNA; cis-9 cis-12 cis-15 C18:3) biohydrogenation (BH) pathway propose that it converts to stearic acid (SA) without the formation of conjugated linoleic acid (CLA) as intermediate isomers. However, an advanced study (Lee and Jenkins, 2011) verified that LNA BH yields multiple CLAs. This study utilized the stable isotope tracer to investigate the BH intermediates of 13C-LNA with different pH conditions (5.5 and 6.5). The 13C enrichment was calculated as a 13C/12C ratio of labeled minus unlabeled. After 24 h, eight CLA isomers were significantly enriched on both pH treatment, this result verifies that these CLAs originated from 13C-LNA BH which supports the results of Lee and Jenkins (2011). The enrichment of cis-cis double bond CLAs (cis-9 cis-11 and cis-10 cis-12 CLA) were significantly higher at low pH conditions. Furthermore, the concentration of cis-10 cis-12 CLA at low pH was four times higher than at high pH conditions after a 3 h incubation. These differences support the LNA BH pathways partial switch under different pH conditions, with a strong influence on the cis-cis CLA at low pH. Several mono-, di-, and tri-enoic fatty acid isomers were enriched during 24 h of incubation, but the enrichment was decreased or restricted at low pH treatment. Based on these results, it is proposed that low pH conditions may cause a changed or limited capacity of the isomerization and reduction steps in BH.

Citations

Citations to this article as recorded by  
  • Invited review: Research on ruminal biohydrogenation—Achievements, gaps in knowledge, and future approaches from the perspective of dairy science
    P.G. Toral, G. Hervás, P. Frutos
    Journal of Dairy Science.2024; 107(12): 10115.     CrossRef
  • Selenate and selenite affect ruminal metabolism of C18 unsaturated fatty acids and fatty acid composition of lamb tissues
    Małgorzata Białek, Marian Czauderna, Wiesław Przybylski, Danuta Jaworska
    Livestock Science.2020; 241: 104249.     CrossRef
  • Effects of Supplementation of Rumen Protected Fats on Rumen Ecology and Digestibility of Nutrients in Sheep
    Atique A. Behan, Teck Chwen Loh, Sharida Fakurazi, Ubedullah Kaka, Asmatullah Kaka, Anjas Asmara Samsudin
    Animals.2019; 9(7): 400.     CrossRef
  • In vitro biohydrogenation of 13C-labeled α-linolenic acid in response to ruminal alterations associated with diet-induced milk fat depression in ewes
    P.G. Toral, G. Hervás, P. Frutos
    Journal of Dairy Science.2019; 102(2): 1213.     CrossRef
  • Accumulation of conjugated linoleic acid in Lactobacillus plantarum WU-P19 is enhanced by induction with linoleic acid and chitosan treatment
    Wilawan Palachum, Wanna Choorit, Yusuf Chisti
    Annals of Microbiology.2018; 68(10): 611.     CrossRef
  • The In vitro Effects of Nano-encapsulated Conjugated Linoleic Acid on Stability of Conjugated Linoleic Acid and Fermentation Profiles in the Rumen
    Wan Heo, Eun Tae Kim, Sung Do Cho, Jun Ho Kim, Seong Min Kwon, Ha Yeon Jeong, Kwang Seok Ki, Ho Baek Yoon, Young Dae Ahn, Sung Sill Lee, Young Jun Kim
    Asian-Australasian Journal of Animal Sciences.2016; 29(3): 365.     CrossRef
  • Sources and Bioactive Properties of Conjugated Dietary Fatty Acids
    Alan A. Hennessy, Paul R. Ross, Gerald F. Fitzgerald, Catherine Stanton
    Lipids.2016; 51(4): 377.     CrossRef
  • Influence of Carotino oil on in vitro rumen fermentation, metabolism and apparent biohydrogenation of fatty acids
    Kazeem Dauda Adeyemi, Mahdi Ebrahimi, Anjas Asmara Samsudin, Abd Razak Alimon, Roselina Karim, Saiful Anuar Karsani, Awis Qurni Sazili
    Animal Science Journal.2015; 86(3): 270.     CrossRef
  • Seleno‐methionine decreases biohydrogenation of C18 unsaturated fatty acids in ovine ruminal fluid incubated in vitro with α‐linolenic acid
    Marian Czauderna, Agnieszka J. Rozbicka‐Wieczorek, Edyta Więsyk, Katarzyna A. Krajewska‐Bienias
    European Journal of Lipid Science and Technology.2015; 117(6): 820.     CrossRef
Research Support, Non-U.S. Gov't
Isolation and Characterization of a Rhodococcus Species Strain Able to Grow on ortho- and para-Xylene
Jung Yeon Jang , Dockyu Kim , Hyun Won Bae , Ki Young Choi , Jong-Chan Chae , Gerben J. Zylstra , Young Min Kim , Eungbin Kim
J. Microbiol. 2005;43(4):325-330.
DOI: https://doi.org/2258 [pii]
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AbstractAbstract
Rhodococcus sp. strain YU6 was isolated from soil for the ability to grow on o-xylene as the sole carbon and energy source. Unlike most other o-xylene-degrading bacteria, YU6 is able to grow on p-xylene. Numerous growth substrate range experiments, in addition to the ring-cleavage enzyme assay data, suggest that YU6 initially metabolizes o- and p-xylene by direct aromatic ring oxidation. This leads to the formation of dimethylcatechols, which was further degraded largely through meta-cleavage pathway. The gene encoding meta-cleavage dioxygenase enzyme was PCR cloned from genomic YU6 DNA using previously known gene sequence data from the o-xylene-degrading Rhodococcus sp. strain DK17. Subsequent sequencing of the 918-bp PCR product revealed a 98% identity to the gene, encoding methylcatechol 2,3-dioxygenase from DK17. PFGE analysis followed by Southern hybridization with the catechol 2,3-dioxygenase gene demonstrated that the gene is located on an approximately 560-kb megaplasmid, designated pJYJ1 <br>

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