Skip to main content
. 2020 Jul 7;20:198. doi: 10.1186/s12866-020-01876-7

Table 1.

Metabolism of 18:3n-3 and 18:2n-6a by different bacterial strains during 24 h of incubation under control growth conditions (Exp. 1). Blank cells related to 18:3n-3 and 18:2n-6 indicate no metabolism takes place by these strains

Strain Total VFA formed (μmol/tube; mean ± SD)b VFA productsc 18:3n-3 18:2n-6
% metabolized (mean ± SD)d Products formed (% of total intermediates formed and remaining 18:3n-3)e,f % metabolized (mean ± SD)d Products formed (% of total intermediates and remaining 18:2n-6)e,f
Acidaminococcus fermentans VR4 54 ± 9.5 A, B
Acidaminococcus intestini ADV 255.99 55 ± 13.0 A, B
Bifidobacterium adolescentis RU 424 251 ± 5.4 A 79.8 ± 13.94 10-OH ∆12,15–18:2 (45%) 76.8 ± 6.86 10-OH ∆12–18:1 (62%)
Bifidobacterium pseudolongum RU224 210 ± 18.5 A 26.7 ± 14.27 10-OH ∆12,15–18:2 (13%) 23.1 ± 8.56 10-OH ∆12–18:1 (15%)
Butyrivibrio fibrisolvens D1 102 ± 45.9 B, A 99.3 ± 0.43 c9,t11,c15 CLnA (48%) 98.0 ± 0.40 t11 18:1 (89%)
t11,c15 18:2 (43%)
t11 C18:1 (6%)
Butyrivibrio proteoclasticus P18 169 ± 12.7 B, A 98.9 ± 0.03 c9/t13/t14 18:1g (42%) 98.4 ± 0.48 18:0 (76%)
t15/c11 18:1g (21%) t11 18:1 (17%)
c15 18:1 (17%)
18:0 (6%)
t11, c15 18:2 (6%)
Lactobacillus ruminis RF1 30 ± 17.2 A, P
Lactobacillus ruminis RF2 14 ± 11.9 A, P
Cutibacterium acnes DSM 1897 99 ± 43.7 P, A 86.5 ± 15.83 ∆11,13,15–18:3 (50%) 88.4 ± 7.16 t10,c12 CLA (75%)
t10,c12,c15 CLnA (5%) 10-OH 12–18:1 (7%)
Ruminococcus albus 7 24 ± 8.6 A
Streptococcus equinus Pearl 11 18 ± 5.2 A 21.6 ± 10.58 13-OH ∆9,15–18:2 (6%) 84.0 ± 2.95 13-OH ∆9–18:1 (69%)
Streptococcus gallolyticus DSM 16831 16 ± 5.1 A 96.3 ± 1.49 13-OH ∆9,15–18:2 (86%) 89.8 ± 2.99 13-OH ∆9–18:1 (47%)
∆9,14–18:2 (32%)
Megasphaera elsdenii B159 147 ± 5.6 B
Megasphaera elsdenii T81 126 ± 6.1 B
Megasphaera elsdenii LC1 121 ± 11.2 B, A
Megasphaera elsdenii 2602A 191 ± 21.2 B, P 32.7 ± 8.92 13-OH ∆9,15–18:2 (19%) 81.8 ± 3.71 13-OH ∆9–18:1 (63%)
∆9,14–18:2 (5%)
Megasphaera elsdenii 3016B 138 ± 10.5 B
Megasphaera elsdenii 3218A 134 ± 7.9 B
Megasphaera elsdenii 3436A 117 ± 4.3 B
Megasphaera elsdenii 4251 125 ± 6.8 B
Megasphaera elsdenii 4257 124 ± 5.3 B
Megasphaera elsdenii 4296 120 ± 5.5 B
Megasphaera elsdenii 4400 58 ± 25.8 A, P
Megasphaera elsdenii 5045 128 ± 6.6 B
Megasphaera elsdenii 5052B 63 ± 9.9 A 60.9 ± 11.21 10-OH ∆12,15–18:2 (34%) 88.0 ± 2.20 13-OH ∆9–18:1 (42%)
10-OH ∆12–18:1 (24%)
Megasphaera elsdenii 5596 127 ± 3.1 B
Selenomonas ruminantium GA-192 83 ± 12.0 P, A
Selenomonas ruminantium PC 18 241 ± 31.8 P, A

a The initial amount of fatty acid was 40 μg/mL

b Measured fermentation products were acetate, propionate, isobutyrate, butyrate, isovalerate, valerate and caproate

c Main VFA product: A, acetate; B, butyrate; P, propionate; in decreasing order of importance. Lactate concentration was not measured

d % metabolized, proportion of the initial 18:3n-3 or 18:2n-6 which was converted after 24 h of incubation

e Only the intermediates representing ≥5% are presented as its proportion of the sum of total intermediates and remaining initial 18:3n-3 or 18:2n-6 after 24 h of incubation

fc, cis; t, trans; CLA, conjugated linoleic acid; CLnA, conjugated linolenic acid. For each of the formed intermediates, the proportion of the respective intermediate on the sum of total produced intermediates and remainder of the initial product (i.e. 18:3n-3 or 18:2n-6) after 24 h was calculated

g The different isomers could not be separated from each other with the used technique