TABLE 1.
Substrate | Activity in biolog platesa | Root exudatesb | Leaf exudatesb |
---|---|---|---|
l-Arabinose | 382 ± 33 | + | + |
l-Fucose | 445 ± 41 | +c | +c |
α-d-Glucose | 74 ± 22 | + | + |
α-Hydroxybutyric acid | 871 ± 47 | + | NRd |
Succinic acid | 196 ± 20 | + | + |
l-Asparagine | 300 ± 33 | + | + |
l-Aspartic acid | 231 ± 27 | + | + |
l-Proline | 68 ± 11 | + | + |
l-Serine | 62 ± 21 | + | + |
l-Cysteinee | 1,564 ± 90 | + | − |
C. jejuni strains were assayed for respiration induced by carbon substrates present in GN2 Biolog plates (Biolog, Inc., Hayward, Calif.). The data are presented as the averages ± standard errors of the means of the normalized optical densities for 38 strains of C. jejuni. These strains included isolates from retail chicken liver and carcass samples (n = 14), human clinical isolates representing different heat-labile (Lior; n = 8) and heat-stable (Penner: n = 6) serotypes, and one calf isolate. Each strain was tested at least twice.
+ or − indicates whether the compound was detected in soluble root exudates (12, 27) or leaf exudates (13, 33).
Present in plant cell walls (47).
NR, not reported to be present.
l-Cysteine was tested separately as described in Material and Methods.