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. 2013 Apr;79(8):2670–2681. doi: 10.1128/AEM.03705-12

Fig 4.

Fig 4

(a to d) Depth distribution of chlorophyll (solid line), PAR (crosses), density (closed circles), and the concentration (mean ± standard error, n = 3) of Labrenzia-like nosZ mRNA (bars; *, not detected) at stations 1 (a) and 2 (c). The corresponding depth distributions of nitrate (closed circles) and nitrite (×5, open circles) concentrations at stations 1 (b) and 2 (d) are shown in the right-hand panels. The additional dotted line shown in panel d is the oxygen saturation profile for station 2. (e) Electrophoretogram of nosZ RT-PCR products from the Arabian Sea isolate 4N grown in denitrification medium under an aerobic atmosphere (t0) and following transfer to suboxic conditions for 30 min (t30). Equal quantities of total RNA were used for the reverse transcriptase (+RT) reactions. The absence of contaminating DNA was verified in parallel reactions in which the enzyme was omitted (−RT). The mean concentration (n = 3) of the nosZ PCR product at t30 determined by QPCR was 4.23-fold that at t0. The lower band in each lane is a mixture of QPCR primers and the fluorescein-labeled nosZ probe.