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. 2015 May 12;6:403. doi: 10.3389/fmicb.2015.00403

Table 2.

Biological properties measured in un-amended controls and gum-xanthan (GX) enriched microcosms incubated 2 days (T2d) under dark + DCMU conditions.

Parameter Units Control GX enriched
T0 T2d T0 T2d
Chl. a μg L−1 2.1±0.6 0.3±0.2 2.1±0.6 0.3±0.3
HBBa μg C L−1 47±22 60±29 47±22 86±44
HNA x108 Cell L−1 15±7.1 20±10 15±7.1 31±14
LNA x108 Cell L−1 8.3±4.6 10±4.2 8.3±4.6 11±6.3
HNA/LNA Cell/Cell 2±0.7 1.9±0.6 2±0.7 3.3±1.3
TEPb μg C L−1 160±48 384±206 1312±52 849±351
β-gluc μg C L−1 d−1 34±7.5 32±9 34±7.5 46±9
BPd μg C L−1 d−1 109±21 165±34 109±21 121±24
BCD μg C L−1 d−1 NA 359±167 NA 557±276
BGE % NA 42±22 NA 37±20
Growth ratee d−1 NA 0.15±0.1 NA 0.28±0.09

All values are the averages and their standard deviation of nine bottle incubations.

a

Bacterial abundance was converted into biomass (HBB) by a factor of 20 fg C per cell (Lee and Fuhrman, 1987).

b

TEP was converted from GX into carbon biomass using a 0.74 factor (Engel and Passow, 2001).

c

β-glucosidase activity (β-glu) was converted from MUF to carbon biomass using 72 μg C to 1 μM MUF factor (Hoppe, 1993).

d

Bacterial production was converted into carbon biomass using a conversion factor of 3.1 kg C mol−1 with an isotope dilution factor of 2.0 to calculate BP (Simon and Azam, 1989).

e

Growth rates calculated according to Equation (1).