Tian, Wei, The biological
metabolism of nitrate and nitrite in Pseudomonas fluorescens K27 amended
with tellurium. Master of Science (Chemistry), December 2004, Sam Houston
State University, Huntsville, Texas, 82 pp. (pdf version
of this thesis)
The purpose of this research was to determine
the initial steps in the nitrate and nitrite metabolism of Pseudomonas fluorescens
K27, investigate tellurite influence on this reduction and whether K27 has a
nitrate assimilatory system and determine if K27 has separate nitrate and nitrite
reductase systems.
Experiments were carried out by inoculating
Pseudomonas fluorescens K27 in growth medium with or without tellurite
amendment and growing anaerobically. Samples were analyzed in regular time intervals
for cell growth using optical density, for extracellular ammonium ion concentration
using an ammonia-selective electrode, and for extracellular nitrate and nitrite
content using colorimetric or UV-VIS spectrometry.
Nitrate is a preferred terminal electron
acceptor for the anaerobic growth of K27 in tryptic soy broth medium. Nitrite
acts as both a terminal electron acceptor and toxic reagent: low level nitrite
supports the anaerobic growth of K27; high level nitrite inhibits the anaerobic
growth of K27.
Nitrate and nitrite were reduced concomitantly
in the anaerobic conditions studied; nitrate reduction rate was faster than
nitrite reduction rate as measured by the disappearance of these anions in growing
cultures. Part of the newly-formed nitrite bacterially produced was further
reduced; the other unreduced nitrite accumulated to its highest level at the
point in time at which nitrate was used up.
Ammonium ion was produced by K27 in the minimal
medium used in other experiments with NO3- as the only
N source. At the time point that the nitrate was used up, both nitrite and ammonium
concentrations attained their highest level. After that, nitrite and ammonium
concentrations gradually decreased.
In tryptic soy broth with added nitrate amended
with tellurite, the specific growth rate of K27 was inhibited; nitrate uptake
per bacterium also was decreased. In tryptic soy broth with added nitrate and
with 0.1 mmol/L tellurite amendment, nitrate was used up in 5 days but nitrite
was at high levels after 7 days. In this same medium with 0.2 mmol/L tellurite
added, both nitrate and nitrite were not used up after 7 days.
In tellurite-amended conditions, before the
point of change at which nitrite gained its highest concentration in solution,
tellurite inhibited a little bit of the nitrate reduction and decreased nitrite
reduction a lot. Therefore newly-formed nitrite concentration was increased
faster than that in cultures without tellurite amendment. K27 apparently has
separate nitrate and nitrite reductase systems because the reduction of these
anions is carried on concomitantly no matter which anion is higher in concentration.
Nitrate is used up first even in growth media of high levels of nitrite. On
the other hand, nitrite reduction is not stopped even if the nitrate concentration
is high.