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Comparative study of aerobic and nitrate respiration in Pseudomonas stutzeri

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Title Comparative study of aerobic and nitrate respiration in Pseudomonas stutzeri
Names Mayeux, Jerry Vincent (creator)
Gilmour, Campbell M. (advisor)
Date Issued 1964-12-12 (iso8601)
Note Graduation date: 1965
Abstract Some forms of bacterial respiration do not involve molecular
oxygen but instead utilize other hydrogen acceptors for oxidation
of the substrate. Various organic and inorganic acceptors may be
used. In the present study, the inorganic radicals, nitrate and
nitrite, were investigated. Preliminary evidence indicated that
nitrate and oxygen are able to compete effectively as acceptors of
hydrogen in respiration. It is the purpose of this dissertation to
extend this observation with the hope that the degree of competition
may be elucidated and information obtained regarding the
conditions under which nitrate and nitrite can most effectively
compete with oxygen.
A strain of Pseudomonas stutzeri was used throughout the study.
Experiments were conducted with the closed electrolytic respirometer
flasks which could be flushed with helium gas for anaerobic studies
or with 20% oxygen in helium for aerobic studies. The vessels
containing a magnetic bar were set on magnetic stirrers to obtain
maximum aeration of the medium. Samples of the respirometer atmosphere
were assayed with a Beckman GC-2 gas chromatograph. Analyses
for CO₂, NO₃⁻, NO₂⁻ and fermentation products were performed by
conventional procedures. Dissolved oxygen was measured with a
Precision Scientific Oxygen Analyzer.
P. stutzeri has a definite requirement for some component supplied
by yeast extract. No denitrifying activity is noted in the
absence of yeast extract. Neither nitrate nor nitrite can be assimilated
by the cell although either can be used as the sole
hydrogen acceptor in respiration. Data are presented for nitrite
respiration which indicate that this respiratory system may be
similar to that of the oxygen system insofar as the atoms of oxygen
required for oxidation of the carbon substrate. The nitrate respiring
system seems to be less efficient, particularly when using the
nitrate to nitrite reduction step. An [0]/C ratio of 2.0 is obtained
for nitrite whereas the mean ratio for nitrate is 2.5.
Excretion of fermentation products appears to be due to a sluggish
acceptor system or to the complete absence of acceptor. Pyruvate,
acetate and succinate are metabolized without difficulty.
The cell density greatly influenced the dissolved oxygen content
of the agitated medium. This in turn determined the rate at
which nitrate and nitrite could be reduced in the aerobic system.
Too dense a cell suspension leads to "aerobic denitrification"
because the conditions of the medium per se were not aerobic.
Attempts to correlate dissolved oxygen with "aerobic denitrification showed that at a D.O. as low as 0.9 ppm no denitrification occurred.
With cell optical densities of 0.5 to 1.0 (0.25 to 0.5 mg dry wt.)
very active stirring of the medium was required to maintain the D.O.
above 1.0 ppm for a 24 hour period. Although no N₂ gas was produced,
nitrate was reduced to nitrite.
The reduction of oxygen uptake by high nitrate concentrations
was first noted at 4000 ppm NO₃⁻-N (0.28 molar) and increased with
increase of nitrate. A solution of 8000 ppm (0.57 molar) gave a
lag lasting about 3 hours. Solutions of other salts at 0.57 molar
(NH₄C1, KC1, KNO₃, NH₄NO₃ and K₂SO₄) also caused a reduction in
oxygen uptake. The effect was greatest with the nitrate salts.
A 0.57 M solution of (NH₄)₂HPO₄ had no apparent effect on oxygen
consumption.
Solutions (0.50 M) of KC1, K₂SO₄ and KNO₃ exerted no apparent
influence on the reduction of nitrate to nitrite, but the further
reduction of nitrite to N₂ (nitrite respiration) was almost completely
inhibited during the 30 hour test period. This was true
for both nitrite accumulated from nitrate and for nitrite added in
the absence of nitrate.
Genre Thesis/Dissertation
Topic Pseudomonadaceae
Identifier http://hdl.handle.net/1957/49045

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