initiates as far as a threshold concentration is surpassed manifold physiological reactions on N 2 -fixation. Organic N and ammonium oxidised to NO 3 -means oxygen depletion. Plants suffering under O 2 or infection stress start to excrete ethylene (C 2 H 4 ). C 2 H 4 widens the root intercellulars that O 2 -respiration will continue. Now microbes may more easily enter the plant interior by transforming the reached methionine into C 2 H 4 . Surplus nitrate and C 2 H 4 inhibit nodulation of leguminous plants. Excess NO 3 -in the nodulesphere could be diminished by N 2 -fixing bacteria which in addition can denitrify or ammonify nitrate. Consequently, it was asked whether C 2 H 4 interferes with the potential of N 2 -fixing bacteria to reduce nitrate. The groundnut-nodule isolate TNAU 14, from which it was known that it denitrifies and ammonifies nitrate, served as inoculum of a KNO 3 -mannitol-medium that was incubated under N 2 -, 1% (v/v) N 2 -C 2 H 4 -, and 1% (v/v) N 2 -C 2 H 2 -atmosphere in the laboratory. C 2 H 2 was included into the experiments because it is frequently used to quantify N 2 -fixing potentials (acetylene reduction array, ARA). Gene-16S rDNA-sequencing and physiological tests revealed a high affiliation of strain TNAU 14 to Rhizobium radiobacter and Rhizobium tumefaciens. Strain TNAU 14 released N 2 O into the bottle headspace in all treatments, surprisingly significantly less in presence of C 2 H 2 . Nitrate-ammonification was even completely blocked by C 2 H 2 . C 2 H 4 , in contrast , rather stimulated growth, denitrification, and nitrate-ammonification of strain TNAU 14 which consumed the released NH 4 + during continuing incubation.