TY - JOUR
T1 - Low yield and abiotic origin of N2O formed by the complete nitrifier Nitrospira inopinata
AU - Kits, Kerim
AU - Jung, Man-Young
AU - Vierheilig, Julia
AU - Pjevac, Petra
AU - Sedlacek, Christopher J.
AU - Liu, Shurong
AU - Herbold, Craig
AU - Stein, Lisa Y.
AU - Richter, Andreas
AU - Wissel, Holger
AU - Brueggemann, Nicolas
AU - Wagner, Michael
AU - Daims, Holger
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2019/4/23
Y1 - 2019/4/23
N2 - Nitrous oxide (N2O) and nitric oxide (NO) are atmospheric trace gases that contribute to climate change and affect stratospheric and ground-level ozone concentrations. Ammonia oxidizing bacteria (AOB) and archaea (AOA) are key players in the nitrogen cycle and major producers of N2O and NO globally. However, nothing is known about N2O and NO production by the recently discovered and widely distributed complete ammonia oxidizers (comammox). Here, we show that the comammox bacterium Nitrospira inopinata is sensitive to inhibition by an NO scavenger, cannot denitrify to N2O, and emits N2O at levels that are comparable to AOA but much lower than AOB. Furthermore, we demonstrate that N2O formed by N. inopinata formed under varying oxygen regimes originates from abiotic conversion of hydroxylamine. Our findings indicate that comammox microbes may produce less N2O during nitrification than AOB.
AB - Nitrous oxide (N2O) and nitric oxide (NO) are atmospheric trace gases that contribute to climate change and affect stratospheric and ground-level ozone concentrations. Ammonia oxidizing bacteria (AOB) and archaea (AOA) are key players in the nitrogen cycle and major producers of N2O and NO globally. However, nothing is known about N2O and NO production by the recently discovered and widely distributed complete ammonia oxidizers (comammox). Here, we show that the comammox bacterium Nitrospira inopinata is sensitive to inhibition by an NO scavenger, cannot denitrify to N2O, and emits N2O at levels that are comparable to AOA but much lower than AOB. Furthermore, we demonstrate that N2O formed by N. inopinata formed under varying oxygen regimes originates from abiotic conversion of hydroxylamine. Our findings indicate that comammox microbes may produce less N2O during nitrification than AOB.
KW - NITROUS-OXIDE PRODUCTION
KW - AMMONIA-OXIDIZING ARCHAEA
KW - NITROSOMONAS-EUROPAEA
KW - NITROSOSPHAERA-VIENNENSIS
KW - COMPLETE NITRIFICATION
KW - NITRITE OXIDATION
KW - KINETIC-ANALYSIS
KW - SITE PREFERENCE
KW - DENITRIFICATION
KW - REDUCTASE
UR - http://www.scopus.com/inward/record.url?scp=85064907451&partnerID=8YFLogxK
U2 - 10.1038/s41467-019-09790-x
DO - 10.1038/s41467-019-09790-x
M3 - Article
VL - 10
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 1836
ER -