School of Marine Science and Policy, University of Delaware Newark, DE, USA ; Delaware Biotechnology Institute, University of Delaware Newark, DE, USA.
Front Microbiol. 2013 Jul 4;4:180. doi: 10.3389/fmicb.2013.00180. eCollection 2013.
The process of nitrate reduction via nitrite controls the fate and bioavailability of mineral nitrogen within ecosystems; i.e., whether it is retained as ammonium (ammonification) or lost as nitrous oxide or dinitrogen (denitrification). Here, we present experimental evidence for a novel pathway of microbial nitrate reduction, the reverse hydroxylamine:ubiquinone reductase module (reverse-HURM) pathway. Instead of a classical ammonia-forming nitrite reductase that performs a 6 electron-transfer process, the pathway is thought to employ two catalytic redox modules operating in sequence: the reverse-HURM reducing nitrite to hydroxylamine followed by a hydroxylamine reductase that converts hydroxylamine to ammonium. Experiments were performed on Nautilia profundicola strain AmH, whose genome sequence led to the reverse-HURM pathway proposal. N. profundicola produced ammonium from nitrate, which was assimilated into biomass. Furthermore, genes encoding the catalysts of the reverse-HURM pathway were preferentially expressed during growth of N. profundicola on nitrate as an electron acceptor relative to cultures grown on polysulfide as an electron acceptor. Finally, nitrate-grown cells of N. profundicola were able to rapidly and stoichiometrically convert high concentrations of hydroxylamine to ammonium in resting cell assays. These experiments are consistent with the reverse-HURM pathway and a free hydroxylamine intermediate, but could not definitively exclude direct nitrite reduction to ammonium by the reverse-HURM with hydroxylamine as an off-pathway product. N. profundicola and related organisms are models for a new pathway of nitrate ammonification that may have global impact due to the wide distribution of these organisms in hypoxic environments and symbiotic or pathogenic associations with animal hosts.
通过亚硝酸盐进行硝酸盐还原的过程控制了生态系统中矿物氮的命运和生物可利用性;也就是说,它是作为铵(氨化作用)保留下来,还是作为一氧化二氮或氮气(反硝化作用)损失。在这里,我们提出了微生物硝酸盐还原的一种新途径,即反向羟胺:泛醌还原酶模块(reverse-HURM)途径的实验证据。该途径不采用执行 6 电子转移过程的经典氨形成亚硝酸盐还原酶,而是被认为采用两个连续作用的催化氧化还原模块:反向-HURM 将亚硝酸盐还原为羟胺,然后是羟胺还原酶将羟胺转化为铵。在 Nautilia profundicola 菌株 AmH 上进行了实验,其基因组序列导致了反向-HURM 途径的提出。N. profundicola 从硝酸盐中产生铵,然后将其同化到生物量中。此外,编码反向-HURM 途径催化剂的基因在 N. profundicola 以硝酸盐作为电子受体生长时相对于以多硫化物作为电子受体生长时优先表达。最后,N. profundicola 的硝酸盐生长细胞能够在静止细胞测定中快速且化学计量地将高浓度的羟胺转化为铵。这些实验与反向-HURM 途径和游离羟胺中间物一致,但不能明确排除羟胺作为副产物的反向-HURM 直接将亚硝酸盐还原为铵。N. profundicola 和相关生物是硝酸盐氨化作用的新途径的模型,由于这些生物在缺氧环境中的广泛分布以及与动物宿主的共生或致病关系,可能会对全球产生影响。