Transcriptional and metabolic response against hydroxyethane-(1,1-bisphosphonic acid) on bacterial denitrification by a halophilic Pannonibacter sp. strain DN

• Published in: Chemosphere (Oxford) 2020-08, Vol.252, p.126478-126478, Article 126478
• Main Authors: Koju, Rashmi, Miao, Shiyu, Liang, Bin, Joshi, Dev Raj, Bai, Yaohui, Liu, Ruiping, Qu, Juihui
• Format: Article
• Language: English
• Subjects: Denitrification; Hydroxyethane-(1,1-bisphosphonic acid); Membrane potential; Pannonibacter sp. DN; Transcriptional profiling
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2020.126478

Biological denitrification is an environmentally sound pathway for the elimination of nitrogen pollution in wastewater treatment. Extreme environmental conditions, such as the co-existence of toxic organic pollutants, can affect biological denitrification. However, the potential underlying mechanism remains largely unexplored. Herein, the effect of a model pollutant, hydroxyethane-(1,1-bisphosphonic acid) (HEDP), a widely applied and consumed bisphosphonate, on microbial denitrification was investigated by exploring the metabolic and transcriptional responses of an isolated denitrifier, Pannonibacter sp. strain DN. Results showed that nitrate removal efficiency decreased from 85% to 50% with an increase in HEDP concentration from 0 to 3.5 mM, leading to nitrite accumulation of 204 mg L−1 in 3.5 mM HEDP. This result was due to the lower bacterial population count and reduction in the live cell percentage. Further investigation revealed that HEDP caused a decrease in membrane potential from 0.080 ± 0.005 to 0.020 ± 0.002 with the increase in HEDP from 0 to 3.5 mM. This hindered electron transfer, which is required for nitrate transformation into nitrogen gas. Moreover, transcriptional profiling indicated that HEDP enhanced the genes involved in ROS (O2−) scavenging, thus protecting cells against oxidative stress damage. However, the suppression of genes responsible for the production of NADH/FADH2 in tricarboxylic acid cycle (TCA), NADH catalyzation (NADH dehydrogenase) in (electron transport chain) ETC system and denitrifying genes, especially nor and nir, in response to 2.5 mM HEDP were identified as the key factor inhibiting transfer of electron from TCA cycle to denitrifying enzymes through ETC system. [Display omitted] •Effect of HEDP on denitrification by Pannonibacter sp. DN was investigated.•Inhibited cell growth affecting denitrification through the accumulation of nitrite.•Membrane potential collapse and decrease of reductase activity were observed.•Genes associated to TCA cycle, ETC system and denitrification were down-regulated.