1. Academic Validation
  2. Identification and characterization of Nornicotine degrading strain Arthrobacter sp. NOR5

Identification and characterization of Nornicotine degrading strain Arthrobacter sp. NOR5

  • Sci Total Environ. 2021 Apr 10;764:142894. doi: 10.1016/j.scitotenv.2020.142894.
Rabia Najme 1 Shulin Zhuang 2 Jiguo Qiu 3 Zhenmei Lu 4
Affiliations

Affiliations

  • 1 MOE Laboratory of Biosystem Homeostasis and Protection, College of Life Sciences, Zhejiang University, Hangzhou 310058, China; College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China.
  • 2 College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China.
  • 3 Key Laboratory of Agricultural Environmental Microbiology, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, China. Electronic address: qiujiguo@njau.edu.cn.
  • 4 MOE Laboratory of Biosystem Homeostasis and Protection, College of Life Sciences, Zhejiang University, Hangzhou 310058, China. Electronic address: lzhenmei@zju.edu.cn.
Abstract

Nornicotine, the primary nicotine metabolite that is formed through demethylation of nicotine in the genus Nicotiana tabacum L. Nornicotine is not only a precursor of tobacco-specific nitrosamine N-nitrosonornicotine but also have detrimental effects to human health. Till now, information on the biotransformation of nornicotine is limited. Herein, we identified and characterized a bacterium Arthrobacter sp. strain NOR5, utilized nornicotine as the sole of carbon and energy source, and degraded 500 mg/L nornicotine completely within 60 h under the optimum conditions of pH 7.0 and 30 °C. In this study, we not only identified previously reported intermediate metabolites such as 6-OH-nornicotine, 6-OH-mysomine, 6-OH-pseudooxy-nornicotine (6HPONor) but also identified a new intermediate metabolite 2,6-di-OH-pseudooxy-nornicotine (2,6DHPONor) by UV spectroscopy and liquid chromatography coupled with time of flight mass spectrometry. About half of 6HPONor could be transformed into 2,6DHPONor that was identified as a novel catabolic intermediate of nornicotine. By the addition of an electron acceptor 2,6-dichlorophenolindophenol (DCIP), the cell-free extract exhibited inducible 6HPONor dehydrogenase activity at 179 ± 60 mU/mg that could convert 6HPONor to 2,6DHPONor. Our study demonstrated that Arthrobacter sp. strain NOR5 has a high potential to degrade the nornicotine completely.

Keywords

2,6-Di-OH-hydroxy-pseudooxy-nornicotine; Arthrobacter sp. NOR5; Biodegradation; Dehydrogenase; Intermediates; Nornicotine.

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