Abstract: The present invention discloses a strain of Pseudomonas aeruginosa with monomethylamine degradability and the application thereof. This strain, named Pseudomonas aeruginosa GDUTAN1, was deposited on May 24, 2017 in the China Center for Type Culture Collection in Wuhan University, Wuhan City, Hubei Province with a deposit number of CCTCC NO.: M 2017283. This Pseudomonas aeruginosa GDUTAN1 was Gram-negative and rod-like, and round, green and opaque in the colony morphology, having a diameter of 1-2 mm. The Pseudomonas aeruginosa GDUTAN1 of the present invention can be applied to environmental remediation, degrading monomethylamine in the environment at a high degradation efficiency. When it degrades monomethylamine for 96 h at a substrate concentration of 50-140 mg/L, the degradation efficiency can reach more than 99%.

Abstract: The present invention discloses a strain of Achromobacter xylosoxidans with monomethylamine degradability and the application thereof. This strain, named Achromobacter xylosoxidans GDUTAN5, was deposited on May 24, 2017 in the China Center for Type Culture Collection in Wuhan University (No. 299 Bayi Road, Wuchang District, Wuhan City, Hubei Province) with a deposit number of CCTCC NO: M 2017285. This Achromobacter xylosoxidans GDUTAN5 was Gram-negative and rod-shaped, and the colony appeared to be round, light yellow, opaque and smooth, having a diameter of 1-2 mm. The Achromobacter xylosoxidans GDUTAN5 of the present invention can be applied to environmental restoration, degrading monomethylamine in the environment at a high degradation efficiency. When it degraded monomethylamine for 96 h at a substrate concentration of 5 mg/L, the degradation efficiency could reach 92.3%.

Abstract: The present invention discloses a strain of Lysinibacillus fusiformis with methylamine degradability and the application thereof. This strain, named Lysinibacillus fusiformis GDUTAN2, was deposited on May 24, 2017 in the China Center for Type Culture Collection in Wuhan University, Wuhan City, Hubei Province with a deposit number of CCTCC NO. M 2017284. This Lysinibacillus fusiformis GDUTAN2 was Grain-positive and rod-shaped, and the colony appeared to be round, white and transparent, having a diameter of 1-2 mm. The Lysinibacillus fusiformis GDUTAN2 of the present invention can be applied to environmental restoration, degrading methylamine in the environment at a high degradation efficiency. When it degraded methylamine for 96 h at a substrate concentration of 130 mg/L, the degradation efficiency could reach 32.8%.

Abstract: The present invention discloses a strain of Lysinibacillus fusiformis with methylamine degradability and the application thereof. This strain, named Lysinibacillus fusiformis GDUTAN2, was deposited on May 24, 2017 in the China Center for Type Culture Collection in Wuhan University, Wuhan City, Hubei Province with a deposit number of CCTCC NO. M 2017284. This Lysinibacillus fusiformis GDUTAN2 was Grain-positive and rod-shaped, and the colony appeared to be round, white and transparent, having a diameter of 1-2 mm. The Lysinibacillus fusiformis GDUTAN2 of the present invention can be applied to environmental restoration, degrading methylamine in the environment at a high degradation effective. When it degraded methylamine for 96 h at a substrate concentration of 130 mg/L, the degradation could reach 32.8%.

Abstract: The present invention discloses a strain of Pseudomonas aeruginosa with monomethylamine degradability and the application thereof. This strain, named Pseudomonas aeruginosa GDUTAN1, was deposited on May 24, 2017 in the China Center for Type Culture Collection in Wuhan University, Wuhan City, Hubei Province with a deposit number of CCTCC NO.: M 2017283. This Pseudomonas aeruginosa GDUTAN1 was Gram-negative and rod-like, and round, green and opaque in the colony morphology, having a diameter of 1-2 mm. The Pseudomonas aeruginosa GDUTAN1 of the present invention can be applied to environmental remediation, degrading monomethylamine in the environment at a high degradation efficiency. When it degrades monomethylamine for 96 h at a substrate concentration of 50-140 mg/L, the degradation efficiency can reach more than 99%.