The present invention relates to an application of bacterial in
quinoline degradation, wherein the bacterial is
Ochrobactrum sp.. According to the present invention, the optimum degradation conditions are screened, wherein the optimum bacterial H1 growth temperature through utilizing
quinoline is 30 DEG C, the initial growth pH value is 5.0, and a shaking table rotation speed is 150 r / min; the bacterial H1 meets a first order
kinetic model when the initial
quinoline concentration is within 250 mg / L, wherein a
first order reaction rate is proportional to a quinoline concentration, the reaction that the bacterial grows through utilizing quinoline belongs to the
first order reaction within the concentration range, the
specific growth rate is increased along with concentration increase, and
bacterial growth is not limited by the concentration within the concentration range; after the bacterial H1 is immobilized by using
sodium alginate, a 400 mg / L quinoline degradation rate can be 87.5% within 24h; and the crude
enzyme solution in the bacterial
cell is extracted, wherein the crude
enzyme solution can induce
catechol 1,2-
dioxygenase (C12O),
nitrogen heterocyclic ring is firstly oxidized into
quinolone during quinoline
metabolism, and then the
nitrogen heterocyclic ring is subjected to chain opening to form
benzaldehyde,
xylene, 2-
pentanone, hydroxyphenyl propionic acid and other intermediate products.