The invention provides a suspension-
cultured cell of Acer ginnala Maxim for producing
gallic acid, which is characterized in that a proper amount of
callus of Acer ginnala Maxim is inoculated in a
solid cultivation medium containing WPM+TDZ 0.002-0.01 mg / L+6-BA 0.05-0.15 mg / L for successive transfer culture for 15 to 20 days to obtain a first successive generation; a well-growing
callus is transformed into a triple WPM
liquid medium containing a large amount of elements and having a pH value of 5.8 to 6.0, in the presence of a
hormone including TDZ 0.002 to 0.010 mg / L and 6-BA 0.05 to 0.15 mg / L and 2% to 3%
sugar to obtain the
fresh weight of an inoculum size of 20 to 40 g / L; and the culture conditions comprises the temperature of 23 to 25 DEG C, the rotation speed of 110 to 130 rpm, the illumination time of 8 to 10 h / d, the illumination intensity of 1,400 to 1,700 Lx, and the culture period of the first successive generation of 7 to 15 days. The cells are collected after one period of 20 to 30 days, with the
fresh weight up to 478.2 g / L and the
dry weight up to 22.3 g / L, wherein the content of
gallic acid is up to 2.29%, the output of
gallic acid is 0.51g / L, and the gallic acid with the amount of 6.1227 g / L can be collected in one year. The invention can improve the output of suspension of gallic acid in Acer ginnala Maxim by
cell engineering method for the first time, which solves the
raw material problem for the production of gallic acid. The invention has the advantages of easy operation,
short cycle, low cost as well as greatly saved labor force and material resource,improved labor productivity and protection of environment and Acer ginnala Maxim resources.