24-10-2019 дата публикации
Номер: US20190322995A1
Автор:
Jiyin MA,
Tingyi WEN,
Shuwen LIU,
Yong LIANG,
Daihuan LI,
Yun ZHANG,
Xiuling SHANG,
Chunguang ZHAO,
Xiaowei GUO,
Gang MENG,
MA JIYIN,
WEN TINGYI,
LIU SHUWEN,
LIANG YONG,
LI DAIHUAN,
ZHANG YUN,
SHANG XIULING,
ZHAO CHUNGUANG,
GUO XIAOWEI,
MENG GANG,
MA, Jiyin,
WEN, Tingyi,
LIU, Shuwen,
LIANG, Yong,
LI, Daihuan,
ZHANG, Yun,
SHANG, Xiuling,
ZHAO, Chunguang,
GUO, Xiaowei,
MENG, Gang
A method for fermentation-production of a pentanediamine, comprising: culturing a cell expressing a lysine decarboxylase to obtain a whole cell fermentation broth comprising a pentanediamine; and extracting the pentanediamine from the whole cell fermentation broth, and striping the whole cell fermentation broth of carbon dioxide contained therein before adding a strong base. The method greatly increases a production volume of the pentanediamine. 1. A method for preparing 1 ,5-pentanediamine by fermentation , comprising:(1) culturing a cell expressing a lysine decarboxylase to obtain a fermentation broth comprising 1, 5-pentanediamine;(21) separating the liquid from the fermentation broth;(22) removing carbon dioxide from the liquid obtained in the step (21), and then adding a base for treatment;(23) extracting a composition containing 1,5-pentanediamine from the treatment liquid obtained in the step (22).2. The method according to claim 1 , wherein in step (1) claim 1 , the cell is a cell overexpressing lysine decarboxylase.3. The method according to claim 1 , wherein in step (1) claim 1 , the cell is a cell with enhanced lysine decarboxylase gene expression.4. The method according to claim 1 , wherein in step (1) claim 1 , the cell is a cell whose expression is enhanced by replacing the promoter of the lysine decarboxylase gene with a strong promoter.5. The method according to claim 1 , wherein in step (1) claim 1 , the cell is a cell whose expression is enhanced by replacing the promoter of the lysine decarboxylase gene with T7 promoter.6. The method according to claim 1 , wherein in step (1) claim 1 , the cell is a bacterial cell.7E. coli. The method according to claim 1 , wherein in step (1) claim 1 , the cell is an cell.8E. coli. The method according to claim 1 , wherein in step (1) claim 1 , the cell is BL21 (DE3).9. The method according to claim 1 , wherein in step (1) claim 1 , no acidic pH regulator is added to the culture claim 1 , and the cells themselves ...
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