TY - JOUR
T1 - Efficient production of poly(γ-glutamic acid) by newly isolated Bacillus subtilis NX-2
AU - Xu, Hong
AU - Jiang, Min
AU - Li, Hui
AU - Lu, Dingqiang
AU - Ouyang, Pingkai
PY - 2005/2
Y1 - 2005/2
N2 - A bacterium with high poly(γ-glutamic acid) (γ-PGA) productivity was isolated from soil. The bacterial strain NX-2 was identified taxonomically as Bacillus subtilis with the exception that it could not assimilate citric acid. The production of γ-PGA was investigated. Exogenous glutamic acid and additional carbon source was necessary for the production of γ-PGA. The suitable carbon sources were glucose, sucrose, maltose, starch and glycerol. However, γ-PGA could not be produced when citric acid was used as carbon sources, which is different from the other bacteria reported before. The amount of γ-PGA increased upon addition of glutamic acid to the medium. When 70 g/l of L-glutamic acid was added to the medium, the highest γ-PGA concentration of 41 g/l was obtained. But the apparent conversion rate to L-glutamic acid substrate was relatively low, only 58% in this case. The amount of γ-PGA reached 30.2 g/l in the presence of 30 g/l L-glutamic acid after the short incubation time of 24 h, resulting in the high apparent conversion rate of 101% and high productivity of 1.26 g/l/h. The total amount of glutamic acid including that accumulated in γ-PGA and residual glutamic acid in broth was much more than the glutamic acid supplied to the medium. The yield of γ-PGA also exceeded the amount of glutamic acid came from glucose conversion. This showed that the glutamic acid units in γ-PGA not only came from the glutamic acid added to the medium but also from glucose through the de novo pathway of glutamic acid synthesis.
AB - A bacterium with high poly(γ-glutamic acid) (γ-PGA) productivity was isolated from soil. The bacterial strain NX-2 was identified taxonomically as Bacillus subtilis with the exception that it could not assimilate citric acid. The production of γ-PGA was investigated. Exogenous glutamic acid and additional carbon source was necessary for the production of γ-PGA. The suitable carbon sources were glucose, sucrose, maltose, starch and glycerol. However, γ-PGA could not be produced when citric acid was used as carbon sources, which is different from the other bacteria reported before. The amount of γ-PGA increased upon addition of glutamic acid to the medium. When 70 g/l of L-glutamic acid was added to the medium, the highest γ-PGA concentration of 41 g/l was obtained. But the apparent conversion rate to L-glutamic acid substrate was relatively low, only 58% in this case. The amount of γ-PGA reached 30.2 g/l in the presence of 30 g/l L-glutamic acid after the short incubation time of 24 h, resulting in the high apparent conversion rate of 101% and high productivity of 1.26 g/l/h. The total amount of glutamic acid including that accumulated in γ-PGA and residual glutamic acid in broth was much more than the glutamic acid supplied to the medium. The yield of γ-PGA also exceeded the amount of glutamic acid came from glucose conversion. This showed that the glutamic acid units in γ-PGA not only came from the glutamic acid added to the medium but also from glucose through the de novo pathway of glutamic acid synthesis.
KW - Bacillus subtilis
KW - Glucose
KW - Glutamic acid
KW - Poly(γ-glutamic acid)
KW - Screening
UR - http://www.scopus.com/inward/record.url?scp=7444226967&partnerID=8YFLogxK
U2 - 10.1016/j.procbio.2003.09.025
DO - 10.1016/j.procbio.2003.09.025
M3 - 文章
AN - SCOPUS:7444226967
SN - 1359-5113
VL - 40
SP - 519
EP - 523
JO - Process Biochemistry
JF - Process Biochemistry
IS - 2
ER -