TY - JOUR
T1 - Poly-γ-glutamic acid production of Bacillus subtilis (natto) in the absence of DegQ
T2 - A gain-of-function mutation in yabJ gene
AU - Hong, Le Thi Thu
AU - Hachiya, Tsuyoshi
AU - Hase, Sumitaka
AU - Shiwa, Yuh
AU - Yoshikawa, Hirofumi
AU - Sakakibara, Yasubumi
AU - Nguyen, Sy Le Thanh
AU - Kimura, Keitarou
N1 - Funding Information:
L.T.T.H. acknowledges the United Nations University and the UNU-Kirin fellowship program. This work was partly supported by funds from the Ministry of Agriculture, Forestry, and Fisheries , Society for the Promotion of Science of Japan , and the MEXT-supported Program for Strategic Research Foundation at Private Universities , 2013–2017 ( S1311017 ). We are grateful to all members of the applied microbiology laboratory of NFRI. The authors have declared that there is no conflict of interest. K.K. designed the scheme of study. L.T.T.H., K.K., and N.S.L.T. performed genetic and biochemical experiments. T.H., S.H., Y.S., H.Y., and Y.S. carried out the whole genome sequencing and data processing. The manuscript was written by K.K. and L.T.T.H.
Funding Information:
L.T.T.H. acknowledges the United Nations University and the UNU-Kirin fellowship program. This work was partly supported by funds from the Ministry of Agriculture, Forestry, and Fisheries, Society for the Promotion of Science of Japan, and the MEXT-supported Program for Strategic Research Foundation at Private Universities, 2013?2017 (S1311017). We are grateful to all members of the applied microbiology laboratory of NFRI. The authors have declared that there is no conflict of interest. K.K. designed the scheme of study. L.T.T.H. K.K. and N.S.L.T. performed genetic and biochemical experiments. T.H. S.H. Y.S. H.Y. and Y.S. carried out the whole genome sequencing and data processing. The manuscript was written by K.K. and L.T.T.H.
Publisher Copyright:
© 2019 The Society for Biotechnology, Japan
PY - 2019/12
Y1 - 2019/12
N2 - Poly-γ-glutamic acid (γPGA) production by Bacillus subtilis is regulated by the quorum sensing system where DegQ transmits the cell density signal to a DNA-binding protein DegU. A mutation suppressing the γPGA-negative phenotype of degQ gene knock-out mutant (ΔdegQ) was identified through whole genome sequencing. The mutation conferred an amino acid substitution of Ser103 to phenylalanine (S103F) in yabJ that belongs to the highly conserved YjgF/YER057c/UK114 family. Genetic experiments including LacZ-fusion assay of γPGA synthetic operon confirmed that the suppressor mutation (yabJS103F) was responsible for the recovery of γPGA production. The yabJ itself was not essential for the γPGA production and the mutant allele enabled γPGA production of the ΔdegQ strain even in the presence of wild type yabJ. Thus, yabJS103F was a dominant positive allele. degU-lacZ fusion gene was hyper-expressed in cells carrying the yabJS103F, but disruption of yabJ did not affect the transcription level of the degU-lacZ. These observations suggested that YabJ acquired a function to stimulate expression of degU by the S103F mutation which is involved in the regulation of γPGA synthesis.
AB - Poly-γ-glutamic acid (γPGA) production by Bacillus subtilis is regulated by the quorum sensing system where DegQ transmits the cell density signal to a DNA-binding protein DegU. A mutation suppressing the γPGA-negative phenotype of degQ gene knock-out mutant (ΔdegQ) was identified through whole genome sequencing. The mutation conferred an amino acid substitution of Ser103 to phenylalanine (S103F) in yabJ that belongs to the highly conserved YjgF/YER057c/UK114 family. Genetic experiments including LacZ-fusion assay of γPGA synthetic operon confirmed that the suppressor mutation (yabJS103F) was responsible for the recovery of γPGA production. The yabJ itself was not essential for the γPGA production and the mutant allele enabled γPGA production of the ΔdegQ strain even in the presence of wild type yabJ. Thus, yabJS103F was a dominant positive allele. degU-lacZ fusion gene was hyper-expressed in cells carrying the yabJS103F, but disruption of yabJ did not affect the transcription level of the degU-lacZ. These observations suggested that YabJ acquired a function to stimulate expression of degU by the S103F mutation which is involved in the regulation of γPGA synthesis.
KW - Bacillus subtilis
KW - DegQ
KW - Gain-of-function mutation
KW - Poly-γ-glutamic acid
KW - YabJ
KW - YjgF/YER057c/UK114
UR - http://www.scopus.com/inward/record.url?scp=85068047220&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068047220&partnerID=8YFLogxK
U2 - 10.1016/j.jbiosc.2019.05.014
DO - 10.1016/j.jbiosc.2019.05.014
M3 - Article
C2 - 31272833
AN - SCOPUS:85068047220
SN - 1389-1723
VL - 128
SP - 690
EP - 696
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 6
ER -