TY - JOUR
T1 - Stabilization of recombinant bioluminescent bacteria for biosensor applications
AU - Pedahzur, Rami
AU - Rosen, R.
AU - Belkin, S.
PY - 2004
Y1 - 2004
N2 - The effects of growth media, drying protocols, and storage conditions on the long-term survival and activity of Escherichia coli, which harbors genetic fusions of inducer-responsive promoters to bacterial luminescence (lux) genes, were evaluated. Bacteria were grown in a regular of high-salinity (0.5 M NaCl) complex medium (Luria-Bertani, LB) or minimal medium (M-9), freeze-dried or dried by vacuum under ambient temperatures, and stored at -20°C of 37°C. The survival rates of vacuum-dried and freeze-dried bacteria grown in LB ranged from 1% to 2% and 19% to 20%, respectively, and were not as affected by medium salinity. Survival rates of vacuum-dried and freeze-dried bacteria grown in M-9 ranged from 22% to 75% and 45% to 63%, respectively. Here, however, high salinity promoted survival of vacuum-dried bacteria but negatively affected the survival of freeze-dried bacteria. Survival rates of vacuum-dried bacteria stored at 37°C were substantially higher than those of freeze-dried bacteria and were maximal with high-salinity M-9-grown bacteria achieving 37% and 4.7% after 10 and 35 days, respectively. Bioreporter activity was typically correlated to survival but was affected by growth media composition and drying protocols. Interestingly, growth in high-salinity M-9 medium, which typically promoted high survival rates and improved storage stability, caused a substantial decrease in activity of tested bioreporter strains. Our results demonstrate the need to further optimize growth conditions and drying protocols for improved short- and long-term stability of our dried bioreporter bacteria, especially upon storage under ambient conditions.
AB - The effects of growth media, drying protocols, and storage conditions on the long-term survival and activity of Escherichia coli, which harbors genetic fusions of inducer-responsive promoters to bacterial luminescence (lux) genes, were evaluated. Bacteria were grown in a regular of high-salinity (0.5 M NaCl) complex medium (Luria-Bertani, LB) or minimal medium (M-9), freeze-dried or dried by vacuum under ambient temperatures, and stored at -20°C of 37°C. The survival rates of vacuum-dried and freeze-dried bacteria grown in LB ranged from 1% to 2% and 19% to 20%, respectively, and were not as affected by medium salinity. Survival rates of vacuum-dried and freeze-dried bacteria grown in M-9 ranged from 22% to 75% and 45% to 63%, respectively. Here, however, high salinity promoted survival of vacuum-dried bacteria but negatively affected the survival of freeze-dried bacteria. Survival rates of vacuum-dried bacteria stored at 37°C were substantially higher than those of freeze-dried bacteria and were maximal with high-salinity M-9-grown bacteria achieving 37% and 4.7% after 10 and 35 days, respectively. Bioreporter activity was typically correlated to survival but was affected by growth media composition and drying protocols. Interestingly, growth in high-salinity M-9 medium, which typically promoted high survival rates and improved storage stability, caused a substantial decrease in activity of tested bioreporter strains. Our results demonstrate the need to further optimize growth conditions and drying protocols for improved short- and long-term stability of our dried bioreporter bacteria, especially upon storage under ambient conditions.
UR - http://www.scopus.com/inward/record.url?scp=12344329593&partnerID=8YFLogxK
U2 - 10.1089/cpt.2004.2.260
DO - 10.1089/cpt.2004.2.260
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AN - SCOPUS:12344329593
SN - 1538-344X
VL - 2
SP - 260
EP - 269
JO - Cell Preservation Technology
JF - Cell Preservation Technology
IS - 4
ER -