TY - JOUR
T1 - Quantitative measurement of damage caused by 1064-nm wavelength optical trapping of Escherichia coli cells using on-chip single cell cultivation system
AU - Ayano, Satoru
AU - Wakamoto, Yuichi
AU - Yamashita, Shinobu
AU - Yasuda, Kenji
N1 - Funding Information:
We thank Dr. I. Inoue and Mr. K. Matsumura for their valuable discussion. This work was supported by Grants-in-Aid for Science Research from The Ministry of Education, Culture, Sports and Technology of Japan, and by the Japan Science and Technology Agency (JST).
PY - 2006/11/24
Y1 - 2006/11/24
N2 - We quantitatively examined the possible damage to the growth and cell division ability of Escherichia coli caused by 1064-nm optical trapping. Using the synchronous behavior of two sister E. coli cells, the growth and interdivision times between those two cells, one of which was trapped by optical tweezers, the other was not irradiated, were compared using an on-chip single cell cultivation system. Cell growth stopped during the optical trapping period, even with the smallest irradiated power on the trapped cells. Moreover, the damage to the cell's growth and interdivision period was proportional to the total irradiated energy (work) on the cell, i.e., irradiation time multiplied by irradiation power. The division ability was more easily affected by a smaller energy, 0.36 J, which was 30% smaller than the energy that adversely affected growth, 0.54 J. The results indicate that the damage caused by optical trapping can be estimated from the total energy applied to cells, and furthermore, that the use of optical trapping for manipulating cells might cause damage to cell division and growth mechanisms, even at wavelengths under 1064 nm, if the total irradiation energy is excessive.
AB - We quantitatively examined the possible damage to the growth and cell division ability of Escherichia coli caused by 1064-nm optical trapping. Using the synchronous behavior of two sister E. coli cells, the growth and interdivision times between those two cells, one of which was trapped by optical tweezers, the other was not irradiated, were compared using an on-chip single cell cultivation system. Cell growth stopped during the optical trapping period, even with the smallest irradiated power on the trapped cells. Moreover, the damage to the cell's growth and interdivision period was proportional to the total irradiated energy (work) on the cell, i.e., irradiation time multiplied by irradiation power. The division ability was more easily affected by a smaller energy, 0.36 J, which was 30% smaller than the energy that adversely affected growth, 0.54 J. The results indicate that the damage caused by optical trapping can be estimated from the total energy applied to cells, and furthermore, that the use of optical trapping for manipulating cells might cause damage to cell division and growth mechanisms, even at wavelengths under 1064 nm, if the total irradiation energy is excessive.
KW - 1064-nm wavelength laser
KW - Cell division
KW - Cell growth
KW - Damage
KW - Escherichia coli
KW - Hyperbolic curve of damage
KW - Isolated cultivation
KW - On-chip single-cell cultivation
KW - Optical tweezers
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U2 - 10.1016/j.bbrc.2006.09.115
DO - 10.1016/j.bbrc.2006.09.115
M3 - Article
C2 - 17027921
AN - SCOPUS:33749606327
SN - 0006-291X
VL - 350
SP - 678
EP - 684
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -