Biological laser printing of genetically modified Escherichia coli for biosensor applications

被引:40
作者
Barron, JA
Rosen, R
Jones-Meehan, J
Spargo, BJ
Belkin, S
Ringeisen, BR
机构
[1] USN, Res Lab, Div Chem, Biol Chem Sect,Chem Dynam & Diagnost Branch, Washington, DC 20375 USA
[2] Hebrew Univ Jerusalem, Fredy & Nadine Herrmann Grad Sch Appl Sci, IL-91904 Jerusalem, Israel
关键词
biological laser printing (BioLp (TM)); whole-cell biosensors; bacteria-based biosensors;
D O I
10.1016/j.bios.2004.01.011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
One of the primary requirements of cell- or tissue-based sensors is the placement of cells and cellular material at or near the sensing elements of the device. The ability to achieve precise, reproducible and rapid placement of cells is the focus of this study. We have developed a technique, biological laser printing or BioLP(TM), which satisfies these requirements and has advantages over current technologies. BioLp(TM) is capable of rapidly depositing patterns of active biomolecules and living cells onto a variety of material surfaces. Unlike ink jet or manual spotting techniques, this process delivers small volume (nl to fl) aliquots of biomaterials without the use of an orifice, thus eliminating potential clogging issues and enabling diverse classes of biomaterials to be deposited. This report describes the use of this laser-based printing method to transfer genetically-modified-bacteria capable of responding to various chemical stressors; onto agar-coated slides and into microtiter plates. The BioLp(TM) technology enables smaller spot sizes, increased resolution, and improved reproducibility compared to related technologies. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:246 / 252
页数:7
相关论文
共 24 条
[21]   Functional genomics:: Expression analysis of Escherichia coli growing on minimal and rich media [J].
Tao, H ;
Bausch, C ;
Richmond, C ;
Blattner, FR ;
Conway, T .
JOURNAL OF BACTERIOLOGY, 1999, 181 (20) :6425-6440
[22]   Detection of DNA damage by use of Escherichia coli carrying recA'-lux, uvrA'-lux, or alkA'-lux reporter plasmids [J].
Vollmer, AC ;
Belkin, S ;
Smulski, DR ;
VanDyk, TK ;
LaRossa, RA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (07) :2566-2571
[23]   Cell and organ printing 1: Protein and cell printers [J].
Wilson, WC ;
Boland, T .
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY, 2003, 272A (02) :491-496
[24]   Laser transfer of biomaterials:: Matrix-assisted pulsed laser evaporation (MAPLE) and MAPLE Direct Write [J].
Wu, PK ;
Ringeisen, BR ;
Krizman, DB ;
Frondoza, CG ;
Brooks, M ;
Bubb, DM ;
Auyeung, RCY ;
Piqué, A ;
Spargo, B ;
McGill, RA ;
Chrisey, DB .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2003, 74 (04) :2546-2557