Construction of spores for portable bacterial whole-cell biosensing systems

被引:56
作者
Date, Arnol [1 ]
Pasini, Patrizia [1 ]
Daunert, Sylvia [1 ]
机构
[1] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
关键词
D O I
10.1021/ac701606g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Whole-cell sensing systems based on living genetically engineered bacteria are known to have high sensitivity, selectivity, and rapid response times. Although these systems have found applications in biomedical and environmental analyses, their limited shelf life and transportability still restrict their use for on-site monitoring of analytes. To that end, we have developed a new method for the long-term preservation, storage, and transport of whole-cell biosensing systems that is based on bacterial spores, a dormant form of life. Specifically, we have empl oyed spore-forming bacteria such as Bacillus subtilis and Bacillus megaterium for development of luminescent sensing systems for two model analytes, namely, arsenic and zinc. These sensing cells were converted to spores, which can then be "revived" (germinated) at a later time to generate viable and metabolically active cells. Herein, we demonstrate that these spore-based sensing systems retained their analytical performance, in terms of detection limit, dynamic range, and reproducibility, after storage at room temperature for at least 6 and 8 months, respectively, as well as after three cycles where the cells alternated between being dormant or active, i.e., sporulation-germination cycles. The ability to cycle the sensing cells between active and dormant states prolongs the cell's lifetimes and increases their robustness and ruggedness, thus making them more amenable for field applications. In addition, the small size of spores allows for their easy transport and incorporation in miniaturized portable devices. Finally, we envision that this novel strategy could expand the use of whole-cell biosensors for on-site sensing not only in mild environments but also in harsh environments and locations where there is no easy access to a laboratory, e.g., in developing countries.
引用
收藏
页码:9391 / 9397
页数:7
相关论文
共 32 条
[1]   Arsenic: Health effects, mechanisms of actions, and research issues [J].
Abernathy, CO ;
Liu, YP ;
Longfellow, D ;
Aposhian, HV ;
Beck, B ;
Fowler, B ;
Goyer, R ;
Menzer, R ;
Rossman, T ;
Thompson, C ;
Waalkes, M .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 (07) :593-597
[2]  
[Anonymous], PHOTOPROTEINS BIOANA
[3]   Microbial whole-cell sensing systems of environmental pollutants [J].
Belkin, S .
CURRENT OPINION IN MICROBIOLOGY, 2003, 6 (03) :206-212
[4]   Advances in preservation methods:: keeping biosensor microorganisms alive and active [J].
Bjerketorp, J ;
Håkansson, S ;
Belkin, S ;
Jansson, JK .
CURRENT OPINION IN BIOTECHNOLOGY, 2006, 17 (01) :43-49
[5]  
Black MM, 2003, J NUTR, V133, p1473S, DOI 10.1093/jn/133.5.1473S
[6]   Genetically engineered whale-cell sensing systems: Coupling biological recognition with reporter genes [J].
Daunert, S ;
Barrett, G ;
Feliciano, JS ;
Shetty, RS ;
Shrestha, S ;
Smith-Spencer, W .
CHEMICAL REVIEWS, 2000, 100 (07) :2705-2738
[7]   METALLOREGULATION OF THE CYANOBACTERIAL SMT LOCUS - IDENTIFICATION OF SMTB BINDING-SITES AND DIRECT INTERACTION WITH METALS [J].
ERBE, JL ;
TAYLOR, KB ;
HALL, LM .
NUCLEIC ACIDS RESEARCH, 1995, 23 (13) :2472-2478
[8]  
FELICIANO J, 2006, PHOTOPROTEINS BIOANA, P131
[9]   Whole cell strategies based on lux genes for high throughput applications toward new antimicrobials [J].
Galluzzi, Lorenzo ;
Karp, Matti .
COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2006, 9 (07) :501-514
[10]  
Gu MB, 2004, ADV BIOCHEM ENG BIOT, V87, P269