Microbial inactivation of Pseudomonas putida and Pichia pastoris using gene silencing.


Autoria(s): Morse, TO; Morey, SJ; Gunsch, CK
Data(s)

01/05/2010

Formato

3293 - 3297

Identificador

http://www.ncbi.nlm.nih.gov/pubmed/20364871

Environ Sci Technol, 2010, 44 (9), pp. 3293 - 3297

0013-936X

http://hdl.handle.net/10161/4030

Idioma(s)

ENG

en_US

Relação

Environ Sci Technol

10.1021/es901404a

Environmental science & technology

Tipo

Journal Article

Cobertura

United States

Resumo

Antisense deoxyoligonucleotide (ASO) gene silencing was investigated as a potential disinfection tool for industrial and drinking water treatment application. ASOs bind with their reverse complementary mRNA transcripts thereby blocking protein translation. While ASO silencing has mainly been studied in medicine, it may be useful for modulating gene expression and inactivating microorganisms in environmental applications. In this proof of concept work, gene targets were sh ble (zeocin resistance) and todE (catechol-2,3-dioxygenase) in Pichia pastoris and npt (kanamycin resistance) in Pseudomonas putida. A maximum 0.5-fold decrease in P. pastoris cell numbers was obtained following a 120 min incubation with single-stranded DNA (ssDNA) concentrations ranging from 0.2 to 200 nM as compared to the no ssDNA control. In P. putida, a maximum 5.2-fold decrease was obtained after 90 min with 400 nM ssDNA. While the silencing efficiencies varied for the 25 targets tested, these results suggest that protein activity as well as microbial growth can be altered using ASO gene silencing-based tools. If successful, this technology has the potential to eliminate some of the environmental and health issues associated with the use of strong chemical biocides. However, prior to its dissemination, more research is needed to increase silencing efficiency and develop effective delivery methods.

Palavras-Chave #Colony Count, Microbial #DNA, Single-Stranded #Disinfection #Drug Resistance, Bacterial #Environmental Microbiology #Gene Silencing #Genetic Techniques #Kanamycin Resistance #Microbial Sensitivity Tests #Oligonucleotides, Antisense #Pichia #Pseudomonas putida #RNA, Messenger #Time Factors