scholarly journals A Rapid Screening Technique for Bacillus thuringiensis Using Image Processing.

2001 ◽  
Vol 45 (1) ◽  
pp. 9-14 ◽  
Author(s):  
Toshio Hyakutake ◽  
Tokio Ichimatsu ◽  
Eiichi Mizuki ◽  
Michio Ohba
1979 ◽  
Vol 25 (9) ◽  
pp. 1673-1674
Author(s):  
F J Krolikowski ◽  
F T Bell ◽  
B Gerson

2017 ◽  
Vol 80 (4) ◽  
pp. 640-644 ◽  
Author(s):  
Simona Sciuto ◽  
Giovanna Esposito ◽  
Luana Dell'Atti ◽  
Chiara Guglielmetti ◽  
Pier Luigi Acutis ◽  
...  

ABSTRACT Sudan dyes are synthetic azo dyes used by industry in a variety of applications. Classified as carcinogenic, they are not allowed in foodstuffs; however, their presence as adulterants in food products has been regularly reported. Here, we describe an innovative screening method to detect Sudan I, II, III, and IV in tomato sauce, palm oil, and chilli powder. The method entails minimal sample preparation, completely avoiding the liquid chromatography phase, followed by detection and identification through atmospheric pressure chemical ionization time-of-flight mass spectrometry, in positive ionization mode. Analytes were efficiently identified and detected in samples, fortified both with individual analytes and with their mixture, with an error in mass identification less than 5 ppm. Limits of identification of the analytes in the fortified samples were 0.5 to 1 mg/kg, depending on the dye and matrix. The method had a linear range of 0.05 to 5 mg/kg and good linear relationships (R2 > 0.98). Repeatability was satisfactory, with a coefficient of variation lower than 20%. The method was applied to detect the dyes in real adulterated chilli samples, previously found positive by confirmatory high-performance liquid chromatography–mass spectrometry and ELISA, and in commercial products purchased from supermarkets. In all positive samples, analytes were correctly identified with an error in mass identification lower than 5 ppm, while none of the 45 commercial samples analyzed were found to be contaminated. The proposed new assay is sensitive, with a limit of identification, for all the three matrices, complying with the limits defined by the European Union (0.5 to 1 mg/kg) for analytical methods. Compared with conventional methods, the new assay is rapid and inexpensive and characterized by a high throughput; thus, it could be suitable as screening technique to identify Sudan dyes in adulterated food products.


2016 ◽  
Vol 31 (1) ◽  
Author(s):  
Selvaraj Sakthivel ◽  
Prithiviraj Balasubramanian ◽  
Masafumi Nakamura ◽  
Shunkei Ko ◽  
Paromita Chakraborty

AbstractXenobiotic detection systems-chemically activated luciferase expression (XDS-CALUX) bioassay in determining the toxic equivalency (TEQ) of PCDD/Fs from contaminated sites reported in several papers has been discussed in this study. CALUX bioassay method has been validated by an effective combined column clean-up system followed by addition of samples to monolayer cell cultures of H1L6.1c3 cell line in 96 well plates. Cultures are then examined under microscope after 24 h incubation followed by rinsing with 75 μL phosphate buffer saline and 30 μL of cell culture lysis. The response is observed in the luminometer and expressed in relative light unit (RLUs). CALUX-TEQ is estimated from a TCDD standard curve for unknown samples. Quality control in CALUX is done by selecting the range of CALUX values falling in the center of the linear standard curve. For developing nations CALUX biossay can be used as a cost effective and rapid screening technique for screening xenobiotic compounds from the hotspots like open solid waste burning sites, informal e-waste recycling workshops and industrial zones where constant monitoring for such compounds is required.


Weed Science ◽  
1991 ◽  
Vol 39 (4) ◽  
pp. 548-552 ◽  
Author(s):  
Joanna Hubbard ◽  
Ted Whitwell

Measurements of net photosynthesis, chlorophyllafluorescence and solute leakage were evaluated as techniques for rapid detection of grass tolerance to fenoxaprop-ethyl and sethoxydim. Net photosynthesis measured as net CO2uptake of the youngest fully expanded leaf ofCalamagrostis arundinacea‘Karl Foerster’ (Feather Reed Grass) detected tolerance to fenoxaprop-ethyl and susceptibility to sethoxydim 4 days after treatment and prior to the observation of visual injury. Sethoxydim reduced photosynthesis compared to untreated controls but fenoxaprop-ethyl did not. Measurements of older leaf (second most recently fully expanded leaf) photosynthesis were less consistent than those of the younger leaf. Chlorophyllafluorescence ofCalamagrostisleaf segments following treatment with fenoxaprop-ethyl and sethoxydim was ineffective for detecting grass tolerance. Solute leakage from leaf discs treated with 50 to 500 μg ml−1fenoxaprop–ethyl and 10 to 100 μg ml−1sethoxydim indicated differential tolerance ofCalamagrostisand johnsongrass to fenoxaprop–ethyl and centipedegrass and johnsongrass to sethoxydim. Fenoxaprop–ethyl increased solute leakage from susceptible johnsongrass at 100 μg ml−1while the 500 μg ml−1concentration was required to cause substantial solute leakage from tolerantCalamagrostis. Sethoxydim caused greater leakage from johnsongrass than from centipedegrass at 50 and 100 μg ml−1. The best potential rapid screening technique was solute leakage measurements.


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