System for on-site environment monitoring
An environment, monitoring environment technology, applied in data processing applications, ICT adaptation, healthcare resources or facilities, etc., can solve problems such as high false positive rate
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example 1
[0182] Example 1: A system for monitoring the environment
[0183] Identify thirteen testing sites on the floor plan of the food production facility. Test points include historical hotspots. The marked floor plan is converted to a png file and imported into software that identifies and tracks test locations within the floor plan. The marked test points are: quick freezing room (drainage system 1), quick freezing room (drainage system 2), quick freezing room (drainage system 3), quick freezing room (drainage system 4), cold storage (drainage system 5), quick freezing room (drainage system System 6), quick-freezing room (drainage system 7), quick-freezing room (balance), cold storage (guide flushing drainage system), quick-freezing room (oil drip tray 1), quick-freezing room (water receiver 2), quick-freezing room (forklift) and quick freezer (drainage close to the door). The test sites were divided into three groups for weekly testing.
[0184] Historical test data for this...
example 2
[0451] Example 2: Detection of bacteria with engineered phages
[0452] In this example, a relatively low number of E. coli NEB-10β cells was associated with 3xl0 8 PFU / mL of the engineered antibiotic T3::0.7 luc was mixed and luciferase production was measured every ten minutes by removing 20 μL of the lysate and combining it with 100 μL of the luciferin-containing detection reagent. ( Figure 11 . ) to prepare three different concentrations of cells in triplicate. Using 10-fold serial dilutions (from 10 0 to 10 -8 10-fold dilution of ) the number of bacteria present in each sample was determined after the experiment. Using this method, test samples were determined to have concentrations of E. coli of 6 (±4.6), 60 (±45.8) and 600± (458.0) cells. For the two higher concentrations (60 and 600), maximum light production in the sample was observed 40 min after the addition of the phage. However, a detectable signal was measured above the lower limit of detection at 20 minu...
example 3
[0455] Example 3: Detection of bacteria with engineered phages
[0456] The experiment was designed and performed to determine the minimum time of detection in the T3::0.7 luc / E. coli pairing.
[0457] Logarithmic phase culture of E. coli (2.5xl0 7 CFU / mL) by 3xl0 8 Infect with PFU / mL of T3::0.7 luc and aliquot 20 μL in microtubes. Every ten minutes, triple reads were obtained by measuring light production from triplicate aliquots by adding 100 μL of Promega luciferase assay reagent. exist Figure 12 The results are shown in .
[0458] We found that the first time we measured cultures at 10 min post-infection, there was already a substantial signal for detection (51,393 ± 28,152 RLU). As in previous experiments, the time to maximize the generated signal was 40 minutes.
[0459] Extrapolated backward from the 10 minute time point, these data imply detection at 5 minutes.
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