scholarly journals Microbiological Assay Method for Sulfate in Rain Water by Means of Cultivation of Escherichia coli

Eisei kagaku ◽  
1969 ◽  
Vol 15 (6) ◽  
pp. 331-334 ◽  
Author(s):  
TAKEO YAMAMOTO ◽  
HIROSHI OBA
1976 ◽  
Vol 22 (1) ◽  
pp. 76-82 ◽  
Author(s):  
R. A. Scudamore ◽  
M. Goldner

A microbiological assay method has been developed and applied to Neisseria gonorrhoeae, for the purpose of detecting enzymatic deactivation of benzyl penicillin. Calibration of the method, using strains of Escherichia coli K-12 with previously reported penicillinase (EC 3.5.2.6.) activities, has shown that it is extremely sensitive and may be used in a quantitative manner. At the limit of sensitivity the test is able to detect penicillin breakdown in the order of 3 × 10−3 μg in 48 h, which is equivalent to about 7 × 10−8 μmol/min per milligram dry weight of cells. Over 100 strains of N. gonorrhoeae, most of them resistant to penicillin, were screened for their ability to deactivate penicillin during 48 h of growth in the presence of subinhibitory levels. No deactivation was detected. It is concluded, from quantitative evidence, that reduced penicillin sensitivity in N. gonorrhoeae is not due to the enzymatic deactivation of the antibiotic.


1943 ◽  
Vol 148 (2) ◽  
pp. 281-287
Author(s):  
Roy C. Thompson ◽  
Edith R. Isbell ◽  
Herschel K. Mitchell

1977 ◽  
Vol 60 (1) ◽  
pp. 179-182
Author(s):  
H Latham Breunig ◽  
Robert E Scroggs ◽  
Lealon V Tonkinson ◽  
Henry Bikin

Abstract A turbidimetric microbiological assay method for monensin in chicken rations was submitted in a modified form to 8 collaborating laboratories along with randomized and coded samples. Three laboratories used the manual method and 5 used the automated method. Other factors in the experimental design were ration types (broiler starter, broiler finisher, and pullet grower), feed form (meal vs. pellets), and potency level (90 and 110 g/ton) for one ration. Average recoveries for the ration types over all laboratories and feed forms were 87.7—93.13% of label, while mean recoveries in 2 feed forms were 91.7% for meal and 87.6% for pellets. Average recoveries in the 8 laboratories ranged from 84.6 to 106.64% of label for 90 g/ton rations and 87.1 to 106.6% for 110 g/ton rations. There was no significant difference between the manual and the automated methods. The collaborators’ assays were uniform with respect to within-laboratory variation. Relative standard deviations ranged from 4.51 to 10.76% with a median of 6.04%. Agreement with the plate assay is quite good. The turbidimetric method for monensin has been adopted as official first action.


2020 ◽  
Vol 4 ◽  
Author(s):  
Hsin-Bai Yin ◽  
Nidhi Gupta ◽  
Chi-Hung Chen ◽  
Ashley Boomer ◽  
Abani Pradhan ◽  
...  

Treated wastewater (TW) and roof-collected rain water (RW) that meet the required microbial quality as per Food Safety Modernization Act (FSMA) regulation may serve as alternative irrigation water sources to decrease the pressure on the current water scarcity. Alternative water sources may have different water characteristics that influence the survival and transfer of microorganisms to the irrigated produce. Further, these water sources may contain pathogenic bacteria such as Shiga-toxigenic Escherichia coli. To evaluate the risk associated with TW and RW irrigation on the fresh produce safety, the effect of TW and RW irrigation on the transfer of two non-pathogenic E. coli strains as surrogates for E. coli O157:H7 to different lettuce cultivars grown in the field was investigated. Lettuce cultivars “Annapolis,” “Celinet,” and “Coastline” were grown in the field at the Fulton farm (Chambersburg, PA). Approximately 10 days before harvest, lettuce plants were spray-irrigated with groundwater (GW), TW, or RW containing 6 log CFU ml−1 of a mixture of nalidixic acid-resistant E. coli O157:H12 and chloramphenicol-resistant E. coli K12 in fecal slurry as non-pathogenic surrogates for E. coli O157:H7. On 0, 1, 3, 7, and 10 days post-irrigation, four replicate lettuce leaf samples (30 g per sample) from each group were collected and pummeled in 120 ml of buffered peptone water for 2 min, followed by spiral plating on MacConkey agars with antibiotics. Results showed that the recovery of E. coli O157:H12 was significantly greater than the populations of E. coli K12 recovered from the irrigated lettuce regardless of the water sources and the lettuce cultivars. The TW irrigation resulted in the lowest recovery of the E. coli surrogates on the lettuce compared to the populations of these bacteria recovered from the lettuce with RW and GW irrigation on day 0. The difference in leaf characteristics of lettuce cultivars significantly influenced the recovery of these surrogates on lettuce leaves. Populations of E. coli O157:H12 recovered from the RW-irrigated “Annapolis” lettuce were significantly lower than the recovery of this bacterium from the “Celinet” and “Coastline” lettuce (P < 0.05). Overall, the recovery of specific E. coli surrogates from the RW and TW irrigated lettuce was comparable to the lettuce with the GW irrigation, where GW served as a baseline water source. E. coli O157:H12 could be a more suitable surrogate compared to E. coli K12 because it is an environmental watershed isolate. The findings of this study provide critical information in risk assessment evaluation of RW and TW irrigation on lettuce in Mid-Atlantic area.


1970 ◽  
Vol 53 (1) ◽  
pp. 49-53 ◽  
Author(s):  
R M Kline ◽  
R E Stricker ◽  
J D Coffman ◽  
H Bikin ◽  
R P Rathmacher

Abstract A microbiological assay method is described for the coccidiostat monensin in poultry feeds and prerhixes. Samples are extracted with methanol-water (9 + 1), and interfering substances are removed on an alumina column. Microbiological activity in the effluent is measured with Bacillus subtilis (ATCC 6633). Statistical analysis of data from several different rations prepared as meals and pellets indicate a mean recovery and standard deviation of 94.8 ± 9.7 g monensin/ton from a theoretical potency of 110 g monensin/ton. A mean recovery of 98 ± 7.6 µg/g was obtained from samples prepared by fortifying basal rations with t monensin at 110 µg/g Just before extraction.


1989 ◽  
Vol 263 (3) ◽  
pp. 695-702 ◽  
Author(s):  
A M Field ◽  
E Rowatt ◽  
R J P Williams

Lipopolysaccharide from Escherichia coli C interacts with polyvalent cations at low ionic strength at more than one site. The first site has high affinity with a KD value of 10(-8) M for Ca2+ and even stronger binding for [(NH3)5CoNH2Co(NH3)5]5+ and La3+. The high-affinity site for the latter cations is beyond the sensitivity of the assay method. The second, low-affinity, site for bivalent cations has a Km of 10(-3) M, whereas, for tervalent and quinquevalent metal cations and spermine and hexacyclen (1,4,7,10,13,16-hexa-azacyclo-octadecane), this constant has a value of 10(-5) M. Binding of cations to the high-affinity site does not alter the aggregation state of the lipopolysaccharide, but combination with the low-affinity site gives particles twice the size of those of the sodium salt. Very high Ca2+ concentrations (30 mM) give particles eight times the size of those of the sodium salt.


1951 ◽  
Vol 76 (2) ◽  
pp. 341-343 ◽  
Author(s):  
G. G. Villela ◽  
A. Cury

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