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Uv vis du 640

Manufactured by Beckman Coulter
Sourced in United States

The UV-VIS DU 640 is a spectrophotometer designed for ultraviolet and visible light absorption measurements. It is capable of performing accurate and reliable absorbance and transmittance measurements across a wide range of wavelengths. The instrument provides a user-friendly interface and advanced features to support various analytical applications in research and clinical laboratories.

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5 protocols using uv vis du 640

1

Growth Evaluation of Stressed Yeasts

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US-treated yeasts were inoculated in YPG broth to 3 log CFU/mL; the medium was supplemented with NaCl (2–5%-stress conditions for the strains used in this research) and incubated at 25 °C (yeast optimal temperature) or 37 °C (temperature of human body; probiotic properties for yeasts). Growth was evaluated after 24 and 48 h at an absorbance of 600 nm using a spectrophotometer UV–Vis DU 640 Beckman (Fullerton, CA, USA).
The results were modelled as the growth index [28 (link)] modified by Racioppo et al. [19 (link)]:
where Abss is the absorbance of US-treated strain and Absc is the absorbance of the control (untreated microorganism, combination A1).
GI was analyzed as suggested by Bevilacqua et al. [28 (link)] and modified as follows:

GI < 25%: complete inhibition;

25% < GI < 75%: partial inhibition;

GI > 75%: no inhibition.

A new class was added to point out a positive effect on yeast growth:

GI > 120%: growth enhancement.

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2

Alicyclobacilli Growth Assessment Protocol

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Growth profile of alicyclobacilli was assessed as follows:
The samples were inoculated to 6 log cfu/ml with either cells or spores and incubated for 7 days: growth was assessed every day by measuring absorbance at 420 nm through a spectrophotometer UV-VIS DU 640 Beckman (Fullerton, CA).
Results from phenotyping were converted into quali-quantitative codes (0, no growth or no enzymatic activity; 1, growth or positive enzymatic activity) and used as input data to run a cluster analysis through the add-in component of Excel XLSTAT (Addinsoft, Paris, France).
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3

Growth Assay of US-Treated Bacterial Strains

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US-treated strains were inoculated in MRS broth to 5 log CFU/mL; the medium was supplemented with 3 or 6% NaCl or incubated at 45 °C. Growth was evaluated after 24 and 48 h as absorbance at 600 nm using a spectrophotometer UV–Vis DU 640 Beckman (Fullerton, CA, USA).
The results were modelled as Growth Index modified by Racioppo et al. [17] (link): GI=Abss/Absc*100 where: Abss is the absorbance of US-treated strain and Absc is the absorbance of control (untreated microorganism, combination A1).

GI was analysed as follows:

GI < 25%: complete inhibition;

25% < GI < 75%: partial inhibition;

GI > 75%: no inhibition.

GI > 120%: growth enhancement.

Viable count was also evaluated after 24 and 48 h.

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4

Protein Quantification in Bacterial Samples

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Untreated and treated samples (5–6 log cfu/ml) were centrifuged at 6,000 x g for 10 min. Then, 2.0 ml of BSA working reagent (BSA Protein Assay Reagent Kit, Sigma-Aldrich) was added to 0.1 ml of supernatant and incubated at 60°C for 15 min. After that, the absorbance at 562 nm was determined [spectrophotometer UV-VIS DU 640 Beckman (Fullerton, CA)]. The calibration curve was built by using BSA as a standard (29 (link)).
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5

Spore Suspension UV Absorbance Analysis

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Spores suspensions were centrifuged at 1200× g for 10 min and the UV absorbance of the supernatant was measured at 260 nm and at 280 nm with a spectrophotometer (spectrophotometer UV-VIS DU 640 Beckman (Fullerton, CA, USA) [17 (link)].
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