One-step SFE-plus-C 18 selective extraction of low-polarity compounds, with lipid removal, from smoked fish and bovine milk

2002 ◽  
Vol 374 (5) ◽  
pp. 923-931 ◽  
Author(s):  
Md. Ali ◽  
Richard Cole
1985 ◽  
Vol 48 (12) ◽  
pp. 1019-1021 ◽  
Author(s):  
BRUCE R. BEATTY ◽  
RALPH J. FARNSWORTH ◽  
ARNOLD J. LUND ◽  
RICHARD H. LYON ◽  
GILBERT E. WARD

A medium which incorporates CAMP factor produced by Streptococcus agalactiae (group B) into sheep blood agar was used to culture and identify coagulase-positive staphylococci from bovine milk. Of 506 staphylococcal isolates from bovine milk, 92.5% of coagulase-positive organisms produced a wide zone of complete hemolysis, whereas 98.9% of coagulase-negative organisms did not. The agreement of this one-step culture and identification test with the standard tube coagulase test was higher than that of the deoxyribonuclease test medium, Baird-Parker egg yolk medium, tellurite glycine medium and slide coagulase tests.


Author(s):  
Jean-Paul Perraudin ◽  
◽  
Léo De Valck ◽  

Today, the industrial scale production of lactoferrin is carried out in one step by extraction from bovine milk or whey. As the role of lactoferrin in the milk is to protect the liquid against the bacterial contamination binding the lipopolysaccharides (LPS) of those bacteria, it is not surprising that the lactoferrin extracted from milk is covered by bacterial LPS, losing the most part of its biological activities. It is absolutely crucial that the production of Lactoferrin consists to a two steps process. The first step consists to extract from milk or from whey a solution that we called lactenin which contains different molecules including lactoferrin, lactoperoxidase, angiogenin and some other minor components. The second step consists to purify the lactoferrin from the other components including the LPS. Only under such conditions, we could recuperate a high level pure molecule with all its biological activities as it is not done actually


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Indra Gandi Subramani ◽  
Veeradasan Perumal ◽  
Subash C. B. Gopinath ◽  
Norani Muti Mohamed ◽  
Mark Ovinis ◽  
...  

AbstractThe bovine milk allergenic protein, ‘β-lactoglobulin’ is one of the leading causes of milk allergic reaction. In this research, a novel label-free non-faradaic capacitive aptasensor was designed to detect β-lactoglobulin using a Laser Scribed Graphene (LSG) electrode. The graphene was directly engraved into a microgapped (~ 95 µm) capacitor-electrode pattern on a flexible polyimide (PI) film via a simple one-step CO2 laser irradiation. The novel hybrid nanoflower (NF) was synthesized using 1,1′-carbonyldiimidazole (CDI) as the organic molecule and copper (Cu) as the inorganic molecule via one-pot biomineralization by tuning the reaction time and concentration. NF was fixed on the pre-modified PI film at the triangular junction of the LSG microgap specifically for bio-capturing β-lactoglobulin. The fine-tuned CDI-Cu NF revealed the flower-like structures was viewed through field emission scanning electron microscopy. Fourier-transform infrared spectroscopy showed the interactions with PI film, CDI-Cu NF, oligoaptamer and β-lactoglobulin. The non-faradaic sensing of milk allergen β-lactoglobulin corresponds to a higher loading of oligoaptamer on 3D-structured CDI-Cu NF, with a linear range detection from 1 ag/ml to 100 fg/ml and attomolar (1 ag/ml) detection limit (S/N = 3:1). This novel CDI-Cu NF/LSG microgap aptasensor has a great potential for the detection of milk allergen with high-specificity and sensitivity.


2021 ◽  
Vol 31 (6) ◽  
pp. 1828-1841
Author(s):  
Qing-hua TIAN ◽  
Xiang-dong GAN ◽  
Da-wei YU ◽  
Fu-hui CUI ◽  
Xue-yi GUO

2013 ◽  
Vol 136 (2) ◽  
pp. 864-870 ◽  
Author(s):  
Ali Atasever ◽  
Hasan Ozdemir ◽  
Ilhami Gulcin ◽  
O. Irfan Kufrevioglu

1996 ◽  
Vol 63 (1) ◽  
pp. 73-81 ◽  
Author(s):  
Christine Prin ◽  
Nezha El Bari ◽  
Paul Montagne ◽  
Marie-Louise Cuilliere ◽  
Marie-Christine Bene ◽  
...  

SummaryA microparticle-enhanced nephelometric immunoassay has been developed for the determination of caseinomacropeptide (CMP) in bovine milk. It is based on the nephelometric quantification of the competitive immunoagglutination of a microparticle–CMP conjugate with an anti-κ-casein (κ-CN) antiserum. This one step immunoassay was sensitive (detection limit in reaction mixture, 16μg/l), accurate (linear recovery of CMP in dilution overloading) and reproducible (CV 7–14% for within and between run precision). Because of the specificity of the polyclonal antiserum used, it was necessary to separate CMP from κ-CN by ultrafiltration before the quantification of bovine milk CMP. Under the conditions of milk ultrafiltration used, κ-CN was entirely retained (> 99·5%) but the concentration of CMP measured in milk ultrafiltrates was underestimated (by ∼25%) compared with its concentration in whole milk. Microparticle-enhanced nephelometric immunoassay of CMP, with a calibration range from 0·32 to 20 mg/1 for 20- fold diluted milk ultrafiltrate, allowed contamination of bovine milk by rennet whey as low as 5 ml/1 to be detected. Applied to ultrafiltrates from milk stored at 4 °C, this immunoassay also detected proteolysis of κ-CN not revealed by measurement of κ-CN concentration in milk. A statistical lower limit of 3·21 mg/1 was determined as the increase in CMP concentration in milk ultrafiltrates that indicated probable κ-CN proteolysis in the milk sample. Previously demonstrated to be an easy to perform method for assaying the main proteins of bovine milk, microparticle-enhanced nephelometric immunoassay thus also appeared to be appropriate to quantify CMP so as to detect slight contamination of milk by whey and to indicate the proteolysis of κ-CN during milk storage at low temperature.


2017 ◽  
Vol 38 (19) ◽  
pp. 2456-2461 ◽  
Author(s):  
Camille Perréard ◽  
Fanny d'Orlyé ◽  
Sophie Griveau ◽  
Baohong Liu ◽  
Fethi Bedioui ◽  
...  

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