scholarly journals High pressure inertial focusing for separation and concentration of bacteria at high throughput

2017 ◽  
Vol 922 ◽  
pp. 012001
Author(s):  
F.J. Cruz ◽  
K. Hjort
2017 ◽  
Vol 27 (8) ◽  
pp. 084001 ◽  
Author(s):  
J Cruz ◽  
S Hooshmand Zadeh ◽  
T Graells ◽  
M Andersson ◽  
J Malmström ◽  
...  

2013 ◽  
Vol 28 (S2) ◽  
pp. S360-S370 ◽  
Author(s):  
F. Fauth ◽  
I. Peral ◽  
C. Popescu ◽  
M. Knapp

The current report describes the installation and the preliminary commissioning of the Material Science Powder Diffraction (MSPD) beamline at the Spanish synchrotron ALBA-CELLS. The beamline is fully dedicated to powder diffraction techniques and consists of two experimental stations positioned in series: a High Pressure/Microdiffraction station and a High Resolution/High Throughput powder diffraction station.


2004 ◽  
Vol 48 (3) ◽  
pp. 897-902 ◽  
Author(s):  
Thérèse Stachyra ◽  
Christophe Dini ◽  
Paul Ferrari ◽  
Ahmed Bouhss ◽  
Jean van Heijenoort ◽  
...  

ABSTRACT We have developed a novel assay specific to MraY, which catalyzes the first membrane step in the biosynthesis of bacterial cell wall peptidoglycan. This was accomplished by using UDP-MurNAc-Nε -dansylpentapeptide, a fluorescent derivative of the MraY nucleotide substrate, and a partially purified preparation of MraY solubilized from membranes of an Escherichia coli overproducing strain. Two versions of the assay were developed, one consisting of the high-pressure liquid chromatography separation of the substrate and product (dansylated lipid I) and the other, without separation and adapted to the high-throughput format, taking advantage of the different fluorescence properties of the nucleotide and lipid I in the reaction medium. The latter assay was validated with a set of natural and synthetic MraY inhibitors.


2012 ◽  
Vol 113 (6) ◽  
pp. 788-791 ◽  
Author(s):  
Toshimi Hasegawa ◽  
Manabu Hayashi ◽  
Kazuki Nomura ◽  
Mayumi Hayashi ◽  
Miyuki Kido ◽  
...  

2007 ◽  
Vol 55 (2) ◽  
pp. 209-224 ◽  
Author(s):  
M. Walid Qoronfleh ◽  
Lyndal K. Hesterberg ◽  
Matthew B. Seefeldt

2003 ◽  
Vol 216 (1-2) ◽  
pp. 110-119 ◽  
Author(s):  
C. Kiener ◽  
M. Kurtz ◽  
H. Wilmer ◽  
C. Hoffmann ◽  
H.-W. Schmidt ◽  
...  

2022 ◽  
Vol 32 (2) ◽  
pp. 025007
Author(s):  
Shuang Chen ◽  
Zongqian Shi ◽  
Jiajia Sun ◽  
Shenli Jia ◽  
Mingjie Zhong ◽  
...  

Abstract Inertial microfluidic has been widely applied to manipulate particles or bio-sample based on the inertial lift force and Dean Vortices. This technology provides significant advantages over conventional technologies, including simple structure, high throughput and freedom from an external field. Among many inertial microfluidic systems, the straight microchannel is commonly used to produce inertial focusing, which is a phenomenon that particles or cells are aligned and separated based on their size under the influence of inertial lift force. Besides the inertial lift force, flow drag forces induced by the geometrical structures of microchannel can also affect particle focusing. Herein, a split-recombination microchannel, consisting of curved and straight channels, is proposed to focus and separate particles at high flow rate. As compared with the straight channel, the particle focusing in the split-recombination channel is greatly improved, which results from the combined effects of the inertial lift force, the curvature-induced Dean drag force and the structure of split and recombination. Moreover, the distribution of different-sized particles in designed microchannel is investigated. The results indicate that the proposed microchannel not only enhances the particle focusing but also enables the separation of different-sized particles with high throughput. Finally, it is discovered that the larger length of straight channel and curvature radius of curved channel can result in a more efficient particle separation. Another important feature of designed split-recombination microchannel is that it can be arranged in parallel to handle large-volume samples, holding great potential in lab-on-a-chip applications.


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