Chromatographic separation and mass spectrometric analysis of N-acetyl-l-cysteine-protected palladium nanoparticles

2017 ◽  
Vol 9 (31) ◽  
pp. 4539-4546 ◽  
Author(s):  
Lei Zhang ◽  
Qin Hu ◽  
Zhongping Li ◽  
Yan Zhang ◽  
Dongtao Lu ◽  
...  

The NAC-PdNPs product was successfully separated by reverse-phase HPLC, and the collected NAC-PdNPs fractions were characterised by MALDI-TOF MS.

Vsyo o myase ◽  
2021 ◽  
pp. 56-58
Author(s):  
Yu.K. Yushina ◽  
◽  
D.S. Bataeva ◽  
E.V. Zayko ◽  
N.A. Nasyrov ◽  
...  

2018 ◽  
Vol 08 (03) ◽  
pp. 251-263 ◽  
Author(s):  
Mathias Groll ◽  
Jochen Frenzel ◽  
Matthias Krause ◽  
Anne Schänzer ◽  
Wolf Müller ◽  
...  

2011 ◽  
Vol 123 (8) ◽  
pp. 1841-1844 ◽  
Author(s):  
Antonio Sanchez-Ruiz ◽  
Sonia Serna ◽  
Nerea Ruiz ◽  
Manuel Martin-Lomas ◽  
Niels-Christian Reichardt

Author(s):  
Alexsey Gladchuk ◽  
Julia Schumilina ◽  
Alena Kusnetsova ◽  
Ksenia Bureiko ◽  
Alexander Tsarev ◽  
...  

Fatty acids (FAs) represent an important class of metabolites, impacting on membrane building blocks and cellular regulatory networks. In nature, prokaryotes are characterized with the most impressing FA structural diversity and the highest relative contents of free fatty acids (FFAs). Thereby, nitrogen-fixing bacteria (order Rhizobiales), often found in symbiosis with legumes, attract a special interest. Indeed, FAs impact on the structure of rhizobial nodulation factors, required for successful infection of plant root. Although the FA patterns can be addressed by GC- and LC-MS, these methods are time-consuming and suffer from compromised sensitivity, low stability of derivatives and artifacts. In contrast, MALDI-TOF-MS represents an excellent platform for high-efficient metabolite fingerprinting, also applicable to FFAs. Therefore, here we propose a simple and straightforward protocol for high-throughput relative quantification of FFAs in rhizobia by the combination of Langmuir technology and MALDI-TOF-MS, which is featured with high sensitivity, accuracy and precision of quantification. Here we propose a step by step procedure comprising rhizobia culturing, pre-cleaning, extraction, sample preparation, mass spectrometric analysis, data processing and post-processing. To demonstrate the analytical potential of the protocol we illustrate it by a case study – comparison the FFA metabolomes of two rhizobia species - Rhizobium leguminosarum and Sinorhizobium meliloti.


1998 ◽  
Vol 70 (18) ◽  
pp. 3840-3844 ◽  
Author(s):  
Rudi Grimm ◽  
Helen Birrell ◽  
Gordon Ross ◽  
Joanne Charlwood ◽  
Patrick Camilleri

2011 ◽  
Vol 50 (8) ◽  
pp. 1801-1804 ◽  
Author(s):  
Antonio Sanchez-Ruiz ◽  
Sonia Serna ◽  
Nerea Ruiz ◽  
Manuel Martin-Lomas ◽  
Niels-Christian Reichardt

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