scholarly journals Monitoring Genetic and Metabolic Potential for In-Situ Bioremediation: Mass Spectrometry

2000 ◽  
Author(s):  
Michelle V Buchanan ◽  
Phillip F Britt ◽  
Mitchel J Doktycz ◽  
Gregory B Hurst ◽  
Mary E Lidstrom

10.2172/13439 ◽  
1998 ◽  
Author(s):  
M.V. Buchanan ◽  
G.B. Hurst ◽  
M.J. Doktycz ◽  
P.F. Britt ◽  
K. Weaver ◽  
...  


10.2172/13438 ◽  
1997 ◽  
Author(s):  
M.V. Buchanan ◽  
G.B. Hurst ◽  
P.F. Britt ◽  
S.A. McLuckey ◽  
M.J. Doktycz


1999 ◽  
Author(s):  
Michelle V Buchanan ◽  
Gregory B Hurst ◽  
Mary E Lidstrom ◽  
Anne Auman ◽  
Phillip F Britt ◽  
...  


Microbiology ◽  
2004 ◽  
Vol 150 (6) ◽  
pp. 1785-1796 ◽  
Author(s):  
Martin Welker ◽  
Matthias Brunke ◽  
Karina Preussel ◽  
Indra Lippert ◽  
Hans von Döhren

Microcystis sp. has been recognized in recent years as a producer of a high number of secondary metabolites. Among these, peptides that are produced by the non-ribosomal peptide synthetase pathway often show bioactivity or are toxic to humans. The production of particular peptides is specific for individual Microcystis clones, allowing their characterization as chemotypes by analysing the peptidome. The authors studied the in situ diversity of peptides and chemotypes in Microcystis communities from lakes in and around Berlin, Germany, by direct analysis of individual colonies by MALDI-TOF mass spectrometry. From 165 colonies analysed a total of 46 individual peptides could be identified, 21 of which have not been described previously. For six of the new peptides the structures could be elucidated from fragment patterns, while for others only a preliminary classification could be achieved. In most colonies, two to ten individual peptides were detected. In 19 colonies, 16 of which were identified as M. wesenbergii, no peptide metabolites could be detected. The peptide data of 146 colonies were subjected to an ordination (principal components analysis). The principal components were clearly formed by the microcystin variants Mcyst-LR, -RR and -YR, anabaenopeptins B and E/F, a putative microviridin, and a new cyanopeptolin. In the resulting ordination plots most colonies were grouped into five distinct groups, while 40 colonies scattered widely outside these groups. In some cases colonies from different lakes clustered closely, indicating the presence of similar chemotypes in the respective samples. With respect to colony morphology no clear correlation between a chemotype and a morphospecies could be established, but M. aeruginosa, for example, was found to produce predominantly microcystins. In contrast, M. ichthyoblabe colonies were mostly negative for microcystins and instead produced anabaenopeptins. The number of peptides detected in a limited number of samples and the various combinations of peptides in individual Microcystis colonies highlights the immense metabolic potential and diversity of this genus.



2006 ◽  
Vol 14 (2) ◽  
pp. 478-482
Author(s):  
Jamie Robinson ◽  
Russell Thomas ◽  
Steve Wallace ◽  
Paddy Daly ◽  
Robert Kalin


2020 ◽  
Author(s):  
Feifei Jia ◽  
Jie Wang ◽  
Yanyan Zhang ◽  
Qun Luo ◽  
Luyu Qi ◽  
...  

<p></p><p><i>In situ</i> visualization of proteins of interest at single cell level is attractive in cell biology, molecular biology and biomedicine, which usually involves photon, electron or X-ray based imaging methods. Herein, we report an optics-free strategy that images a specific protein in single cells by time of flight-secondary ion mass spectrometry (ToF-SIMS) following genetic incorporation of fluorine-containing unnatural amino acids as a chemical tag into the protein via genetic code expansion technique. The method was developed and validated by imaging GFP in E. coli and human HeLa cancer cells, and then utilized to visualize the distribution of chemotaxis protein CheA in E. coli cells and the interaction between high mobility group box 1 protein and cisplatin damaged DNA in HeLa cells. The present work highlights the power of ToF-SIMS imaging combined with genetically encoded chemical tags for <i>in situ </i>visualization of proteins of interest as well as the interactions between proteins and drugs or drug damaged DNA in single cells.</p><p></p>



2009 ◽  
Author(s):  
Paul Hatzinger ◽  
Jay Diebold


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