Comment on “Modelling the PAO–GAO competition: Effects of carbon source, pH and temperature” by Lopez-Vazquez, C.M., Oehmen, A., Hooijmans, C.M., Brdjanovic, D., Gijzen, H.J., Yuan, Z., van Loosdrecht, M.C.M. Water Res. (2009)

2009 ◽  
Vol 43 (11) ◽  
pp. 2947-2949 ◽  
Author(s):  
Dwight Houweling ◽  
Yves Comeau ◽  
Imre Takács ◽  
Peter Dold
2009 ◽  
Vol 43 (11) ◽  
pp. 2950-2951 ◽  
Author(s):  
Mark C.M. van Loosdrecht ◽  
Adrian Oehmen ◽  
Christine M. Hooijmans ◽  
Damir Brdjanovic ◽  
Huub J. Gijzen ◽  
...  

2009 ◽  
Vol 43 (2) ◽  
pp. 450-462 ◽  
Author(s):  
Carlos M. Lopez-Vazquez ◽  
Adrian Oehmen ◽  
Christine M. Hooijmans ◽  
Damir Brdjanovic ◽  
Huub J. Gijzen ◽  
...  

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


2018 ◽  
Author(s):  
Zhanyu Li ◽  
Mengru Zhang ◽  
Yu Zhang ◽  
Shuang Liu ◽  
Jinbo Zhao ◽  
...  

Deployment of organoboron in lieu of the strongly basic <br>organometallic reagents as carbon source in Cu-catalyzed <br>cyclopropene carbometallation opens unprecedented three-<br>component reactivity for stereoselective synthesis of poly-substituted cyclopropanes. A proof-of-principle demonstration of this novel carbometallation strategy is presented herein for a highly convergent access to poly-substituted aminocyclopropane framework via <br>carboamination. Preliminary results on asymmetric desymmetrization with commercial bisphosphine ligands attained high levels of enantioselection, offering a straightforward access to enantioenriched aminocyclopropanes bearing all-three chiral centers, including an all-carbon quaternary center. This strategy may underpin a host of novel synthetic protocols for poly-substituted cyclopropanes. <br>


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