A perifusion loop-gap resonator NMR probe for aerobic cell suspensions

1993 ◽  
Vol 29 (4) ◽  
pp. 563-566 ◽  
Author(s):  
Mark E. Anderson ◽  
John L. Markley ◽  
Carles Arùs ◽  
Michael C. Chobanian
1984 ◽  
Vol 30 (11) ◽  
pp. 1397-1404 ◽  
Author(s):  
Russell K. Hynes ◽  
Roger Knowles

Aerobic cell suspensions of Nitrosomonas europaea oxidized ammonium [Formula: see text] to nitrous oxide (N2O) and nitrite [Formula: see text], and exogenous [Formula: see text] in the presence or absence of [Formula: see text] did not stimulate N2O formation. Acetylene (C2H2) inhibited the production of [Formula: see text] and N2O from [Formula: see text] but not from hydroxylamine (NH2OH). The total amount of N2O formed in air was proportional to the amount of [Formula: see text] oxidized; however, the total N2O N formed as a percentage of [Formula: see text] N formed varied very little (0.05–0.15%) over the range of [Formula: see text] concentrations examined (0.05–20.4 mM). Rates of production of N2O and [Formula: see text] showed similar response to pH over the range of 5.4–9.5, with maxima at pH 8.5. Anaerobically, five times more N2O was formed than under aerobic conditions. The highest rates of anaerobic N2O formation were observed in the presence of [Formula: see text] and [Formula: see text] combined (2 and 1 mM, respectively) and C2H2 reduced this rate of N2O formation to that observed with 1 mM[Formula: see text] alone in the presence or absence of C2H2. The presence of the [Formula: see text] oxidizer Nitrobacter winogradskyi had no effect on the formation of N2O by Ns. europaea either in liquid culture or in sterile soil. However, the presence of sterile soil as a suspending matrix increased by 10-fold the production of N2O, and broadened the range of O2 concentrations under which relatively high rates of N2O production occurred. Maximum N2O production by Ns. europaea occurred at 0.75 kPa O2 in liquid suspension and at 2.5 kPa O2 in sterile soil.


Author(s):  
K. Chien ◽  
I.P. Shintaku ◽  
A.F. Sassoon ◽  
R.L. Van de Velde ◽  
R. Heusser

Identification of cellular phenotype by cell surface antigens in conjunction with ultrastructural analysis of cellular morphology can be a useful tool in the study of biologic processes as well as in diagnostic histopathology. In this abstract, we describe a simple pre-embedding, protein A-gold staining method which is designed for cell suspensions combining the handling convenience of slide-mounted cell monolayers and the ability to evaluate specimen staining specificity prior to EM embedding.


1974 ◽  
Vol 77 (1_Suppl) ◽  
pp. S97 ◽  
Author(s):  
K. H. Usadel ◽  
U. Schwedes ◽  
U. Leuschner ◽  
K. Schöffling

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