Simultaneous removals of nitrate and sulfate and the adverse effects of gravel-based biofilters with flower straws added as exogenous carbon source

2016 ◽  
Vol 95 ◽  
pp. 189-197 ◽  
Author(s):  
Jun-jun Chang ◽  
Yi-Feng Lu ◽  
Jin-quan Chen ◽  
Xiao-yun Wang ◽  
Tong Luo ◽  
...  
2017 ◽  
Vol 42 (4) ◽  
pp. 1970-1976 ◽  
Author(s):  
Dennapa Sengmee ◽  
Benjamas Cheirsilp ◽  
Thanwadee Tachapattaweawrakul Suksaroge ◽  
Poonsuk Prasertsan

2014 ◽  
Vol 37 (8) ◽  
pp. 1497-1505 ◽  
Author(s):  
Érika Cristina Francisco ◽  
Telma Teixeira Franco ◽  
Roger Wagner ◽  
Eduardo Jacob-Lopes

1971 ◽  
Vol 17 (9) ◽  
pp. 1179-1184 ◽  
Author(s):  
Françoise Vezinhet ◽  
A. Arnaud ◽  
P. Galzy

During the process of sporulation, the oxidation rate of exogenous carbon source, acetic acid, is high during a period lasting from 1 to 4 h. Then it falls rapidly and the metabolism of acetic acid seems to be deflected. Endogenous oxidation rate rises rapidly at the beginning of the process and reaches its maximum after a 12- to 16-h contact with the sporulation medium. Then it falls regularly.


2000 ◽  
Vol 182 (20) ◽  
pp. 5916-5918 ◽  
Author(s):  
René Handrick ◽  
Simone Reinhardt ◽  
Dieter Jendrossek

ABSTRACT Ralstonia eutropha H16 degraded (mobilized) previously accumulated poly(3-hydroxybutyrate) (PHB) in the absence of an exogenous carbon source and used the degradation products for growth and survival. Isolated native PHB granules of mobilized R. eutropha cells released 3-hydroxybutyrate (3HB) at a threefold higher rate than did control granules of nonmobilized bacteria. No 3HB was released by native PHB granules of recombinant Escherichia coli expressing the PHB biosynthetic genes. Native PHB granules isolated from chromosomal knockout mutants of an intracellular PHB (i-PHB) depolymerase gene of R. eutropha H16 and HF210 showed a reduced but not completely eliminated activity of 3HB release and indicated the presence of i-PHB depolymerase isoenzymes.


2012 ◽  
Vol 29 ◽  
pp. S66
Author(s):  
E.C. Francisco ◽  
E. Jacob-Lopes ◽  
T.T. Franco

2000 ◽  
Vol 66 (2) ◽  
pp. 783-787 ◽  
Author(s):  
Marisa K. Chelius ◽  
Eric W. Triplett

ABSTRACT The endophytic lifestyle of Klebsiella pneumoniae is described, including the production of dinitrogenase reductase by bacteria residing in maize root tissue. The green fluorescent protein (GFP) was used to detect the colonization of maize by K. pneumoniae strains 2028 and 342. These strains were found to reside in intercortical layers of the stem and within the region of maturation in the root. The production of dinitrogenase reductase by GFP-tagged bacteria was visualized using immunolocalization. This activity was only apparent when bacteria were supplied with an exogenous carbon source. The results suggest that maize provides a suitable habitat for K. pneumoniae and that this species is capable of producing nitrogenase under the appropriate plant cultivation conditions.


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