Glyconeogenesis, Krebs Cycle Intermediates and Enzymes during Embryogenesis of the Camel Tick, Hyalomma dromedarii (Acarina: Ixodidae)

1990 ◽  
Vol 15 (1) ◽  
pp. 11-23 ◽  
Author(s):  
Ragaa R. Hamed ◽  
Afaf S. Fahmy ◽  
Mamdouh Y. Kamel
2011 ◽  
Vol 77 (24) ◽  
pp. 8754-8764 ◽  
Author(s):  
Karolien Bers ◽  
Baptiste Leroy ◽  
Philip Breugelmans ◽  
Pieter Albers ◽  
Rob Lavigne ◽  
...  

ABSTRACTThe soil bacterial isolateVariovoraxsp. strain SRS16 mineralizes the phenylurea herbicide linuron. The proposed pathway initiates with hydrolysis of linuron to 3,4-dichloroaniline (DCA) andN,O-dimethylhydroxylamine, followed by conversion of DCA to Krebs cycle intermediates. Differential proteomic analysis showed a linuron-dependent upregulation of several enzymes that fit into this pathway, including an amidase (LibA), a multicomponent chloroaniline dioxygenase, and enzymes associated with a modified chlorocatecholortho-cleavage pathway. Purified LibA is a monomeric linuron hydrolase of ∼55 kDa with aKmand aVmaxfor linuron of 5.8 μM and 0.16 nmol min−1, respectively. This novel member of the amidase signature family is unrelated to phenylurea-hydrolyzing enzymes from Gram-positive bacteria and lacks activity toward other tested phenylurea herbicides. Orthologues oflibAare present in all other tested linuron-degradingVariovoraxstrains with the exception ofVariovoraxstrains WDL1 and PBS-H4, suggesting divergent evolution of the linuron catabolic pathway in differentVariovoraxstrains. The organization of the linuron degradation genes identified in the draft SRS16 genome sequence indicates that gene patchwork assembly is at the origin of the pathway. Transcription analysis suggests that a catabolic intermediate, rather than linuron itself, acts as effector in activation of the pathway. Our study provides the first report on the genetic organization of a bacterial pathway for complete mineralization of a phenylurea herbicide and the first report on a linuron hydrolase in Gram-negative bacteria.


1954 ◽  
Vol 142 (907) ◽  
pp. 155-160 ◽  

The presence of a large central vacuole in plant cells has greatly hindered histochemical and biochemical investigations, because, when a homogenate is prepared, the vacuolar sap, which frequently includes large quantities of the substrate and product of an enzyme reaction and in certain cases enzyme inhibitors, becomes intimately mixed with the somewhat limited amount of protoplasm present. Bentley (1952), for instance, has shown that malonic acid is widely distributed in plants; fluoroacetic acid occurs in Dichapetalum cymosum (Marais 1944), and transaconitic acid may be present in certain members of the Ranunculaceae. Though these facts pose interesting problems in the permeability relations of cell components, they greatly complicate the analysis of homogenates. Dialysis provides one method of isolating active enzyme material from the homogenate, but the concomitant loss of cofactors has limited its application. A partial solution to the problem has been obtained by isolating particulate material by differential centrifugation. This method has made possible investigations of metabolism not amenable to study by the classical methods of enzymology and simultaneously has provided an approach to the study of the spatial relations of enzymes. The pioneer work was performed by Hill & Bhagvat (1939), who demonstrated the association of cytochrome oxidase with particulate material. Several workers (Meeuse 1950; Bhagvat & Hill 1951; Stafford 1951) have demonstrated the association of succinoxidase with particulate material isolated from homogenates prepared in dilute phosphate buffer, but cytochrome c was necessary for activity. Meeuse (1950) also found that malic oxidase was associated with particulate material, but DPN and cytochrome c were required for activity. Millerd, Bonner, Axelrod & Bandurski (1951), Stafford (1953), Price & Thimann (1953) and Davies (1953) have isolated particulate material from seedlings which was active in the oxidation of Krebs-cycle intermediates. Millerd et al . (1951) were also able to demonstrate that phosphorylation accompanied the oxidation of Krebs-cycle intermediates.


2020 ◽  
Vol 80 (3) ◽  
pp. 349-361
Author(s):  
Hassan M. M. Masoud ◽  
Mohamed S. Helmy ◽  
Doaa A. Darwish ◽  
Mohamed M. Abdel-Monsef ◽  
Mahmoud A. Ibrahim

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