Isolation and Characterization of (+)-1,1a-Dihydroxy-1-hydrofluoren-9-one Formed by Angular Dioxygenation in the Bacterial Catabolism of Fluorene

1993 ◽  
Vol 193 (1) ◽  
pp. 67-76 ◽  
Author(s):  
S.A. Selifonov ◽  
M. Grifoll ◽  
J.E. Gurst ◽  
P.J. Chapman
1998 ◽  
Vol 44 (8) ◽  
pp. 734-742
Author(s):  
Mercè Casellas ◽  
Magdalena Grifoll ◽  
Jordi Sabaté ◽  
Anna Maria Solanas

Pseudomonas mendocina MC2, able to use 9-fluorenone but not fluorene as its sole source of carbon and energy, was isolated. Identification of metabolites in growth media and washed cell suspensions indicated that strain MC2 metabolizes 9-fluorenone via angular dioxygenation of the ketone, to give 1,1a-dihydroxy-1-hydro-9-fluorenone, followed by the opening of the five-membered ring and further degradation of the resulting biphenyl derivative by reactions akin to those of biphenyl metabolism, which produce phthalate as an intermediate. The aim of this research was to study the biodegradation of fluorene by a co-culture of strain MC2 and Arthrobacter sp.strain F101, which grows on fluorene and simultaneously transforms a fraction of the substrate to 9-fluorenone, which accumulates as a dead-end product. Growing with 0.1 g fluorene/L, Arthrobacter sp. strain F101 caused the total removal of this compound from the cultures, but when this strain was grown with 1g fluorene/L, only 16% of the fluorene was used. The addition of 9-fluorenone to cultures growing on fluorene showed that 9-fluorenone inhibits fluorene degradation. Finally, when Pseudomonas mendocina MC2 and Arthrobacter sp. strain F101 were co-cultured with 1g fluorene/L as a sole source of carbon and energy, the growth of the strains completely removed fluorene in 2 days. 9-Fluorenone did not accumulate and the carbon assimilation into cell biomass was estimated as approximately 46%. Key words: microbial consortium, fluorene, 9-fluorenone, biodegradation.


2000 ◽  
Vol 31 (2) ◽  
pp. 149-149 ◽  
Author(s):  
T Tozaki ◽  
H Kakoi ◽  
S Mashima ◽  
K Hirota ◽  
T Hasegawa ◽  
...  

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
B Tóth ◽  
N Kúsz ◽  
A Csorba ◽  
T Kurtán ◽  
J Hohmann ◽  
...  

2017 ◽  
Author(s):  
L Passolt ◽  
A Jindaprasert ◽  
T Le Tran ◽  
R Seupel ◽  
G Bringmann ◽  
...  

1974 ◽  
Vol 31 (01) ◽  
pp. 072-085 ◽  
Author(s):  
M Kopitar ◽  
M Stegnar ◽  
B Accetto ◽  
D Lebez

SummaryPlasminogen activator was isolated from disrupted pig leucocytes by the aid of DEAE chromatography, gel filtration on Sephadex G-100 and final purification on CM cellulose, or by preparative gel electrophoresis.Isolated plasminogen activator corresponds No. 3 band of the starting sample of leucocyte cells (that is composed from 10 gel electrophoretic bands).pH optimum was found to be in pH range 8.0–8.5 and the highest pH stability is between pH range 5.0–8.0.Inhibition studies of isolated plasminogen activator were performed with EACA, AMCHA, PAMBA and Trasylol, using Anson and Astrup method. By Astrup method 100% inhibition was found with EACA and Trasylol and 30% with AMCHA. PAMBA gave 60% inhibition already at concentration 10–3 M/ml. Molecular weight of plasminogen activator was determined by gel filtration on Sephadex G-100. The value obtained from 4 different samples was found to be 28000–30500.


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