A simple screening method for isovaleric acid production by Propionibacterium freudenreichii in Swiss cheese

2004 ◽  
Vol 14 (8) ◽  
pp. 697-700 ◽  
Author(s):  
Anne Thierry ◽  
Romain Richoux ◽  
Jean-René Kerjean ◽  
Sylvie Lortal
2004 ◽  
Vol 14 (9) ◽  
pp. 801-807 ◽  
Author(s):  
Anne Thierry ◽  
Romain Richoux ◽  
Jean-René Kerjean

1970 ◽  
Vol 16 (5) ◽  
pp. 420-422 ◽  
Author(s):  
Toshiyuki Ando ◽  
William L Nyhan

Abstract Isovaleric acidemia is one of an enlarging group of inherited metabolic diseases now recognized to cause death in the neonatal period. Rapid, simple detection is essential for diagnosis of these conditions. We describe a method that fulfills these criteria for isovaleric acidemia. Excretion of isovalerylglycine in the urine more reliably indicates the condition than the presence of volatile isovaleric acid in the blood. Isovalerylglycine is extracted from urine and separated by thin-layer chromatography from other constituents of urine. It is detected by spraying the chromatogram with bromcresol purple. Isovalerylglycine does not appear in normal urine.


2002 ◽  
Vol 68 (2) ◽  
pp. 608-615 ◽  
Author(s):  
Anne Thierry ◽  
Marie-Bernadette Maillard ◽  
Mireille Yvon

ABSTRACT Several branched-chain volatile compounds are involved in the flavor of Swiss cheese. These compounds are probably produced by enzymatic conversion of branched-chain amino acids, but the flora and the pathways involved remain hypothetical. Our aim was to determine the ability of Propionibacterium freudenreichii, which is one of the main components of the secondary flora of Swiss cheese, to produce flavor compounds during leucine catabolism. Cell extracts and resting cells of two strains were incubated in the presence of l-leucine, α-ketoglutaric acid, and cofactors, and the metabolites produced were determined by high-performance liquid chromatography and gas chromatography. The first step of leucine catabolism was a transamination that produced α-ketoisocaproic acid, which was enzymatically converted to isovaleric acid. Both reactions were faster at pH 8.0 than at acidic pHs. Cell extracts catalyzed only the transamination step under our experimental conditions. Small amounts of 3-methylbutanol were also produced by resting cells, but neither 3-methylbutanal norα-hydroxyisocaproic acid was detected. l-Isoleucine and l-valine were also converted to the corresponding acids and alcohols. Isovaleric acid was produced by both strains during growth in a complex medium, even under conditions simulating Swiss cheese conditions (2.1% NaCl, pH 5.4, 24�C). Our results show that P. frendenreichii could play a significant role in the formation of isovaleric acid during ripening.


PEDIATRICS ◽  
1959 ◽  
Vol 23 (4) ◽  
pp. 731-737
Author(s):  
Louis Gluck

A simple patch test, designed as a screening test for cystic fibrosis of the pancreas, is reported in preliminary form. In trials carried out with 207 patients it has proved accurate and reliable. A brief resume of the physiology of sweating, especially as pertinent to diagnostic methods in pediatrics, is also presented. Studies are in progress aiming toward further refinement of this method.


2018 ◽  
Vol 125 (2) ◽  
pp. 480-489 ◽  
Author(s):  
F.D.S. Belgrano ◽  
B.R.F. Verçoza ◽  
J.C.F. Rodrigues ◽  
R. Hatti‐Kaul ◽  
N. Pereira

Author(s):  
Carlos Fernando Odir Rodrigues Melo ◽  
Luiz Claudio Navarro ◽  
Diogo Noin de Oliveira ◽  
Tatiane Melina Guerreiro ◽  
Estela de Oliveira Lima ◽  
...  

1970 ◽  
Vol 16 (6) ◽  
pp. 421-425 ◽  
Author(s):  
C. Wayne Moss ◽  
R. T. Howell ◽  
D. C. Farshy ◽  
V. R. Dowell ◽  
J. B. Brooks

The proteolytic activity and volatile fatty acid production of 10 isolates of Clostridium botulinum type F from diverse geographical locations were determined. Two of the 10 strains were non-proteolytic, 3 were slightly proteolytic, and 5 were strongly proteolytic. The non-proteolytic cultures and the slightly proteolytic cultures produced acetic and butyric acid. The strongly proteolytic cultures produced mainly acetic, butyric, isobutyric, and isovaleric acid, and small to trace amounts of propionic, isocaproic, and caproic acid. The relative amounts of the various acids produced were markedly influenced by the growth medium. The addition of glucose to the growth medium caused an increase in the relative amount of butyric acid and a decrease in isobutyric and isovaleric acid.


2000 ◽  
Vol 46 (4) ◽  
pp. 325-332 ◽  
Author(s):  
Sanae Kato ◽  
Isao Yumoto

To examine the distribution of the Na+-translocating NADH-quinone reductase (Na+-NQR) among marine bacteria, we developed a simple screening method for the detection of this enzyme. By reference to the homologous sequences of the Na+-NQR operons from Vibrio alginolyticus and Haemophilus influenzae, a pair of primers was designed for amplification of a part of the sixth ORF (nqr6) of the Na+-NQR operon. When PCR was performed using genomic DNA from 13 marine bacteria, a 0.9-kbp fragment corresponding to nqr6 was amplified in 10 strains. Although there were three PCR-negative strains phylogenetically, based on the sequence of the 16S rRNA, these were placed far from the PCR-positive strains. No product was observed in the case of nonmarine bacteria. The nucleotide and predicted amino acid sequences of nqr6 were highly conserved among the PCR-positive marine bacteria. A phylogenetic analysis of marine bacteria, based on nqr6 sequencing, was performed.Key words: Na+-translocating, NADH-quinone reductase, marine bacteria, PCR.


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