A simple plate test for the determination of protocatechuic acid utilization by soil bacteria

1968 ◽  
Vol 14 (1) ◽  
pp. 88-89 ◽  
Author(s):  
Veronica Sundman

The method described makes use of the color reaction between protocatechuic acid and ferric ions. Separately sterilized protocatechuic acid is added to soil extract agar before plates are poured. After suitable incubation the plates are flooded with ferric chloride solution. Colorless zones around growth contrasting with the green color of the protocatechuic acid containing agar indicate utilization of protocatechuic acid. With the aid of this method the frequency of strains that use protocatechuic acid, among random bacterial isolates of soil origin, was found to vary between 26 and 44% according to the soil investigated.


1992 ◽  
Vol 41 (3) ◽  
pp. T45-T47 ◽  
Author(s):  
Masanobu SAHARA ◽  
Hirotoshi YOSHIMURA ◽  
Fumio SAGARA ◽  
Keihei UFAO ◽  
Isao YOSHIDA ◽  
...  


1968 ◽  
Vol 17 (10) ◽  
pp. 1273-1278 ◽  
Author(s):  
Masayoshi EZAWA ◽  
Osamu MATSUZAKI


1977 ◽  
Vol 23 (5) ◽  
pp. 811-812 ◽  
Author(s):  
H Yatzidis

Abstract Total urinary protein is rapidly precipitated at room temperature by tannic acid. The tannic acid/protein precipitate, dissolved in aqueous triethanolamine/ferric chloride solution, gives a purple-violet color of high absorptivity. Absorbance at 510 nm is linearly related to concentration from 0.05 to 1.50 A for a protein content of 0.05 to 1.50 g/liter, and less than 5 mg/liter can be detected. The CV and analytical recovery ranged from 0.5 to 1.8% and 98 to 103%, respectively. Nonprotein urinary constituents do not interfere.



HortScience ◽  
1997 ◽  
Vol 32 (4) ◽  
pp. 735-736 ◽  
Author(s):  
Asma Ziauddin ◽  
Mingsheng Peng ◽  
David J. Wolyn

Clear visualization of asparagus (Asparagus officinalis L.) microspore nuclei with common stains such as acetocarmine or DAPI is difficult, hindering cytological analyses. The addition of saturated aqueous ferric chloride solution to Carnoy's I fixative (30 μL·mL-1) resulted in clear visualization of nuclei. A distinct nucleus was observed in uninucleate cells and the vegetative and generative nuclei were clearly visible in binucleate microspores. This method can be used reliably for determination of asparagus microspore developmental stage. Chemical name used: 4′,6-diamidino-2-phenylindole-2HCL (DAPI).



2013 ◽  
Vol 2 (1) ◽  
pp. 36-42 ◽  
Author(s):  
Evan Mitchell Lutton ◽  
Rosa Schellevis ◽  
Anupama Shanmuganathan

Soil bacteria comprise a largely untapped resource with only 1-10% of bacterial species predicted to live in soil being culturable in the laboratory. Establishing culture-dependent protocols that identify unique operational taxonomic units (OTUs) is an important research topic in soil bacterial ecology. The culturability of soil bacteria may be improved by employing different culture media due to inherent preferences of growth substrate utilization. Soil-extract agar, R-2A agar, and 1% nutrient agar were used in this study to isolate bacteria obtained from soil samples collected in winter months to increase the understanding of bacterial diversity in Abernathy Field Station, a Marcellus shale temperate forest in Washington, Pennsylvania. Changes in bacterial diversity can be used to assess the early impact of anthropological factors, such as hydraulic fracturing in the Marcellus shale region, which may lead to severe environmental problems. For the purpose of long term ecological monitoring, data obtained from this year’s sample collection were analyzed in conjunction with previous years’ assessments. Bacterial isolates were analyzed taxonomically and phylogenetically. Unique OTUs were identified through comparative analysis of 16S rDNA. The Shannon-Weaver and Simpson’s diversity indices ranked isolates on soil-extract agar highest for species richness, and rarefaction analysis suggests that sampling saturation of OTUs identified on soil-extract agar has not yet been reached. Each culture medium studied supported isolates of four common phyla: Actinobacteria, Bacteroidetes, Firmicutes, and Proteobacteria. Soil-extract agar supported the greatest proportion of pigmented colonies including a Cyanobacterium which exhibited intra-16S rDNA polymorphism. Each culture medium supported the growth of unique OTUs and genera with Bacillus, Flavobacterium, Pseudomonas, Rhizobium, and Streptomyces found on each. This study suggests that utilizing different culture media can increase the culturability of soil bacteria.



2007 ◽  
Vol 17 (2) ◽  
pp. 266-271 ◽  
Author(s):  
Eun-Joo Kum ◽  
Hee-Young Ryu ◽  
Gi-Seok Kwon ◽  
Ho-Yong Sohn


2020 ◽  
Vol 36 (4) ◽  
pp. 126-135
Author(s):  
T.V. Shushkova ◽  
D.O. Epiktetov ◽  
S.V. Tarlachkov ◽  
I.T. Ermakova ◽  
A.A. Leontievskii

The degradation of persistent organophosphorus pollutants have been studied in 6 soil bacterial isolates and in 3 bacterial strains adapted for utilization of glyphosate herbicide (GP) under laboratory conditions. Significant differences in the uptake of organophosphonates were found in taxonomically close strains possessing similar enzymatic pathways of catabolism of these compounds, which indicates the existence of unknown mechanisms of activity regulation of these enzymes. The effect of adaptation for GP utilization as a sole phosphorus source on assimilation rates of several other phosphonates was observed in studied bacteria. The newly found efficient stains provided up to 56% of GP decomposition after application to the soil in the laboratory. The unresolved problems of microbial GP metabolism and the trends for further research on the creation of reliable biologicals capable of decomposing organophosphonates in the environment are discussed. organophosphonates, glyphosate, biodegradation, bioremediation, C-P lyase, phosphonatase, degrading bacteria Investigation of phosphonatase and genome sequencing were supported by Russian Science Foundation Grant no. 18-074-00021.



RSC Advances ◽  
2021 ◽  
Vol 11 (28) ◽  
pp. 17283-17290
Author(s):  
Shuai Zhang ◽  
Cong Zhang ◽  
Xiaodong Shao ◽  
Rentian Guan ◽  
Yingying Hu ◽  
...  

A fluorometric method was proposed for the determination of Fe3+ and ascorbic acid (AA) based on blue and red dual fluorescence emissions of glutathione (GSH) stabilized-gold nanoclusters (AuNCs).



2009 ◽  
Vol 96 (4) ◽  
pp. 275-282 ◽  
Author(s):  
R. Dehghan ◽  
M. Noaparast ◽  
M. Kolahdoozan


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