Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “LEVULINIC ACID”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 487 records · Page 27Linked to original sources

The participation of the Shemin and C5 pathways in 5-aminolaevulinate and chlorophyll formation in higher plants and facultative photosynthetic bacteria.

Chlorophyll and bacteriochlorophyll formation from 14C-labelled precursors was studied during the illumination of etiolated maize leaves excised from dark-grown seedlings and in cell suspensions of respiring, dark-, aerobically-grown Rhodopseudomonas spheroides adapting to the photosynthetic state in the light under anaerobic conditions. It was found that 1-14C-labelled glutamate and 2-oxoglutarate were incorporated into the tetrapyrrole moieties of chlorophyll and bacteriochlorophyll. This suggests that the C5 pathway of tetrapyrrole biosynthesis operates in both Zea mays and R. spheroides since in the alternative Shemin pathway the label would have been lost as 14CO2 during the formation of succinyl-CoA prior to the condensation with glycine to form 5-aminolaevulinate. It was also found that 5(-14)C-labelled glutamate and 2-oxoglutarate were incorporated into these chlorophylls which is consistent with the operation of both the C5 and Shemin pathways. That the Shemin pathway is also involved was confirmed by the incorporation of [2(-14)C]glycine into both chlorophylls. None of these substrates were incorporated into the phytol moieties of either plant or bacterial chlorophyll or into the carotenoids. However, when [1(-14)C]acetate was added to greening maize leaves not only the tetrapyrrole and phytol moieties were labelled but also the carotenoids: the labelling of these lipids is consistent with their formation from acetate via the isopentenyl pyrophosphate pathway. By comparing the incorporation of [1(-14)C]2-oxoglutarate with that of [5(-14)C]2-oxoglutarate the approximate relative contribution of each pathway to chlorophyll biosynthesis was determined. In maize leaves both pathways contributed almost equally but in R. spheroides the contribution by the Shemin and C5 pathways was 90 and 10%, respectively.

Amino Acids↗

[Improved method for the determination of urinary delta-aminolevulinic acid in lead workers].

An improved method for the determination of urinary delta-aminolevulinic acid (ALA) as an indicator of lead absorption is described. It is a modification of the analytical procedure described by Tomokuni and Ogata in 1972. In the present method, the spot urine from lead-exposed workers which was diluted 3-fold with distilled water beforehand was used as the sample to eliminate as much as possible the urinary matrix interference. In addition, methyl acetoacetate was used as the condensation reagent for ALA-pyrrole, because the color intensity of ALA-pyrrole was higher with the use of methyl acetoacetate than that with ethyl acetoacetate which was used in the original method. The urinary ALA value determined by the present method was similar to that measured using an internal-standard addition method. This method is suitable as a rapid and inexpensive screening procedure for the routine quantitative analysis of urinary ALA.

Aminolevulinic Acid↗

Regulation of mitochondrial biogenesis: enzymatic changes in cytochrome-deficient yeast mutants requiring delta-aminolevulinic acid.

Yeast cells almost completely deficient in all cytochromes were obtained by introducing two defective nuclear genes, cyd1 and cyc4, into the same haploid strain. The action of the two mutant genes is synergistic, since either gene acting singly results in only partial cytochrome deficiency. Normal synthesis of all cytochromes can be restored in the double mutant by adding delta-aminolevulinic acid to the growth medium. The optimum concentration of delta-aminolevulinate for restoration of cytochrome synthesis is about 40 muM; when higher concentrations are used, synthesis of cytochromes is partially suppressed, particularly that of cytochrome a.a3. Growth yield of the double mutant is stimulated by ergosterol and Tween 80, a source of unsaturated fatty acid. Methionine stimulates further. None of these nutrients is required for growth when sufficient delta-aminolevulinic acid is present in the growth medium. With respect to nutritional responses, the single-gene, cytochrome-deficient mutant, ole3, behaves like the double mutant. The frequency of the p-mutation in the double mutant grown in the absence of ergosterol, Tween 80, and delta-aminolevulinic acid is at least 15%. The frequency can be reduced to less than 1% by either delta-aminolevulinic acid or Tween 80. Ergosterol alone does not decrease the p- frequency. The ole3 mutant does not exhibit increased p-frequency under similar conditions of unsaturated fatty acid deficiency.

5-Aminolevulinate Synthetase↗

[Evaluation of porphyrinogenic effect of lindane in rats].

In order to study the porphyrinogenic ability of lindane in mammals, rats were treated with the pesticide suspended with the aid of Tween or dissolved in oil during about 3 months. The urinary excretion of porphyrins and its precursors: delta-aminolaevulinate (ALA) and porphobilinogen (PBG), as well as the faecal excretion of coproporphyrin (COPRO) and protoporphyrin (PROTO) was determined weekly. At the end of the treatment the hepatic activities of ALA Synthase (ALA-S), the first and rate limiting enzyme of haem pathway, and porphyrinogen carboxy-lyase (PCL), enzyme which sequentially decarboxylates uroporphyrinogen (8 COOH) to coproporphyrinogen (4 COOH), were assayed. Lindane moderately increased the urinary excretion of porphyrins and its precursors, being the former the mainly affected parameter. The faecal excretion of COPRO and PROTO was also increased. However, the hepatic activity of ALA-S was not altered. This would suggest that the regulatory haem pool was not affected. Nor was PCL activity altered in spite of being the key enzyme for the attack of other chlorinated compounds. Although hexachlorobenzene (HCB), a very well known porphyrinogenic drug, and lindane are chemically related and generate similar metabolites, the last one produces a small and qualitatively different alteration of haem biosynthesis. This may be related with the absence or scarce formation of the reactive metabolite that accounts for the porphyrinogenic ability of HCB.

5-Aminolevulinate Synthetase↗

Simple screening test for qualitative detection of increased delta-aminolevulinic acid in urine.

A simple qualitative procedure for demonstrating increased delta-aminolevulinic acid (ALA) in urine is needed to identify individuals with an inherited deficiency of the enzyme ALA dehydratase, a newly described porphyria-like syndrome. The present procedure includes two steps, the last of which is carried out only on samples that are positive in the first step. Urine is tested for pyrroles, preformed or formed by heating with acetylacetone, by looking for a pink color after p-dimethylaminobenzaldehyde is added. Samples showing the color are next tested for ALA by adsorbing natural pyrroles onto Dowex-1 in sodium acetate, heating the supernate with acetylacetone, adsorbing the resulting aminoketone pyrroles onto Dowex-1 in water, separating the ALA from other aminoketones by differential extraction, and again looking for a pink color with p-dimethylaminobenzaldehyde. Positive urines, those with concentrations of ALA greater than or equal to 10-15 mg/L, yield a pink color in each step. Samples with greater than 30 mg/L ALA show a magenta color. Aminoacetone in excess of 3 mg/L ALA also yields a pink color, but such a concentration in urine is unlikely. Many samples can easily be tested concurrently.

Acute Disease↗

Statistical analysis of urinary delta-aminolevulinic acid (ALAU) excretion in the white-footed mouse associated with lead smelting.

ALAU in white-footed mice trapped in the vicinity of a lead smelter has been measured to study the biological effect of lead smelting operations and the rate at which the ALAU level diminishes after removing animals from contaminated environments. The statistical method which has been developed for this purpose shows that the ALAU levels are initially higher among animals near the smelter and diminish to a common level after 5-6 weeks. The statistical method is generally applicable to a variety of physiological functions which exhibit a decay curve with respect to time.

Aminolevulinic Acid↗