scholarly journals Formaldehyde as an oxidation product of chlorophyll extracts

Of recent years the action on carbon dioxide of chlorophyll in vitro has assumed some importance as possibly throwing light on the nature of the photo-synthetic process of green plants. Thus Usher and Priestley have stated that films of extracted chlorophyll in the presence of moist air and carbon dioxide produce formaldehyde and hydrogen peroxide under the influence of light. The earlier work of these authors has been adversely commented upon by several writers, notably by Ewart, to whose criticisms Usher and Priestley have replied with a number of additional experiments and arguments, referring also to the work of Schryver, subsequent to that of Ewart, as affording strong confirmation of their views as far as the synthesis of the aldehyde is concerned. The facts set forth in the present paper came to light during an attempt to confirm and extend the observations of Usher and Priestley and of Schryver. Grass was extracted with alcohol, usually in the cold and in the presence of calcium carbonate. In some experiments the alcoholic liquid was evaporated to dryness under reduced pressure and the residue extracted with ether; in others a solution of chlorophyll in light petroleum was obtained by shaking the alcoholic solution with that liquid. The method of experiment was based upon that described by Schryver, the ether or petroleum extract being allowed to evaporate on glass plates and exposed to light under the various conditions to be mentioned below. As was the case in the later experiments of Usher and Priestley themselves, the test which has been relied upon for the detection of formaldehyde is the very delicate one devised by Schryver, who has found that the reaction is not given by such other members of the series as have been examined up to the present. It has been assumed in the course of these experiments, as in the work of the investigators already mentioned, that the aldehyde produced is formaldehyde, but it is very important that the possibility of the observed effects being due to some other aldehyde or to a mixture of aldehydes should be borne in mind. This point still requires investigation.

In a previous paper* it was shown that carbon dioxide is decomposed in the green parts of plants independently of vital or enzymic activity, formaldehyde and hydrogen peroxide being produced. It follows from the analysis of the process of carbon assimilation there set out that this first step, the photolysis of carbon dioxide, should be capable of being artificially induced under laboratory conditions. It is impossible here to give a brief account of the work of previous investigators on these lines; it is sufficient to state that all experiments with chlorophyll solutions have given negative results, and as regards those with other forms of chlorophyll, such as dried powdered leaves or expressed juice, the balance of evidence favours the view that to decomposition takes place. Reference may be made to papers by Friedel and Macchiati on the positive side, and by Harroy,§ Herzog,|| and, quite recently, Bernard,¶ who obtained only negative results. Experiments with uranium compounds will be considered later.


This trial research was performed to discuss the immune-influence of Melaleuca leucadendra ‘paper-bark tree’ dried leaves which is an important medical plant known in many regions in the world. The leaves were dissolved in a mixture of (ethanol + water) (3:1) mixture, then filtered, evaporated and dried under reduced pressure to obtain leaves extract. The macrophages of blood derived origin were provided from rats and mixed with three different leaves extracts doses in tissue culture plates and incubated then stained with fluorescent acridine orange and examined under fluorescent microscope to assess the phagocytic and killing potency. The wells contents were aspirated and assayed for nitric oxide and interleukin-2 levels. The results displayed an obvious increase in phagocytic, killing performance as well as nitric oxide and IL-2 level production than control in a dose dependent manner. The obtained results suggested the immune-stimulant impact of the paper-bark tree leaves.


2015 ◽  
Vol 197 (14) ◽  
pp. 2383-2391 ◽  
Author(s):  
Semen A. Leyn ◽  
Irina A. Rodionova ◽  
Xiaoqing Li ◽  
Dmitry A. Rodionov

ABSTRACTAutotrophic microorganisms are able to utilize carbon dioxide as their only carbon source, or, alternatively, many of them can grow heterotrophically on organics. Different variants of autotrophic pathways have been identified in various lineages of the phylumCrenarchaeota. Aerobic members of the orderSulfolobalesutilize the hydroxypropionate-hydroxybutyrate cycle (HHC) to fix inorganic carbon, whereas anaerobicThermoprotealesuse the dicarboxylate-hydroxybutyrate cycle (DHC). Knowledge of transcriptional regulation of autotrophic pathways inArchaeais limited. We applied a comparative genomics approach to predict novel autotrophic regulons in theCrenarchaeota. We report identification of two novel DNA motifs associated with the autotrophic pathway genes in theSulfolobales(HHC box) andThermoproteales(DHC box). Based on genome context evidence, the HHC box regulon was attributed to a novel transcription factor from the TrmB family named HhcR. Orthologs of HhcR are present in allSulfolobalesgenomes but were not found in other lineages. A predicted HHC box regulatory motif was confirmed byin vitrobinding assays with the recombinant HhcR protein fromMetallosphaera yellowstonensis. For the DHC box regulon, we assigned a different potential regulator, named DhcR, which is restricted to the orderThermoproteales. DhcR inThermoproteus neutrophilus(Tneu_0751) was previously identified as a DNA-binding protein with high affinity for the promoter regions of two autotrophic operons. The global HhcR and DhcR regulons reconstructed by comparative genomics were reconciled with available omics data inMetallosphaeraandThermoproteusspp. The identified regulons constitute two novel mechanisms for transcriptional control of autotrophic pathways in theCrenarchaeota.IMPORTANCELittle is known about transcriptional regulation of carbon dioxide fixation pathways inArchaea. We previously applied the comparative genomics approach for reconstruction of DtxR family regulons in diverse lineages ofArchaea. Here, we utilize similar computational approaches to identify novel regulatory motifs for genes that are autotrophically induced in microorganisms from two lineages ofCrenarchaeotaand to reconstruct the respective regulons. The predicted novel regulons in archaeal genomes control the majority of autotrophic pathway genes and also other carbon and energy metabolism genes. The HhcR regulon was experimentally validated by DNA-binding assays inMetallosphaeraspp. Novel regulons described for the first time in this work provide a basis for understanding the mechanisms of transcriptional regulation of autotrophic pathways inArchaea.


Odontology ◽  
2021 ◽  
Author(s):  
Sarita Giri ◽  
Ayuko Takada ◽  
Durga Paudel ◽  
Koki Yoshida ◽  
Masae Furukawa ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Vishal Panchariya ◽  
Vishal Bhati ◽  
Harishkumar Madhyastha ◽  
Radha Madhyastha ◽  
Jagdish Prasad ◽  
...  

AbstractExtraction of biosurfactants from plants is advantageous than from microbes. The properties and robustness of biosurfactant derived from the mesocarp of Balanites aegyptiaca have been reported. However, the dark brown property of biosurfactant and lack of knowledge of its biocompatibility limits its scope. In the present work, the decolorization protocol for this biosurfactant was optimized using hydrogen peroxide. The hemolytic potential and biocompatibility based on cell toxicity and proliferation were also investigated. This study is the first report on the decolorization and toxicity assay of this biosurfactant. For decolorization of biosurfactant, 34 full factorial design was used, and the data were subjected to ANOVA. Results indicate that 1.5% of hydrogen peroxide can decolorize the biosurfactant most efficiently at 40 °C in 70 min at pH 7. Mitochondrial reductase (MTT) and reactive oxygen species (ROS) assays on M5S mouse skin fibroblast cells revealed that decolorized biosurfactant up to 50 µg/mL for 6 h had no significant toxic effect. Hemolysis assay showed ~ 2.5% hemolysis of human RBCs, indicating the nontoxic effect of this biosurfactant. The present work established a decolorization protocol making the biosurfactant chromatically acceptable. Biocompatibility assays confirm its safer use as observed by experiments on M5S skin fibroblast cells under in vitro conditions.


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