scholarly journals Angelicin as the Principal Allelochemical in Heracleum sosnowskyi Fruit

2015 ◽  
Vol 10 (5) ◽  
pp. 1934578X1501000 ◽  
Author(s):  
Maryia Mishyna ◽  
Nikolai Laman ◽  
Valery Prokhorov ◽  
Yoshiharu Fujii
Keyword(s):  
Inhibitory Activity ◽  
Specific Activity ◽  
Lolium Multiflorum ◽  
Distribution Patterns ◽  
Total Activity ◽  
Cold Stratification ◽  
Hypocotyl Growth ◽  
Heracleum Sosnowskyi ◽  
Crude Extracts ◽  
Inhibitory Potential

Distribution patterns of furocoumarins in fruits of the invasive species Heracleum sosnowskyi Manden. (Sosnowskyi's hogweed) during a cold stratification period were investigated. Angelicin, bergapten, methoxalen and imperatorin were mainly localized in the fruit coats and their content varied depending on the fruit source. Cold stratification treatment (90 days, 2–3°C) reduced the content of furocoumarins in the fruit coats by more than two times, compared with those before stratification. The specific activity of the detected furocoumarins and total activity of crude extracts were evaluated using Lactuca sativa, as acceptor plant. Crude extracts obtained from fruit coats and seeds of H. sosnowskyi suppressed 50% of radicle and hypocotyl growth of lettuce seedlings at the concentration range of 1.0–1.7 mg/mL. The inhibitory activity of angelicin was proved to be the highest compared with the other tested furocoumarins, and the inhibitory activity of crude extracts could be explained mainly by the presence of angelicin. Both, monocots ( Lolium multiflorum, Phleum pratensis, Festuca pratesis, Lolium perenne) and dicots ( Tripholium repens, Trifolium pretense) were found to be sensitive to the exudates of whole H. sosnowskyi fruits. Thus, we assume, that high inhibitory potential of furocoumarins, especially angelicin, at high seed productivity of H. sosnowskyi might have an ecological significance in plant-plant interaction.

scholarly journals Caffeine: The Allelochemical Responsible for the Plant Growth Inhibitory Activity of Vietnamese Tea (Camellia sinensis L. Kuntze)

Agronomy ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 396 ◽  
Author(s):  
Van Thi Thanh PHAM ◽  
Tamer ISMAIL ◽  
Maryia MISHYNA ◽  
Kwame Sarpong APPIAH ◽  
Yosei OIKAWA ◽  
...  
Keyword(s):  
Green Tea ◽  
Weed Management ◽  
Inhibitory Activity ◽  
High Performance ◽  
Specific Activity ◽  
Total Activity ◽  
Inhibitory Effect ◽  
Hypocotyl Growth ◽  
Radicle Growth ◽  
Growth Inhibitory Activity

The present study aimed to examine the phytotoxic potential of seven Vietnamese tea samples based on the specific and total activity of caffeine and tea extracts on test plants. The sandwich method results indicated that the inhibitory effect of tea samples on the radicle and hypocotyl growth of lettuce seedlings was dependent on the concentration and type of tea samples, and also the presence of agar soluble allelochemicals. Among the seven tea samples, the leachates from Vinatea-green tea showed the highest inhibition on the radicle growth of lettuce seedlings with 50% suppression at 0.12 mg dry leaves/mL of agar. Caffeine concentration in tea samples analyzed by high-performance liquid chromatography (HPLC) varied from 20.7 to 38.2 µg/mL of dry leaves. The specific activity (EC50 value) of pure caffeine was 75 µg/mL, and the highest total activity of caffeine estimated in Vinatea-green tea was 0.51 [no unit]. Caffeine from green and oolong tea may be considered as one of the contributors to the inhibitory activity of the crude extract. Moreover, the phytotoxicity of pure caffeine and aqueous tea extracts was highly selective on the growth of different plant species. The concentration of caffeine detected from tea farm soil ranged from 0.137 to 0.145 µg/g soil. The results indicated that caffeine might be considered as a promising allelochemical from Vietnamese tea and can be a good candidate for weed management.

scholarly journals Characterization of Genetically Engineered Linamarase (β-glucosidase) from Saccharomyces cerevisiae

2013 ◽  
Vol 1 (2) ◽  
pp. 139-145
Author(s):  
Julius harIkya ◽  
Charles Charles ◽  
James Ayatse
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Specific Activity ◽  
Methyl Cellulose ◽  
Total Activity ◽  
Genetically Engineered ◽  
Chromosomal Dna ◽  
Ph Tolerance ◽  
Crude Extracts ◽  
Sulphur Amino Acids

The characterization parameters of genetically engineered linamarase (β-glucosidase) from Saccharomyces cerevisiae due to action of the enzyme on linamarin as influenced by degree of purification, pH and temperature were investigated. Commercial native linamarase (CNLIN) was used as control. Linamarase genes (chromosomal DNA) and plasmids (circular DNA) isolated from bitter cassava and yeast respectively were restricted and ligated to produce recombinant genes (r-DNA). The r-DNA were introduced into the nucleus of CaCl2 induced competent Saccharomyces cerevisiae cells which transformed into strains capable of producing genetically engineered linamarase (GELIN). Recombinant S. cerevisiae cells at the stationary phase of growth were recovered, homogenized and centrifuged to obtain crude extracts designated as GELIN0. Carboxy methyl cellulose, diethyl amino-ethyl-sephadex and diethyl amino-ethyl-cellulose were used to purify the crude extracts resulting in GELIN1, GELIN2 and GELIN3, respectively. The physical characterization parameters of the enzyme extracts such as impurity levels, molecular weights (Mwt), number of isoenzyme, sulphur amino acids (methionine and cysteine) and the electrical charges were evaluated using standard methods. The ability of the enzyme extracts and a commercial native linamarase (CNLIN) to hydrolyse cyanogenic glucosides was challenged using linamarin (cassava) as substrates for characterization of activity kinetic profiles such as optimum pH (pHopt), temperature (Topt), total activity, specific activity, purity fold, yield and efficiency ratio. The results indicated that the genetically engineered linamarase(β-glucosidase) consisted of 3 isoenzyme forms. Purification conferred different ionic charges of zero to GELIN0, unit positive charge GELIN1, and unit negative charge to GELIN2 and GELIN3 respectively. Ranges for other parameters were Mwt (22,000-26,000 Daltons), insoluble protein impurity (0.4 -3.5 mg/100g sample) and purity fold (11.5 -1.0) for GELIN3 - GELIN0). Methionine and cystiene varied from 2.0 to 2.6% and 3.0 to 20% respectively (CNLIN - GELIN3). The native commercial enzyme (CNLIN) acted only at pH 6.8 on linamarin with pHopt and Topt of 6.8 and 35 oC respectively. The wide pH tolerance and specific activity towards linamarin degradation suggest a possible use of the genetically engineered linamarase from S. cerevisiae in detoxification of cassava for increased production exportation of cassava-based food products.

scholarly journals Involvement of Carnosic Acid in the Phytotoxicity of Rosmarinus officinalis Leaves

Toxins ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 498 ◽  
Author(s):  
Kwame Appiah ◽  
Hossein Mardani ◽  
Richard Omari ◽  
Vincent Eziah ◽  
John Ofosu-Anim ◽  
...  
Keyword(s):  
Specific Activity ◽  
Control Measure ◽  
High Specific Activity ◽  
Total Activity ◽  
Inhibitory Effect ◽  
Rosmarinus Officinalis ◽  
Carnosic Acid ◽  
High Concentration ◽  
Crude Extracts ◽  
Test Plants

Weeds are rapidly developing resistance to synthetic herbicides, and this can pose a threat to the ecosystem. Exploring allelopathic species as an alternative weed control measure can help minimize the ecological threat posed by herbicide-resistant weeds. In this study, we aimed to evaluate the contribution of some polyphenols to the allelopathy of rosemary (Rosmarinus officinalis L.). The phytotoxic effects of rosemary (leaves, roots, inflorescences, and stems) crude extracts were tested on lettuce (Lactuca sativa L.). Soils incorporated with dried rosemary leaves were also tested on test plants. Reversed-phase high-performance liquid chromatography (HPLC) analysis was used to determine the content of some polyphenols (caffeic, ferulic, gallic, rosmarinic, carnosic, and chlorogenic acids) in rosemary. The specific activity and total activity of crude extracts and individual compounds were evaluated using lettuce. The crude extract of rosemary leaves showed the highest growth inhibitory effect among the rosemary organs tested. Soil amended with rosemary leaf debris reduced the dry matter and seed emergence of lettuce. Carnosic acid was the main compound detected in rosemary leaves and had a high specific activity when tested on lettuce. During the seed germination period, there was observed filter paper coloration among the test plants treated with carnosic acid (250 μg/mL). The high concentration and strong inhibitory effect of carnosic acid could explain the inhibitory activity of the rosemary leaf extract. Hence, we conclude based on the total activity estimation that carnosic acid among the other tested compounds is the major allelochemical in rosemary leaves.

2,4-Dichloro-5-[(N-aryl/alkyl)sulfamoyl]benzoic Acid Derivatives: In Vitro Antidiabetic Activity, Molecular Modeling and In silico ADMET Screening

2019 ◽  
Vol 15 (2) ◽  
pp. 186-195 ◽  
Author(s):  
Samridhi Thakral ◽  
Vikramjeet Singh
Keyword(s):  
Molecular Docking ◽  
Benzoic Acid ◽  
Inhibitory Activity ◽  
In Silico ◽  
Computational Study ◽  
Antidiabetic Activity ◽  
Standard Drug ◽  
Benzoic Acid Derivatives ◽  
In Silico Admet ◽  
Inhibitory Potential

Background: Postprandial hyperglycemia can be reduced by inhibiting major carbohydrate hydrolyzing enzymes, such as α-glucosidase and α-amylase which is an effective approach in both preventing and treating diabetes. Objective: The aim of this study was to synthesize a series of 2,4-dichloro-5-[(N-aryl/alkyl)sulfamoyl] benzoic acid derivatives and evaluate α-glucosidase and α-amylase inhibitory activity along with molecular docking and in silico ADMET property analysis. Method: Chlorosulfonation of 2,4-dichloro benzoic acid followed by reaction with corresponding anilines/amines yielded 2,4-dichloro-5-[(N-aryl/alkyl)sulfamoyl]benzoic acid derivatives. For evaluating their antidiabetic potential α-glucosidase and α-amylase inhibitory assays were carried out. In silico molecular docking studies of these compounds were performed with respect to these enzymes and a computational study was also carried out to predict the drug-likeness and ADMET properties of the title compounds. Results: Compound 3c (2,4-dichloro-5-[(2-nitrophenyl)sulfamoyl]benzoic acid) was found to be highly active having 3 fold inhibitory potential against α-amylase and 5 times inhibitory activity against α-glucosidase in comparison to standard drug acarbose. Conclusion: Most of the synthesized compounds were highly potent or equipotent to standard drug acarbose for inhibitory potential against α-glucosidase and α-amylase enzyme and hence this may indicate their antidiabetic activity. The docking study revealed that these compounds interact with active site of enzyme through hydrogen bonding and different pi interactions.

5α-Reductase activity in stroma and epithelium of rat prostate and epididymis. A contribution to elucidation of the mechanism for development of hyperplastic growth of prostatic tissue

1983 ◽  
Vol 103 (2) ◽  
pp. 273-281 ◽  
Author(s):  
Ole Djøseland ◽  
Nicholas Bruchovsky ◽  
Paul S. Rennie ◽  
Navdeep Otal ◽  
Sian Høglo
Keyword(s):  
Enzyme Activity ◽  
Specific Activity ◽  
Reductase Activity ◽  
Major Change ◽  
Growth Stimulation ◽  
Total Activity ◽  
Prostatic Tissue ◽  
Ventral Prostate ◽  
Total Enzyme Activity ◽  
Abnormal Growth

Abstract. The 5α-reductase activity was assayed in homogenates of stroma and epithelium in the rat ventral prostate and epididymis. Samples consisting of 0.3 mg/ml tissue protein in TES buffer, pH 7.0 were incubated at 37°C for 30 min in the presence of 50 nm [1,2-3H]testosterone and a NADPH-generating system started with 5 × 10−4 m NADP. The yield of 5α-reduced metabolites, as established by using thin-layer chromatography, gave an estimate of enzyme activity. Whereas the specific activity of 5α-reductase was highest in prostatic stroma and epididymal epithelium, most of the total enzyme activity was associated with the epithelium in both the prostate and epididymis. The effect of dihydrotestosterone on specific activity of 5α-reductase was studied by administering the hormone to 7-day castrated rats. In prostate, the specific activity of both stromal and epithelium forms of the enzyme reached a maximum after 4 days of treatment. In epididymis only the epithelial form of 5α-reductase underwent a major change in specific activity, the latter peaking after 8–12 days of treatment. Furthermore, while the total activity of 5α-reductase in the prostatic tissue fractions could be induced by as much as 4-fold the normal control values, the epididymal enzyme could not be induced above the normal level either in the stroma or the epithelium. This may explain the relative resistance of epididymis to abnormal growth stimulation under the influence of hormones.

scholarly journals Characterization of bacteriocin and chitinase producing bacterial isolates with broad-spectrum antimicrobial activities

2021 ◽  
Vol 3 (8) ◽  
Author(s):  
Muhammad Yasir ◽  
Basit Zeshan ◽  
Nur Hardy A. Daud ◽  
Izzah Shahid ◽  
Hafza Khalid
Keyword(s):  
Antimicrobial Activity ◽  
Inhibitory Activity ◽  
Antifungal Drugs ◽  
Proteinase K ◽  
Diffusion Method ◽  
List Type ◽  
Bacterial Isolates ◽  
E Coli ◽  
Inhibitory Potential

Abstract There is a need for more efficient and eco-friendly approaches to overcome increasing microbial infections. Bacteriocins and chitinases from Bacillus spp. can be powerful alternatives to conventional antibiotics and antifungal drugs, respectively. The purpose of this study was to assess the inhibitory potential of bacteriocins and chitinase enzymes against multiple resistant bacterial and fungal pathogens. Bacterial isolates were selected by growth on minimal salts medium and after that were morphologically and biochemically characterized. The physiochemical characterization of bacteriocins was carried out. The inhibitory potential of bacteriocins towards six pathogenic bacteria was determined by the well diffusion assay while chitinase activity towards three fungal strains was determined by the dual plate culture assay. Two bacterial strains (WW2P1 and WRE4P2), out of nine showed inhibition of K. pneumonia, P. aeruginosa, E. coli and MRSA while WW4P2 was positive against S. typhimurium and E. coli and WRE10P2 against P. aeruginosa, S. pneumoniae. Two bacterial isolates (WW3P1 and WRE10P2) were chosen for further study on the basis of their antifungal activities. Of these, WW3P1 isolate was more effective against A. fumigatus as well as A. niger. The proteinaceous nature of the bacteriocins was confirmed by treatment of the crude extract with proteinase K. It was found that the inhibitory activity of strain WW3P1 against E. coli was highest at 20 °C, and against S. pneumoniae it was at 20 °C and pH 10 after treatment with EDTA. Inhibition by strain the WRE10P2 against P. aeruginosa was highest at 20 °C and pH 14. It was found that EDTA increased the inhibitory activity of strain WW2P1 against P. aeruginosa, K. pneumoniae and E. coli by 2 ± 0.235, 3.5 ± 0.288, 2.5 ± 1.040 times, respectively, of strain WRE4P2 against P. aeruginosa and E. coli by 2.5 ± 0.763, 2.7 ± 0.5 times, respectively, and of strain WRE10P2 against S. pneumoniae by 3 ± 0.6236 times. The isolates have promising inhibitory activity, which should be further analyzed for the commercial production of antimicrobials. Article highlights The current study aimed to isolate the microbiome from wheat plant (Triticum aestivum L.), to screen for bacteriocin production and to assess its antimicrobial activity against human pathogens. Forty-one phenotypically different bacterial colonies were subjected to bacteriocin purification from which 25 colonies showed positive reactions. These 25 bacterial isolates were screened against six different human bacterial pathogens using the well diffusion method to check the antimicrobial activity. Out of nine bacterial isolates, WW3P1 and WRE10P2 were able to degrade the chitin and utilize it as their sole energy source. Strain WRE4P2 exhibited partial inactivation in its activity against MRSA after treatment with proteinase K.

Tyrosinase Inhibitory Activity of Flavonoids from Artocarpus Lowii King

2014 ◽  
Vol 71 (1) ◽  
Author(s):  
Shajarahtunnur Jamil ◽  
Siti Awanis Abdullah ◽  
Siti Mariam Abdul Lathiff ◽  
Hasnah Mohd Sirat
Keyword(s):  
Inhibitory Activity ◽  
Kojic Acid ◽  
Mushroom Tyrosinase ◽  
Tyrosinase Inhibitory Activity ◽  
Crude Extracts ◽  
Ic50 Value ◽  
Microplate Reader

Tyrosinase inhibitory activity was studied on the crude extracts and flavonoids successfully isolated from the leaves and heartwoods of Artocarpus lowii King. The flavonoids were fully characterized spectroscopically as isobavachalcone (1), 4-hydroxyonchocarpin (2), 2',4'-dihydroxy-4-methoxy-3'-prenyldihydrochalcone (3), 2',4'-dihydroxy-3,4-(2",2"-dimethylchromeno)-3'-prenyldihydrochalcone (4), artocarpin (5), cycloheterophyllin (6) and 4',5-dihydroxy-6,7-(2,2-dimethylpyrano)-2'-methoxy-8-γ,γ-dimethyl allylflavone (7). Tyrosinase inhibitory activity of the samples was determined against mushroom tyrosinase using ELISA microplate reader. Cycloheterophyllin (6) exhibited an excellent inhibitory activity against mushroom tyrosinase comparable to the standard kojic acid with the IC50 value of 52.5 µg/mL (88.3%).

Quantitative Evaluation of Allelopathic Potentials in Soils: Total Activity Approach

Weed Science ◽  
2010 ◽  
Vol 58 (3) ◽  
pp. 258-264 ◽  
Author(s):  
Syuntaro Hiradate ◽  
Kenji Ohse ◽  
Akihiro Furubayashi ◽  
Yoshiharu Fujii
Keyword(s):  
Cinnamic Acid ◽  
Specific Activity ◽  
Quantitative Estimation ◽  
Alluvial Soil ◽  
Total Activity ◽  
Mucuna Pruriens ◽  
Maximum Effect ◽  
Published Data ◽  
Plant Materials ◽  
Allelopathic Potential

The allelopathic potential of a plant has been evaluated on the basis of two indicators: specific activity, which is the specific concentration of the allelochemical to exert a half-maximum effect on a receiver plant (EC50), and total activity in a plant, which is the ratio of the concentration of an allelochemical in the producing plant to its EC50. In the present study, a new indicator, total activity in a soil, which takes into account the effects of a soil on the allelopathy activity, is proposed because allelopathic activity is affected by the presence of soils. The total activity in a soil was calculated by multiplying the “total activity in a plant” with a “soil factor.” In this calculation, we assumed simplified cases for comparison, such that the allelopathic plant materials are evenly incorporated in the soils and the allelochemicals are released from the plant materials to the soils at a constant rate. We conducted bioassay experiments in the presence and absence of soils and cited some published data to calculate the specific activities and total activities in a plant and in a soil. The results indicated that the allelopathies of buckwheat caused by (+)-catechin, Leucaena leucocephala by L-mimosine, Xanthium occidentale by trans-cinnamic acid, and Brassica parachinensis by cis-cinnamic acid were not significant in a volcanic ash soil, an alluvial soil, and a calcareous soil, but the allelopathy of sweet vernalgrass caused by coumarin and Spiraea thunbergii by cis-cinnamoyl glucosides was highly effective in those soils. The allelopathies of Juglans species caused by juglone plus juglone precursors and Mucuna pruriens by L-DOPA would depend highly on the soil types. Although some limitations exist for this approach, the total activity approach would allow for a better quantitative estimation of the allelopathic potential of plant materials in soils.

scholarly journals Covalent Immobilization of Thiol Proteinases on Chitosan

2020 ◽  
Vol 2 (1) ◽  
pp. 7
Author(s):  
Svetlana Olshannikova ◽  
Victoria Koroleva ◽  
Marina Holyavka ◽  
Alexander Pashkov ◽  
Valeriy Artyukhov
Keyword(s):  
Specific Activity ◽  
Crosslinking Agent ◽  
Total Activity ◽  
Covalent Immobilization ◽  
Tropical Plants ◽  
Chitosan Matrix ◽  
Plant Enzymes ◽  
Thiol Proteases ◽  
Thiol Proteinases ◽  
Wide Substrate Specificity

Plant enzymes such as ficin (EC 3.4.22.3), papain (EC 3.4.22.2) and bromelain (EC 3.4.22.4) are obtained from tropical plants. These biocatalysts belong to thiol proteases, in the active center of which cysteine is contained. Ficin, papain and bromelain have a wide substrate specificity, which provides a demand for their use in various industries. Enzymes in the free state are less commonly used; immobilized biocatalysts are the preferred form. The aim of this work was to determine the optimal concentration of a crosslinking agent in the covalent immobilization of ficin, papain and bromelain on a chitosan matrix. Ficin, papain and bromelain (Sigma) were chosen as objects of study. An acid-soluble chitosan (350 kDa, Bioprogress CJSC) was used as an immobilization carrier. The concentration range of glutaraldehyde (crosslinking agent) ranged from 1 to 25%. Suitable concentrations of glutaraldehyde for covalent immobilization were identified by the optimal ratio of protein content (mg per g of carrier), total activity (in units per ml of solution) and specific activity (in units per mg of protein). It was shown that for covalent immobilization of ficin and bromelain on a chitosan matrix, it is most promising to use 10% glutaraldehyde. For immobilization of papain on chitosan by covalent means, the concentration of glutaraldehyde equal to 20% is optimal.

Changes in the peroxidase activity of subcellular fractions from aging Phaseolus hypocotyls

1975 ◽  
Vol 53 (9) ◽  
pp. 852-860 ◽  
Author(s):  
B. Truelove ◽  
R. Rodriguez-Kabana ◽  
Larry R. Jones
Keyword(s):  
Phaseolus Vulgaris ◽  
Peroxidase Activity ◽  
Specific Activity ◽  
Total Activity ◽  
Chronological Age ◽  
Phaseolus Vulgaris L ◽  
Soluble Peroxidase ◽  
Tissue Homogenates ◽  
Hypocotyl Tissue ◽  
Nitrogen Contents

Changes in nitrogen contents and peroxidase activities of fractions isolated from hypocotyl tissue of Black Valentine bean (Phaseolus vulgaris L.) of increasing age were studied. As beans aged in darkness, a decreasing percentage of their nitrogen content was recovered in the isolated particulate fractions. Peroxidase activity of particulate fractions from dark-grown beans accounted for 49% of the total activity of both 3-day-old seedlings and 16-day-old senescing plants. Peroxidase specific activity of dark-grown tissue homogenates did not increase with plant age; however, after a certain period of growth, further aging resulted in increased peroxidase specific activity associated with the particulate fractions. Between day 3 and day 8 the patterns of peroxidase activity of the different fractions varied, but over the period day 9 to day 16, the patterns of all fractions were correlated. The nitrogen contents and peroxidase activities of fractions isolated from beans transferred from dark to light were different from those of fractions from beans of similar chronological age kept in darkness. Transfer of plants to light resulted in increased soluble peroxidase activity and prevention of the steep increase in particulate fraction activity recorded for dark-grown plants.

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