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1.
Food Chem ; 227: 102-110, 2017 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-28274409

RESUMO

The hunt for anti-browning agents in the food and agricultural industries aims to minimize nutritional loss and prolong post harvest storage. In the present study, the effect of cyanidin-3-sophoroside (CS) from Garcinia mangostana rind, on polyphenol oxidase (PPO) activity was investigated. The non-competitive inhibition mode of CS was determined by Lineweaver Burk plot. CS forms a ground-state complex by quenching the intrinsic fluorescence of PPO. The static quenching was temperature-dependent with an activation energy of 4.654±0.1091kJmol-1 to withstand the disruption of amino acid residues of the enzyme binding site. The enzyme conformational change was validated by 3D fluorescence and CD spectrum. Docking (binding energy -8.124kcal/mol) and simulation studies confirmed the binding pattern and stability. CS decreased PPO activity and browning index of fresh cut apples and prolonged the shelf life. Thus, CS appears to be a promising anti-browning agent to control enzymatic browning.


Assuntos
Antocianinas/metabolismo , Catecol Oxidase/metabolismo , Malus/metabolismo , Proteínas de Plantas/metabolismo , Antocianinas/química , Catecol Oxidase/química , Cor , Malus/química , Malus/enzimologia , Simulação de Acoplamento Molecular , Oxirredução , Proteínas de Plantas/química
2.
Artigo em Inglês | MEDLINE | ID: mdl-26913965

RESUMO

Catechin, a yellow colored molecule obtained from the wood of Acacia catechu was analyzed for its interaction with synthetic DNA duplexes using spectroscopic analysis. UV-Visible spectroscopic analysis revealed the non-intercalative binding mode. Fourier Transform Infrared spectroscopy (FTIR) analysis expose chemical shift indicated by various vibrational stretches and an increase in the intensity of base stacking was observed by Circular Dichroism (CD), respectively. This inference was further confirmed through nuclear staining technique and also in electrophoretic technique; the dye quenches the fluorescent intensity of ethidium bromide. The result of fluorescence spectroscopy was in concordance with the electrophoretic technique. In addition, the spectroscopic results were in accordance with the molecular docking studies of specific catechin compound from the catechu dye with CT-DNA. This kind of site specificity is a gain in the medicinal field as the drug can be DNA targeted for cancer therapeutics. The present work reveals that catechu dye has a noteworthy application in the field of medical bioscience.


Assuntos
Catequina/química , DNA/química , Interações Hidrofóbicas e Hidrofílicas , Simulação de Acoplamento Molecular , Análise Espectral
3.
J Biosci Bioeng ; 121(1): 13-20, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26187443

RESUMO

In this present study, the inhibitory mechanism of three selected apocarotenoids (bixin, norbixin and crocin) on the diphenolase activity of tyrosinase has been investigated. The preliminary screening results indicated that apocarotenoids inhibited tyrosinase activity in a dose-dependent manner. Kinetic analysis revealed that apocarotenoids reversibly inhibited tyrosinase activity. Analysis of fluorescence spectra showed that apocarotenoids quenched the intrinsic fluorescence intensity of the tyrosinase. Further, molecular docking results implied that apocarotenoids were allosterically bound to tyrosinase through hydrophobic interactions. The results of the in vitro studies suggested that higher concentrations of bixin and norbixin inhibited tyrosinase activity in B16F0 melanoma cells. Our results suggested that apocarotenoids could form the basis for the design of novel tyrosinase inhibitors.


Assuntos
Carotenoides/farmacologia , Monofenol Mono-Oxigenase/antagonistas & inibidores , Sítio Alostérico , Animais , Linhagem Celular Tumoral , Relação Dose-Resposta a Droga , Interações Hidrofóbicas e Hidrofílicas , Cinética , Melaninas/biossíntese , Melanoma/enzimologia , Camundongos , Simulação de Acoplamento Molecular , Monofenol Mono-Oxigenase/metabolismo , Ligação Proteica , Espectrometria de Fluorescência
4.
Environ Toxicol ; 31(9): 1059-67, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25926096

RESUMO

Natural toxins from plant sources with wide ranges of biological activities reflect the upswing of drug design in the pharmaceutical industry. Rubia cordifolia L. is one of the most important red dye yielding plants. Most of the former researches have focused on the bioactive compounds from the roots of R. cordifolia, while no attention was paid towards the fruits. For the first time, here we report the presence of dibutyl phthalate in the fruits of R. cordifolia. Structural characterization was carried out using Ultraviolet-Visible spectrophotometer (UV-Vis), Fourier transform infrared (FTIR), gas chromatography-mass spectrophotometer (GC-MS), Nuclear magnetic resonance (NMR). Acute toxicity of the crude ethanolic extracts of the R. cordifolia fruits was examined in Swiss albino mice. No mortality was observed in all treated mice with 100, 500, 1000 mg/kg body weight of crude extract of R. cordifolia fruit and it indicates that the LD50 value is higher than 1000 mg/kg body weight. This study exhibited a significant change in the body weight. Alanine transaminase (ALT), total protein, triglycerides, glucose, and also the histopathological analysis of liver for all treated mice showed difference from the control group. The dibutyl phthalate was further evaluated for the toxicity study through in silico analysis. Together, the results highlighted that the toxic potential of R. cordifolia fruits extracts and also the toxicity profile of the fruit should be essential for the future studies dealing with the long term effect in animals. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 1059-1067, 2016.


Assuntos
Dibutilftalato/toxicidade , Fígado/efeitos dos fármacos , Extratos Vegetais/química , Rubia/química , Alanina Transaminase/metabolismo , Animais , Peso Corporal/efeitos dos fármacos , Dibutilftalato/química , Dibutilftalato/isolamento & purificação , Feminino , Frutas/química , Frutas/metabolismo , Cromatografia Gasosa-Espectrometria de Massas , Fígado/metabolismo , Fígado/patologia , Espectroscopia de Ressonância Magnética , Camundongos , Raízes de Plantas/química , Raízes de Plantas/metabolismo , Rubia/metabolismo , Espectroscopia de Infravermelho com Transformada de Fourier , Testes de Toxicidade Aguda , Triglicerídeos/metabolismo
5.
Artigo em Inglês | MEDLINE | ID: mdl-25754392

RESUMO

The interaction of food colorant norbixin with calf thymus DNA (CTDNA) was investigated through UV-Visible spectroscopy, Fourier Transform Infrared (FTIR), Circular Dichroism (CD), Nuclear Magnetic Resonance (NMR), DNA melting studies, electrophoretic analysis, histological staining technique and molecular docking studies. The results indicated that norbixin interacted with CTDNA by partial intercalation mode. The binding constant (K) of norbixin with CTDNA was calculated to be 5.08×10(5) Mol(-1) L. FTIR and CD studies were coupled with (1)H NMR spectra revealed that norbixin intercalates partially and binds to the groove's, phosphate group, deoxyribose sugar of DNA and also induces conformational transition of B-form to A-form DNA. Agarose gel electrophoretic and histological staining technique results further prove that, norbixin specifically binds to the DNA in the cell. Moreover, molecular docking studies on the specific binding of norbixin with CTDNA have exhibited lowest conformation energy score of -3.2. Therefore, this food colorant has the ability to interact with DNA and it could emerge as a promising class of natural DNA targeted therapeutic.


Assuntos
Carotenoides/metabolismo , Simulação por Computador , DNA/metabolismo , Animais , Carotenoides/química , Bovinos , Dicroísmo Circular , DNA/química , Eletroforese em Gel de Ágar , Conformação Molecular , Simulação de Acoplamento Molecular , Desnaturação de Ácido Nucleico , Cebolas/citologia , Espectroscopia de Prótons por Ressonância Magnética , Espectrofotometria Ultravioleta , Espectroscopia de Infravermelho com Transformada de Fourier , Coloração e Rotulagem
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