Mohammad Sukmanadi
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Detection of Mycotoxigenic Fungi on Food from Markets with the Polymerase Chain Reaction Method for Halal and Thoyiban Food Mohammad Sukmanadi; Retno Sri Wahjuni; Kadek Rachmawati
Indian Journal of Forensic Medicine & Toxicology Vol. 15 No. 2 (2021): Indian Journal of Forensic Medicine & Toxicology
Publisher : Institute of Medico-legal Publications Pvt Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37506/ijfmt.v15i2.14813

Abstract

Secondary metabolites of filamentous mold are mycotoxins, which in some situations can develop on foodsderived from plants or from animals. Fusarium, Aspergillus, and Penicillium are the most common types ofmold that produce mycotoxins and also often contaminate human food and animal feed. Aflatoxins includingaflatoxin B1, B2, G1 and G2 are produced by A. flavus and A. parasiticus. M1 and M2 aflatoxins arefound in dairy products. In this study, we used PCR to detect and identify mycotoxigenic fungi material infoods from traditional markets and supermarkets in Surabaya, Indonesia. Samples of chicken meat from atraditional market and from a supermarket (10 pieces each) were placed in a conical tube and crushed in PBS.The crushed samples were centrifuged and the supernatants were cultured on potato dextrose agar (PDA)media and observed using a reverse microscope. DNA was isolated from cultured samples and subjectedto PCR with primers specific for genes encoding aflatoxins. Interestingly, we revealed that the PolymeraseChain Reaction (PCR) analysis showed A. flavus and A. ochraceus were present on chicken meat sold attraditional markets and supermarkets. In sum, enhanced precautions may be needed to ensure that foods soldin traditional markets and supermarkets are free from molds that have the potential to produce mycotoxins.Further studies are needed to detect and identify the prevalence of mycotoxins in the food supply.
Analysis of Capsicum annuum L. Methanolic Extract and Its Potential as a Hepatoprotector Mustofa Helmi Effendi; Mohammad Sukmanadi
Indian Journal of Forensic Medicine & Toxicology Vol. 15 No. 3 (2021): Indian Journal of Forensic Medicine & Toxicology
Publisher : Institute of Medico-legal Publications Pvt Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37506/ijfmt.v15i3.15869

Abstract

ThinLayerChromatography(TLC) method performed to purify capsaicin compound in C. annum L. and test the bioactive component of Capsicum Annum L on MAPK1 target proteins using the Immunohistochemistry (IHC) method to determine the reactions between receptor-ligand (antigen-antibody) complexes formed and become a reference in vivo tests. Natural ingredients need to be extracted to get some or all of the active ingredients used to synthesize the right dosage, easily stored, and maintain for a long time. The active ingredient of capsaicin is efficacious as a stimulant of gastric acid secretion and prevents infections in the digestive system.The immunohistochemical examination is intended to determine the expression of MAPK1 (ERK) on cells of mice hepatocytes (Mus musculus). MAPK 1 (ERK) expression score data were obtained using the modified Remmele method is the result of multiplying the percentage score of immunoreactive cells with the color intensity score on immunoreactive cells. The abnormal target protein signaling pathway contributes to cell proliferation, differentiation, survival, and uncontrolled cell apoptosis.Analysis of amino acid residues, Capsaicin to MAPK1haverelativelysimilarresiduessothatitcanbeconcludedthat the binding sites of the two compounds are close to similarities and affect receptors at relatively similar sites, namely oncogenicreceptors/ proteins. Concluded that the ethanol extract of Capsicum. annum L. had a greater in the powder form , TLC method showed the capsaicin standard was 1020 µg/ml, that capsaicin in chilies (Capsicum Annum L.) can synergistically inhibit cell through reactions in the anti-apoptotic MAPK 1 potentiates the antiproliferative action that can promote hepatoprotector, a finding that demands further clinicaltesting.