Bioactivity and Chemical Profiling of Medicinal Fungi Inonotus cuticularis and Inocutis levis (Hymenochaetaceae) using Chromatography and Mass Spectrometry

Publish Year: 1403
نوع سند: مقاله ژورنالی
زبان: English
View: 57

This Paper With 13 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_JJMPB-13-1_016

تاریخ نمایه سازی: 8 بهمن 1402

Abstract:

Polypore fungi are among the most preventable mushroom-forming fungi with known therapeutic potential, though only a few species have been securitized for their metabolites. This study examines the biological activity and bioactive compounds of Inocutis levis and Inonotus cuticularis collected in Iran. We examined the antimicrobial, antioxidant, and cytotoxic properties of n-hexane, acetone, and ethyl acetate extracts. Chemical profiles were assessed by chromatography and mass spectroscopy techniques. The acetonic extracts exhibited the highest antibacterial effect against all tested microbial strains. The IC۵۰ values for DPPH and ABTS assays ranged from ۱۴۴.۹۸ – ۴۶۹.۰۲ μg/mL and ۱۲۸.۰۶ – ۳۳۱.۵۲ μg/mL, respectively. The MTT assays for both fungi indicated low toxicity on normal HDF cells with IC۵۰ values ranging from ۱۴۴۷ to ۱۹۰۸ μg/mL. HPLC-DAD analysis showed a high level of gallic acid among other detected phenolic compounds. LC-ESI-MS/MS analysis displayed the presence of various sesquiterpenoids, furans, and styrylpyrone-class compounds. Inotilone, inonotin H and C, phellinulin B and M, cinnamic acid, p-coumaric acid, caffeic acid, phelligridin A and D, hispidin, and gallic acid were found in both species. Daedalin A is reported for the first time from the fungal family Hymenochaetaceae. In addition, several volatile compounds, including alkene hydrocarbons and some fatty acids, such as linoleic acid, were detected in GC-MS analyses. We suggest that I. levis and I. cuticularis have dual antibacterial and antioxidant properties and diverse metabolites, potentially opening new windows in future natural product-based medicine.

Authors

Samaneh Chaharmiri-Dokhaharani

Department of Biotechnology, Iranian Research Organization for Science and Technology (IROST), P. O. Box ۳۳۵۳-۵۱۱۱, Tehran, Iran

Masoomeh Ghobad-Nejhad

Department of Biotechnology, Iranian Research Organization for Science and Technology (IROST), P. O. Box ۳۳۵۳-۵۱۱۱, Tehran, Iran

Hamid Moghimi

Department of Microbial Biotechnology, School of Biology, College of Science, University of Tehran, Tehran, Iran

Hooman Norouzi

Department of Horticultural Sciences, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Iran

Mohaddeseh Moghaddam

Department of Biotechnology, Iranian Research Organization for Science and Technology (IROST), P. O. Box ۳۳۵۳-۵۱۱۱, Tehran, Iran

مراجع و منابع این Paper:

لیست زیر مراجع و منابع استفاده شده در این Paper را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود Paper لینک شده اند :
  • Grienke U., Zöll M., Peintner U., Rollinger J.M. European medicinal ...
  • Thu ZM, Myo KK, Aung HT, Clericuzio M, Armijos C, ...
  • Venturella G, Ferraro V, Cirlincione F, Gargano ML. Medicinal mushrooms: ...
  • Adongbede EM, Jaiswal YS, Davis SS, Randolph PD, Huo LN, ...
  • Ghobad-Nejhad M, Kotiranta H. The genus Inonotus sensu lato in ...
  • Ravera S, Vizzini A, Puglisi M, Adamčík S, Aleffi M, ...
  • Ying, C.-c., Icons of medicinal fungi from China. ۱۹۸۷: Science ...
  • Zhao J. The resources and application of medicinal fungi from ...
  • Guo L, Ma JY, Ma YZ, Zhang TL, Mao SL, ...
  • Dai YC, Yang ZL, Cui BK, Yu CJ, Zhou LW. ...
  • Ehsanifard Z, Mir-Mohammadrezaei F, Safarzadeh A, Ghobad-Nejhad M. Aqueous extract ...
  • Ehsanifard Z, Mir Mohammadrezaei F, Ghobad-Nejhad M, Safarzade AR. The ...
  • Wu F, Zhou LW, Yang ZL, Bau T, Li TH, ...
  • Chaharmiri Dokhaharani S., Ghobad-Nejhad M., Moghimi H., Farazmand A., Rahmani ...
  • Cui Y., Kim D-S., Park K-C. Antioxidant effect of Inonotus ...
  • Wayne P. CLSI. Performance Standards for Antimicrobial Susceptibility Testing. CLSI ...
  • Procop G.W. M۶۰, Performance standards for antifungal susceptibility testing of ...
  • Béni Z, Dékány M, Kovács B, Csupor-Löffler B, Zomborszki ZP, ...
  • Bach F., Zielinski A.A., Helm C.V., Maciel G.M., Pedro A.C., ...
  • Waterhouse, A.L., Determination of total phenolics. Curr. protoc. food anal. ...
  • DuBois M., Gilles K.A., Hamilton J.K., Rebers P.T., Smith F. ...
  • Kolundžić M., Grozdanić N.Đ., Dodevska M., Milenković M., Sisto F., ...
  • Dokhaharani S.C., Ghobad-Nejhad M., Moghimi H., Farazmand A., Rahmani H. ...
  • Asgharpour F., Moghadamnia A.A., Alizadeh Y, Kazemi S. Chemical Composition ...
  • Liu K., Xiao X., Wang J., Chen C.Y., Hu H. ...
  • Hur J.M., Yang CH., Han SH., Lee SH., You Y.O., ...
  • Breijyeh Z., Jubeh B., Karaman R. Resistance of gram-negative bacteria ...
  • Negi P. Jayaprakasha G. Antioxidant and antibacterial activities of Punica ...
  • Tamrakar S., Nishida M., Amen Y., Tran H.B., Suhara H., ...
  • Angelini P., Girometta C., Tirillini B., Moretti S., Covino S., ...
  • Stajić M, Vukojević J, Ćilerdžić J. Mushrooms as potential natural ...
  • Song Y., Hui J., Kou W., Xin R., Jia F., ...
  • Rajamanickam K., J. Yang, and M.K. Sakharkar, Gallic acid potentiates ...
  • Darkal A.K., Zuraik M.M., Ney Y., Nasim M.J., Jacob C. ...
  • Sova, M., Antioxidant and antimicrobial activities of cinnamic acid derivatives. ...
  • Lee, I.-K. and B.-S. Yun, Styrylpyrone-class compounds from medicinal fungi ...
  • Liu C., Zhao C., Pan H.H., Kang J., Yu X.T., ...
  • Handa, N., Yamada T., Tanaka R. An unusual lanostane-type triterpenoid, ...
  • Morimura K., Yamazaki C., Hattori Y., Makabe H., Kamo T., ...
  • Morimura K., Hiramatsu K., Yamazaki C., Hattori Y., Makabe H., ...
  • Liu Y., Kubo M., Fukuyama Y. Nerve growth factor-potentiating benzofuran ...
  • Han J.J., Bao L., He L.W., Zhang X.Q., Yang X.L., ...
  • Lee I.K., Han M.S., Lee M.S., Kim Y.S., Yun B.S. ...
  • Jeon Y.E., Lee Y.S., Lim S.S., Kim S.J., Jung SH., ...
  • Zhang B, Zhou J, Li Q, Gan B, Peng W, ...
  • Wang Z.X., Feng X.L., Liu C., Gao J.M., Qi J. ...
  • Bergmann P., Takenberg M., Frank C., Zschätzsch M., Werner A., ...
  • Nakajima Y., Nishida H., Nakamura Y., Konishi T. Prevention of ...
  • Glamočlija J., Ćirić A., Nikolić M., Fernandes Â., Barros L, ...
  • Pubchem, CID ۲۱۳۱۵۶۹۸. ۳-(Hexyloxy)-۴-hydroxybenzaldehyde. https://pubchem.ncbi.nlm.nih.gov/compound/۲۱۳۱۵۶۹۸ ...
  • Nyigo V., Baraza L.D., Nkunya M.H., Mdachi S.J., Joseph C.C., ...
  • Lee I.K., Seok S.J., Kim W.K., Yun BS.Hispidin Derivatives from ...
  • Isaka M., Yangchum A., Supothina S., Boonpratuang T., Choeyklin R., ...
  • Chao W., Deng J.S., Li P.Y., Kuo Y.H., Huang G.J. ...
  • Kojima K., Ohno T., Inoue M., Mizukami H., Nagatsu A. ...
  • Huang S.C., Wang P.W., Kuo P.C., Hung H.Y., Pan T.L. ...
  • Ohyoshi T., Mitsugi K., Higuma T., Ichimura F., Yoshida M, ...
  • Serck-Hanssen K., Wikström C. Novel ۷-phenylheptan-۳-ones from the fungus Phellinus ...
  • Nelson, G.J., D.P. Matthees, and D.E. Lewis, ۱-Phenylheptane-۱, ۵-dione from ...
  • Reis F.S., Barreira J.C., Calhelha R.C., van Griensven L.J., Ćirić ...
  • Olennikov D.N., Sof'ya V.A., Tat'yana A.P., Borovski GB. Fatty acid ...
  • Deng K., Zhang Y., Ren Z., Xie L., Peng W., ...
  • Vazirian M., Faramarzi M.A., Ebrahimi S.E., Esfahani H.R., Samadi N., ...
  • Göring, H. Vitamin D in nature: a product of synthesis ...
  • Rajakumar K., Greenspan S.L., Thomas S.B., Holick M.F. SOLAR ultraviolet ...
  • Yazawa Y., Yokota M., Sugiyama K. Antitumor promoting effect of ...
  • Sun Y., Yin T., Chen X.H., Zhang G., Curtis R.B., ...
  • Kusumah D., Wakui M., Murakami M., Xie X., Yukihito K., ...
  • Wu S., Krings U., Zorn H., Berger R.G. Volatile compounds ...
  • Aisala H., Sola J., Hopia A., Linderborg K.M., Sandell M.Odor-contributing ...
  • نمایش کامل مراجع