Melanin Synthesized by the Endophytic Aureobasidium Pullulans AKW: A Multifaceted Biomolecule with Antioxidant, Wound Healing, and Selective Anti-Cancer Activity

Author:

Elattar Khaled M.1,Ghoniem Abeer A.2,Al-Askar Abdulaziz A.3,El-Gazzar Usama Bhgat4,El-Hersh Mohammed S.5,Elsherbiny Elsherbiny A.6,Eldadamony Noha M.7,Saber WesamEldin I.A.5

Affiliation:

1. Unit of Genetic Engineering and Biotechnology, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura, 35516, Egypt

2. Microbial Activity Unit, Department of Microbiology, Soils, Water and Environment Research Institute, Agricultural Research Center, Giza12619, Egypt

3. Botany and Microbiology Department, Faculty of Science, King Saud University, Riyadh11451, Saudi Arabia

4. Department of Medical Biochemistry, Damietta Faculty of Medicine, Al-Azhar University, Egypt

5. Microbial Activity Unit, Department of Microbiology, Soils, Water and Environment Research Institute, Agricultural Research Center, Giza12619, Egypt

6. Department of Biology, Rheinland-Pfälzische Technische Universität Kaiserslautern (RPTU), 67663Kaiserslautern, Germany

7. Seed Pathology Department, Plant Pathology Research Institute, Agricultural Research Center, Giza12619, Egypt

Abstract

Introduction: This study explores the potential of the endophytic fungus Aureobasidium pullulans AKW for melanin production and its anticancer activity. Method: We report a significant achievement: A. pullulans AKW synthesized 4.89 g/l of melanin in a simple fermentation medium devoid of tyrosine, a precursor typically required for melanin biosynthesis. This suggests a potentially novel pathway for melanin production compared to previous studies relying on complex media and tyrosine. Furthermore, the isolated and characterized melanin exhibited promising selectivity as an anti-cancer agent. It triggered apoptosis in A431 cancer cells, demonstrating some selectivity compared to normal cells. This selectivity was confirmed by IC50 values and further supported by gene expression changes in A431 cells. Melanin treatment downregulated the anti-apoptotic Bcl2 gene while upregulating pro-apoptotic Bax and p53 genes, indicating its ability to induce programmed cell death in cancer cells. Result: Our results demonstrate that A. pullulans AKW-derived melanin exhibits cytotoxic effects against A431, HEPG2, and MCF7 cell lines. Interestingly, the present fungal strain synthesized melanin in a simple medium without requiring precursors. Conclusion: The selective activity of the current melanin towards cancer cells, its ability to induce apoptosis, and its relatively low toxicity towards normal cells warrant further investigation for its development as a novel therapeutic option.

Publisher

Bentham Science Publishers Ltd.

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