Cited by 57Microbial Metabolism and ApplicationsMicrobial Natural Products and Biosynthesismelanin and skin pigmentation

Melanin in fungi: Advances in structure, biosynthesis, regulation, and metabolic engineering

Open access
Qin, Yanping, Xia, Yuxian·2024·Microbial Cell Factories

Abstract

Fungi can synthesize a diverse range of melanins with appropriate physicochemical and biological characteristics for numerous applications in health, environmental protection, energy, and industry. Gaining deeper insights into the chemical structures, biosynthetic pathways, and regulatory mechanisms of fungal melanin would establish a basis for metabolic engineering approaches, aimed at enhancing production efficiency and creating custom-designed melanin with desirable material properties. Due to growing interest in their beneficial effects and applications, research on the structure, biosynthesis, and regulation of fungal melanin has significantly advanced. This review highlighted recent progress in fungal melanin production and applications, concentrating on structure, biosynthesis, and regulatory networks, and suggested how an improved understanding of melanin biosynthesis could enable efficient production for future applications.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1186/s12934-024-02614-8

Cites

3 of 3 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The entire DHN melanin pathway involves five key catalytic enzymes.

    “This entire pathway involves five key catalytic enzymes [29] (Figure 3A).”

    From Fungal Melanin in Plant Pathogens: Complex Biosynthesis Pathways and Diverse Biological Functions (2025) · cites this paper as [29]

    The “Biosynthesis of fungal melanin > DHN-melanin” section describes several catalytic steps and names PKS, T4HN reductase, and laccase. It does not state that the entire pathway has exactly five key catalytic enzymes; it also notes that the pathway differs among fungi. The enzyme count is therefore unsupported. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 204

  1. [1]Riley PA. Melanin. Int J Biochem Cell Biol. 1997;29:1235–9. 9451820 · DOI
  2. [3]Kalra R, Conlan XA, Goel M. Fungi as a potential source of pigments: harnessing filamentous fungi. Front Chem. 2020. 10.3389/fchem.2020.00369. 32457874 PMC7227384 · DOI
  3. [4]Eisenman HC, Greer EM, McGrail CW. The role of melanins in melanotic fungi for pathogenesis and environmental survival. Appl Microbiol Biot. 2020;104:4247–57. 32206837 · DOI
  4. [5]Derby CD. Cephalopod ink: production, chemistry, functions and applications. Mar Drugs. 2014;12:2700–30. 24824020 PMC4052311 · DOI
  5. [6]Nie LF, Huang G, Bozorov K, Zhao J, Niu C, Sagdullaev SS, et al. Diversity-oriented synthesis of amide derivatives of tricyclic thieno[2,3-d]pyrimidin-4(3H)-ones and evaluation of their influence on melanin synthesis in murine B16 cells. Heterocycl Commun. 2018;24:43–50. · DOI
  6. [7]Revskaya E, Chu P, Howell RC, Schweitzer AD, Bryan RA, Harris M, et al. Compton scattering by internal shields based on melanin-containing mushrooms provides protection of gastrointestinal tract from ionizing radiation. Cancer Biother Radiol. 2012;27:570–6. PMC3484786 23113595
  7. [8]Durán N, Teixeira MFS, De Conti R, Esposito E. Ecological-friendly pigments from fungi. Crit Rev Food Sci. 2002;42:53–66. 11837241 · DOI
  8. [9]Dufossé L, Fouillaud M, Caro Y, Mapari SA, Sutthiwong N. Filamentous fungi are large-scale producers of pigments and colorants for the food industry. Curr Opin Biotech. 2014;26:56–61. 24679259 · DOI
  9. [10]Cordero RJB, Casadevall A. Functions of fungal melanin beyond virulence. Fungal Biol Rev. 2017;31:99–112. 31649746 PMC6812541 · DOI
  10. [11]El-Naggar NE-A, Saber WIA. Natural melanin: current trends, and future approaches, with especial reference to microbial source. Polymers. 2022;14:1339. 35406213 PMC9002885 · DOI
  11. [12]Gessler NN, Egorova AS, Belozerskaya TA. Melanin pigments of fungi under extreme environmental conditions (review). Appl Biochem Microbiol. 2014;50:105–13. 25272728 · DOI
  12. [13]Mattoon E, Cordero R, Casadevall A. Fungal melanins and applications in healthcare, bioremediation and industry. JoF. 2021. 10.3390/jof7060488. 34207260 PMC8235761 · DOI · Paper page
  13. [14]Wang Y, Aisen P, Casadevall A. Melanin, melanin “ghosts”, and melanin composition in Cryptococcus neoformans. Infect Immun. 1996;64:2420–4. 8698461 PMC174092 · DOI · Paper page
  14. [15]Prados-Rosales R, Toriola S, Nakouzi A, Chatterjee S, Stark R, Gerfen G, et al. Structural characterization of melanin pigments from commercial preparations of the edible mushroom Auricularia auricula. J Agric Food Chem. 2015;63:7326–32. 26244793 PMC4862413 · DOI
  15. [16]Singh S, Nimse SB, Mathew DE, Dhimmar A, Sahastrabudhe H, Gajjar A, et al. Microbial melanin: recent advances in biosynthesis, extraction, characterization, and applications. Biotechnol Adv. 2021;53: 107773. 34022328 · DOI
  16. [17]Eisenman H, Nosanchuk J, Webber J, Emerson R, Camesano T, Casadevall A. Microstructure of cell wall-associated melanin in the human pathogenic fungus Cryptococcus neoformans. Biochemistry. 2005;44:3683–93. 15751945 · DOI
  17. [18]Chatterjee S, Prados-Rosales R, Tan S, Itin B, Casadevall A, Stark RE. Demonstration of a common indole-based aromatic core in natural and synthetic eumelanins by solid-state NMR. Org Biomol Chem. 2014;12:6730–6. 25047903 PMC4144758 · DOI
  18. [19]Raman NM, Ramasamy S. Genetic validation and spectroscopic detailing of DHN-melanin extracted from an environmental fungus. BB Rep. 2017;12:98–107. PMC5613234 28955797
  19. [20]Sun S, Zhang X, Sun S, Zhang L, Shan S, Zhu H. Production of natural melanin by Auricularia auricula and study on its molecular structure. Food Chem. 2016;190:801–7. 26213041 · DOI
  20. [21]Wakamatsu K, Ito S. Advanced chemical methods in melanin determination. Pigm Cell Res. 2002;15:174–83. 12028581 · DOI
  21. [22]Meredith P, Sarna T. The physical and chemical properties of eumelanin. Pigm Cell Res. 2006;19:572–94. 17083485 · DOI · Paper page
  22. [23]Karsili TNV, Marchetti B, Matsika S. Origins of Photodamage in pheomelanin constituents: photochemistry of 4-hydroxybenzothiazole. J Phys Chem A. 2018;122:1986–93. 29392956 · DOI
  23. [24]Micillo R, Panzella L, Koike K, Monfrecola G, Napolitano A, D’Ischia M. “Fifty shades” of black and red or how carboxyl groups fine tune eumelanin and pheomelanin properties. Int J Mol Sci. 2016;17:746. 27196900 PMC4881568 · DOI · Paper page
  24. [25]Cao W, Zhou X, McCallum NC, Hu Z, Ni QZ, Kapoor U, et al. Unraveling the structure and function of melanin through synthesis. J Am Chem Soc. 2021;143:2622–37. 33560127 · DOI
  25. [26]Turick CE, Knox AS, Becnel JM, Ekechukwu AA. Properties and function of pyomelanin. Biopolmers. 2010. 10.5772/10273. · DOI
  26. [27]Schmaler-Ripcke J, Sugareva V, Gebhardt P, Winkler R, Kniemeyer O, Heinekamp T, et al. Production of pyomelanin, a second type of melanin, via the tyrosine degradation pathway in Aspergillus fumigatus. Appl Environ Microbiol. 2009;75:493–503. 19028908 PMC2620705 · DOI
  27. [28]Kim E, Kang M, Tschirhart T, Malo M, Dadachova E, Cao G, et al. Spectroelectrochemical reverse engineering demonstrates that melanin’s redox and radical scavenging activities are linked. Biomacromol. 2017;18:4084–98. 29032671 · DOI
  28. [29]Nosanchuk JD, Stark RE, Casadevall A. Fungal melanin: what do we know about structure? Front Microbiol. 2015;6:1463. 26733993 PMC4687393 · DOI · Paper page
  29. [30]Pralea I-E, Moldovan R-C, Petrache A-M, Ilies M, Heghes S-C, Ielciu I, et al. From extraction to advanced analytical methods: the challenges of melanin analysis. Int J Mol Sci. 2019. 10.3390/ijms20163943. 31412656 PMC6719904 · DOI
  30. [32]Mostert AB, Hanson GR, Sarna T, Gentle IR, Powell BJ, Meredith P. Hydration-controlled X-band EPR spectroscopy: a tool for unravelling the complexities of the solid-state free radical in eumelanin. J Phys Chem B. 2013;117:4965–72. 23600769 · DOI
  31. [33]Chatterjee S, Prados-Rosales R, Frases S, Itin B, Casadevall A, Stark RE. Using solid-state NMR to monitor the molecular consequences of Cryptococcus neoformans melanization with different catecholamine precursors. Biochemistry. 2012;51:6080–8. 22765382 PMC3448835 · DOI
  32. [34]Tian S, Garcia-Rivera J, Yan B, Casadevall A, Stark RE. Unlocking the molecular structure of fungal melanin using 13c biosynthetic labeling and solid-state NMR. Biochemistry. 2003;42:8105–9. 12846559 · DOI
  33. [35]Almeida-Paes R, Frases S, Araújo GDS, de Oliveira MME, Gerfen GJ, Nosanchuk JD, et al. Biosynthesis and functions of a melanoid pigment produced by species of the Sporothrix complex in the presence of l-tyrosine. Appl Environ Microb. 2012;78:8623–30. PMC3502921 23042177 · DOI
  34. [36]Turick CE, Tisa LS, Caccavo F. Melanin production and use as a soluble electron shuttle for Fe(III) oxide reduction and as a terminal electron acceptor by Shewanella algae BrY. Appl Environ Microbiol. 2002;68:2436–44. 11976119 PMC127558 · DOI
  35. [37]Pihet M, Vandeputte P, Tronchin G, Renier G, Saulnier P, Georgeault S, et al. Melanin is an essential component for the integrity of the cell wall of Aspergillus fumigatus conidia. BMC Microbiol. 2009;9:177. 19703288 PMC2740851 · DOI · Paper page
  36. [38]Manini P, Lucci V, Lino V, Sartini S, Rossella F, Falco G, et al. Synthetic mycomelanin thin films as emergent bio-inspired interfaces controlling the fate of embryonic stem cells. J Mater Chem B. 2020;8:4412–8. 32373902 · DOI
  37. [39]Sun S, Zhang X, Chen W, Zhang L, Zhu H. Production of natural edible melanin by Auricularia auricula and its physicochemical properties. Food Chem. 2016;196:486–92. 26593518 · DOI
  38. [40]Helan M, Mi HSR, Thangavelu R, Subramanian J, Kalaiselvam M. Production and characterization of melanin pigment from halophilic black yeast Hortaea werneckii. Int J Pharm Res Rev. 2013;2:9–17.
  39. [41]Zhang Y, Wu X, Huang C, Zhang Z, Gao W. Isolation and identification of pigments from oyster mushrooms with black, yellow and pink caps. Food Chem. 2022;372: 131171. 34601416 · DOI
  40. [42]Babitskaya VG, Shcherba VV, Filimonova TV, Grigorchuk EA. Melanin pigments from the fungi Paecilomyces variotii and Aspergillus carbonarius. Appl Biochem Microbiol. 2000;36:128–33. 10780001 · DOI
  41. [43]Ribera J, Panzarasa G, Stobbe A, Osypova A, Rupper P, Klose D, et al. Scalable biosynthesis of melanin by the basidiomycete Armillaria cepistipes. J Agric Food Chem. 2019;67:132–9. 30541276 · DOI
  42. [44]Tran-Ly A, Reyes C, Schwarze F, Ribera J. Microbial production of melanin and its various applications. World J Microb Biot. 2020. 10.1007/s11274-020-02941-z. PMC7548279 33043393 · DOI
  43. [45]Akilandeswari P, Pradeep BV. Exploration of industrially important pigments from soil fungi. Appl Microbiol Biotechnol. 2016;100:1631–43. 26701360 · DOI
  44. [46]Carreira A, Ferreira LM, Loureiro V. Production of brown tyrosine pigments by the yeast Yarrowia lipolytica. J Appl Microbiol. 2001;90:372–9. 11298232 · DOI
  45. [47]Ma Z, Liu X, Liu Y, Chen W, Wang C. Studies on the biosynthetic pathways of melanin in Auricularia auricula. J Basic Microbiol. 2022;62:843–56. 35419841 · DOI
  46. [48]Zou Y, Tian M. Fermentative production of melanin by Auricularia auricula. J Food Process Pres. 2017;41: e12909. · DOI
  47. [49]Velmurugan P, Hur H, Balachandar V, Kamala-Kannan S, Lee K-J, Lee S-M, et al. Monascus pigment production by solid-state fermentation with corn cob substrate. J Biosci Bioeng. 2011;112:590–4. 21906997 · DOI
  48. [50]Silveira ST, Daroit DJ, Brandelli A. Pigment production by Monascus purpureus in grape waste using factorial design. LWT-Food Sci Technol. 2008;41:170–4. · DOI
  49. [51]Aghajanyan AE, Hambardzumyan AA, Minasyan EV, Tsaturyan AH, Paloyan AM, Avetisyan SV, et al. Development of the technology for producing water-soluble melanin from waste of vinary production and the study of its physicochemical properties. Eur Food Res Technol. 2022;248:485–95. · DOI
  50. [53]Said F, Chisti Y, Brooks J. The effects of forced aeration and initial moisturelevel on red pigment and biomass production by Monascus ruber in packed bed solid state fermentation. J Int Environ Appl Sci. 2010;1:1–4.
  51. [54]Velmurugan P, Lee YH, Venil CK, Lakshmanaperumalsamy P, Chae J-C, Oh B-T. Effect of light on growth, intracellular and extracellular pigment production by five pigment-producing filamentous fungi in synthetic medium. J Biosci Bioeng. 2010;109:346–50. 20226375 · DOI
  52. [55]Vendruscolo F, Bühler RMM, de Carvalho JC, de Oliveira D, Moritz DE, Schmidell W, et al. Monascus: a reality on the production and application of microbial pigments. Appl Biochem Biotechnol. 2016;178:211–23. 26472672 · DOI
  53. [56]Zhang M, Xiao G, Thring RW, Chen W, Zhou H, Yang H. Production and characterization of melanin by submerged culture of culinary and medicinal fungi Auricularia auricula. Appl Biochem Biotechnol. 2015;176:253–66. 25800528 · DOI
  54. [57]Chávez-Béjar MI, Lara AR, López H, Hernández-Chávez G, Martinez A, Ramírez OT, et al. Metabolic engineering of escherichia coli for l-tyrosine production by expression of genes coding for the chorismate mutase domain of the native chorismate mutase-prephenate dehydratase and a cyclohexadienyl dehydrogenase from Zymomonas mobilis. Appl Environ Microbiol. 2008;74:3284–90. 18344329 PMC2394925 · DOI
  55. [58]Ben Tahar I, Kus-Liskiewicz M, Lara Y, Javaux E, Fickers P. Characterization of a nontoxic pyomelanin pigment produced by the yeast Yarrowia lipolytica. Biotechnol Progr. 2020;36. 10.1002/btpr.2912. 31525285 · DOI
  56. [60]Li Z, Heng H, Qin Q, Chen L, Wang Y, Zhou Z. Physicochemical properties, molecular structure, antioxidant activity, and biological function of extracellular melanin from Ascosphaera apis. J Zhejiang Univ Sci B. 2022;23:365–81. 35557038 PMC9110319 · DOI
  57. [61]Zou Y, Xie C, Fan G, Gu Z, Han Y. Optimization of ultrasound-assisted extraction of melanin from Auricularia auricula fruit bodies. Innov Food Sci Emerg. 2010;11:611–5. · DOI
  58. [62]Zhang F, Xue F, Xu H, Yuan Y, Wu X, Zhang J, et al. Optimization of solid-state fermentation extraction of inonotus hispidus fruiting body melanin. Foods. 2021;10(12):2893. 34945444 PMC8700211 · DOI
  59. [63]Quan Y, van den Ende BG, Shi D, Prenafeta-Boldú FX, Liu Z, Al-Hatmi AMS, et al. A comparison of isolation methods for black fungi degrading aromatic toxins. Mycopathologia. 2019;184:653–60. 31565783 · DOI
  60. [64]Raman NM, Shah PH, Mohan M, Ramasamy S. Improved production of melanin from Aspergillus fumigatus AFGRD105 by optimization of media factors. AMB Express. 2015;5:72. 26597959 PMC4656259 · DOI
  61. [65]Medeiros WB, Medina KJD, Sponchiado SRP. Improved natural melanin production by Aspergillus nidulans after optimization of factors involved in the pigment biosynthesis pathway. Microb Cell Fact. 2022;21:278. 36585654 PMC9801647 · DOI
  62. [66]Rudrappa M, Kumar M, Kumar R, Almansour A, Perumal K, Nayaka S. Bioproduction, purification and physicochemical characterization of melanin from Streptomyces sp. strain MR28. Microbiol Res. 2022. 10.1016/j.micres.2022.127130. 35870343 · DOI
  63. [67]Morris-Jones R, Gomez BL, Diez S, Uran M, Morris-Jones SD, Casadevall A, et al. Synthesis of melanin pigment by Candida albicans in vitro and during infection. Infect Immun. 2005;73:6147–50. 16113337 PMC1231073 · DOI
  64. [68]Baker R, Chrissian C, Stark R, Casadevall A. Cryptococcus neoformans melanization incorporates multiple catecholamines to produce polytypic melanin. J Biol Chem. 2022. 10.1016/j.jbc.2021.101519. 34942148 PMC8760516 · DOI
  65. [69]Wheeler MH. Comparisons of fungal melanin biosynthesis in ascomycetous, imperfect and basidiomycetous fungi. Trans Br Mycol Soc. 1983;81:29–36. · DOI · Paper page
  66. [70]Funa N, Ohnishi Y, Fujii I, Shibuya M, Ebizuka Y, Horinouchi S. A new pathway for polyketide synthesis in microorganisms. Nature. 1999;400:897–9. 10476972 · DOI
  67. [71]Wheeler MH, Bell AA. Melanins and their importance in pathogenic fungi. Curr Top Med Mycol. 1988;2:338–87. 3288360 · DOI
  68. [72]Gao J, Wenderoth M, Doppler M, Schuhmacher R, Marko D, Fischer R. Fungal melanin biosynthesis pathway as source for fungal toxins. MBIO. 2022;13:e0021922. 35475649 PMC9239091 · DOI
  69. [73]Walton FJ, Idnurm A, Heitman J. Novel gene functions required for melanization of the human pathogen Cryptococcus neoformans. Mol Microbiol. 2005;57:1381–96. 16102007 · DOI
  70. [74]Zhou S, Zhang P, Zhou H, Liu X, Li S-M, Guo L, et al. A new regulator RsdA mediating fungal secondary metabolism has a detrimental impact on asexual development in Pestalotiopsis fici. Environ Microbiol. 2019;21:416–26. 30421486 · DOI
  71. [75]Cohrs KC, Simon A, Viaud M, Schumacher J. Light governs asexual differentiation in the grey mould fungus Botrytis cinerea via the putative transcription factor BcLTF2. Environ Microbiol. 2016;18:4068–86. 27347834 · DOI
  72. [76]Gao P, Jin K, Xia Y. The phosphatase gene MaCdc14 negatively regulates UV-B tolerance by mediating the transcription of melanin synthesis-related genes and contributes to conidiation in Metarhizium acridum. Curr Genet. 2020;66:141–53. 31256233 · DOI
  73. [77]Chang P-K, Cary JW, Lebar MD. Biosynthesis of conidial and sclerotial pigments in Aspergillus species. Appl Microbiol Biotechnol. 2020;104:2277–86. 31974722 · DOI
  74. [78]Feng B, Wang X, Hauser M, Kaufmann S, Jentsch S, Haase G, et al. Molecular cloning and characterization of wdpks1, a gene involved in dihydroxynaphthalene melanin biosynthesis and virulence in Wangiella (Exophiala) dermatitidis. Infect Immun. 2001;69:1781–94. 11179356 PMC98085 · DOI
  75. [79]Zhang C, He Y, Zhu P, Chen L, Wang Y, Ni B, et al. Loss of bcbrn1 and bcpks13 in Botrytis cinerea not only blocks melanization but also increases vegetative growth and virulence. Mol Plant-Microbe Interact. 2015;28:1091–101. 26035129 · DOI · Paper page
  76. [80]Takano Y, Kubo Y, Shimizu K, Mise K, Okuno T, Furusawa I. Structural analysis of PKS1, a polyketide synthase gene involved in melanin biosynthesis in Colletotrichum lagenarium. Mol Gen Genet. 1995;249:162–7. 7500937 · DOI
  77. [81]Woo PCY, Tam EWT, Chong KTK, Cai JJ, Tung ETK, Ngan AHY, et al. High diversity of polyketide synthase genes and the melanin biosynthesis gene cluster in Penicillium marneffei. FEBS J. 2010;277:3750–8. 20718860 · DOI
  78. [82]Fan R, Klosterman SJ, Wang C, Subbarao KV, Xu X, Shang W, et al. Vayg1 is required for microsclerotium formation and melanin production in Verticillium dahliae. Fungal Genet Biol. 2017;98:1–11. 27866941 · DOI
  79. [83]Perpetua NS, Kubo Y, Takano Y, Furusawa I. Cloning and characterization of a melanin biosynthetic THR1 reductase gene essential for appressorial penetration of Colletotrichum lagenarium. Mol Plant-Microbe Interact. 1996;9:323–9. 8672814 · DOI
  80. [84]Kubo Y, Takano Y, Endo N, Yasuda N, Tajima S, Furusawa I. Cloning and structural analysis of the melanin biosynthesis gene SCD1 encoding scytalone dehydratase in Colletotrichum lagenarium. Appl Environ Microb. 1996;62:4340–4. PMC168262 8953707 · DOI
  81. [85]Pukkila-Worley R, Gerrald Q, Kraus P, Boily M, Davis M, Giles S, et al. Transcriptional network of multiple capsule and melanin genes governed by the Cryptococcus neoformans cyclic AMP cascade. Eukaryot Cell. 2005;4:190–201. 15643074 PMC544166 · DOI
  82. [86]Perez-Cuesta U, Aparicio-Fernandez L, Guruceaga X, Martin-Souto L, Abad-Diaz-de-Cerio A, Antoran A, et al. Melanin and pyomelanin in Aspergillus fumigatus: from its genetics to host interaction. Int Microbiol. 2020;23:55–63. 31020477 · DOI
  83. [87]Keller S, Macheleidt J, Scherlach K, Schmaler-Ripcke J, Jacobsen ID, Heinekamp T, et al. Pyomelanin formation in Aspergillus fumigatus requires hmgx and the transcriptional activator hmgr but is dispensable for virulence. PLoS ONE. 2011;6: e26604. 22046314 PMC3203155 · DOI
  84. [88]Pal AK, Gajjar DU, Vasavada AR. DOPA and DHN pathway orchestrate melanin synthesis in Aspergillus species. Med Mycol. 2014;52:10–8. 23998343
  85. [89]Woloshuk CP, Sisler HD, Tokousbalides MC, Dutky SR. Melanin biosynthesis in Pyricularia oryzae: site of tricyclazole inhibition and pathogenicity of melanin-deficient mutants. Pestic Biochem Phys. 1980;14:256–64. · DOI
  86. [90]Youngchim S, Morris-Jones R, Hay RJ, Hamilton AJ. Production of melanin by Aspergillus fumigatus. J Med Microbiol. 2004;53:175–81. 14970241 · DOI
  87. [91]Langfelder K, Streibel M, Jahn B, Haase G, Brakhage AA. Biosynthesis of fungal melanins and their importance for human pathogenic fungi. Fungal Genet Biol. 2003;38:143–58. 12620252 · DOI · Paper page
  88. [92]Ngamskulrungroj P, Himmelreich U, Breger JA, Wilson C, Chayakulkeeree M, Krockenberger MB, et al. The trehalose synthesis pathway is an integral part of the virulence composite for Cryptococcus gattii. Infect Immun. 2009;77:4584–96. 19651856 PMC2747965 · DOI
  89. [93]Baraboi VA. Melanin: structure, biosynthesis, biological functions. Ukrains’kyi biokhimichnyi zhurnal. 1999;1999(71):5–14. 10791050
  90. [94]Eisenman HC, Casadevall A. Synthesis and assembly of fungal melanin. Appl Microbiol Biotechnol. 2012;93:931–40. 22173481 PMC4318813 · DOI · Paper page
  91. [96]Schumacher J. DHN melanin biosynthesis in the plant pathogenic fungus Botrytis cinerea is based on two developmentally regulated key enzyme (PKS)-encoding genes. Mol Microbiol. 2016;99:729–48. 26514268 · DOI · Paper page
  92. [97]Heinekamp T, Thywissen A, Macheleidt J, Keller S, Valiante V, Brakhage AA. Aspergillus fumigatus melanins: interference with the host endocytosis pathway and impact on virulence. Front Microbiol. 2013;3:440. 23346079 PMC3548413 · DOI · Paper page
  93. [98]Weijn A, Bastiaan-Net S, Wichers HJ, Mes JJ. Melanin biosynthesis pathway in Agaricus bisporus mushrooms. Fungal Genet Biol. 2013;55:42–53. 23123422 · DOI
  94. [99]Geib E, Gressler M, Viediernikova I, Hillmann F, Jacobsen ID, Nietzsche S, et al. A non-canonical melanin biosynthesis pathway protects Aspergillus terreus conidia from environmental stress. Cell Chem Biol. 2016;23:587–97. 27133313 · DOI
  95. [100]Raposo G, Marks MS. Melanosomes—dark organelles enlighten endosomal membrane transport. Nat Rev Mol Cell Biol. 2007;8:786–97. 17878918 PMC2786984 · DOI
  96. [101]Maranduca MA, Branisteanu D, Serban DN, Branisteanu DC, Stoleriu G, Manolache N, et al. Synthesis and physiological implications of melanic pigments. Oncol Lett. 2019;17:4183–7. 30944614 PMC6444329
  97. [102]Wu X, Hammer JA. Melanosome transfer: it is best to give and receive. Curr Opin Cell Biol. 2014;29:1–7. 24662021 PMC4130791 · DOI
  98. [103]Walker CA, Gómez BL, Mora-Montes HM, Mackenzie KS, Munro CA, Brown AJP, et al. Melanin externalization in Candida albicans depends on cell wall chitin structures. Eukaryot Cell. 2010;9:1329–42. 20543065 PMC2937336 · DOI
  99. [104]Garcia-Rubio R, de Oliveira H, Rivera J, Trevijano-Contador N. The fungal cell wall: Candida, Cryptococcus, and Aspergillus species. Front Microbiol. 2020;10:2993. 31993032 PMC6962315 · DOI · Paper page
  100. [105]Hwang DS, Masic A, Prajatelistia E, Iordachescu M, Waite JH. Marine hydroid perisarc: a chitin- and melanin-reinforced composite with DOPA–iron(III) complexes. Acta Biomater. 2013;9:8110–7. 23791678 · DOI
  101. [106]Tsirilakis K, Kim C, Vicencio AG, Andrade C, Casadevall A, Goldman DL. Methylxanthine inhibit fungal chitinases and exhibit antifungal activity. Mycopathologia. 2012;173:83–91. 21968902 PMC4289597 · DOI
  102. [107]Upadhyay S, Xu X, Lowry D, Jackson JC, Roberson RW, Lin X. Subcellular compartmentalization and trafficking of the biosynthetic machinery for fungal melanin. Cell Rep. 2016;14:2511–8. 26972005 PMC4805463 · DOI
  103. [108]Lee D, Jang E, Lee M, Kim S, Lee Y, Lee K, et al. Unraveling melanin biosynthesis and signaling networks in Cryptococcus neoformans. MBio. 2019. 10.1128/mBio.02267-19. 31575776 PMC6775464 · DOI
  104. [109]Yamamoto K, Tatebayashi K, Saito H. Binding of the extracellular eight-cysteine motif of Opy2 to the putative osmosensor Msb2 is essential for activation of the yeast high-osmolarity glycerol pathway. Mol Cell Biol. 2016;36:475–87. 26598606 PMC4719420 · DOI
  105. [110]Ren W, Liu N, Yang Y, Yang Q, Chen C, Gao Q. The sensor proteins BcSho1 and BcSln1 are involved in, though not essential to, vegetative differentiation, pathogenicity and osmotic stress tolerance in Botrytis cinerea. Front Microbiol. 2019;10:328. 30858841 PMC6397835 · DOI
  106. [111]de Nadal E, Posas F. The HOG pathway and the regulation of osmoadaptive responses in yeast. Fems Yeast Res. 2022;22:foac13. PMC8953452 35254447
  107. [112]Saputo S, Chabrier-Rosello Y, Luca FC, Kumar A, Krysan DJ. The RAM network in pathogenic fungi. Eukaryot Cell. 2012;11:708–17. 22544903 PMC3370468 · DOI · Paper page
  108. [113]Panepinto J, Liu L, Ramos J, Zhu X, Valyi-Nagy T, Eksi S, et al. The DEAD-box RNA helicase Vad1 regulates multiple virulence-associated genes in Cryptococcus neoformans. J Clin Invest. 2005;115:632–41. 15765146 PMC1051994 · DOI
  109. [114]Erickson T, Liu L, Gueyikian A, Zhu X, Gibbons J, Williamson PR. Multiple virulence factors of Cryptococcus neoformans are dependent on VPH1. Mol Microbiol. 2001;42:1121–31. 11737651 · DOI
  110. [115]Idnurm A, Reedy JL, Nussbaum JC, Heitman J. Cryptococcus neoformans virulence gene discovery through insertional mutagenesis. Eukaryot Cell. 2004;3:420–9. 15075272 PMC387659 · DOI
  111. [116]Caza M, Kronstad JW. The camp/protein kinase a pathway regulates virulence and adaptation to host conditions in Cryptococcus neoformans. Front Cell Infect Mi. 2019;9:212. PMC6592070 31275865 · DOI
  112. [117]Alspaugh JA, Perfect JR, Heitman J. Cryptococcus neoformans mating and virulence are regulated by the G-protein alpha subunit GPA1 and cAMP. Genes Dev. 1997;11:3206–17. 9389652 PMC316752 · DOI
  113. [118]Bahn YS, Hicks JK, Giles SS, Cox GM, Heitman J. Adenylyl cyclase-associated protein Aca1 regulates virulence and differentiation of Cryptococcus neoformans via the cyclic AMP protein kinase A cascade. Eukaryot Cell. 2004;3:1476–91. 15590822 PMC539029 · DOI
  114. [119]Heung LJ, Kaiser AE, Luberto C, Poeta MD. The role and mechanism of diacylglycerol-protein kinase C1 signaling in melanogenesis by Cryptococcus neoformans *. J Biol Chem. 2005;280:28547–55. 15946943 · DOI
  115. [120]Shuangli T, Jie W, Shasha L, Junjun S. Deletion and functional studies of SER5 gene in Cryptococcus neoformans. Chin J Mycol. 2021;16:335–40.
  116. [121]Zhu X, Williamson P. Role of laccase in the biology and virulence of Cryptococcus neoformans. Fems Yeast Res. 2004;5:1–10. 15381117 · DOI
  117. [122]Samantaray S, Neubauer M, Helmschrott C, Wagener J. Role of the guanine nucleotide exchange factor Rom2 in cell wall integrity maintenance of Aspergillus fumigatus. Eukaryot Cell. 2013;12:288–98. 23264643 PMC3571289 · DOI
  118. [123]Valiante V, Jain R, Heinekamp T, Brakhage AA. The MpkA MAP kinase module regulates cell wall integrity signaling and pyomelanin formation in Aspergillus fumigatus. Fungal Genet Biol. 2009;46:909–18. 19715768 · DOI
  119. [124]Yaakoub H, Sanchez N, Ongay-Larios L, Courdavault V, Calenda A, Bouchara J, et al. The high osmolarity glycerol (HOG) pathway in fungi (dagger). Crit Rev Microbiol. 2022;48:657–95. 34893006 · DOI
  120. [125]Bahn YS, Kojima K, Cox GM, Heitman J. Specialization of the HOG pathway and its impact on differentiation and virulence of Cryptococcus neoformans. Mol Biol Cell. 2005;16:2285–300. 15728721 PMC1087235 · DOI
  121. [126]Kojima K, Bahn YS, Heitman J. Calcineurin, Mpk1 and Hog1 MAPK pathways independently control fludioxonil antifungal sensitivity in Cryptococcus neoformans. Microbiology (UK). 2006;152:591–604. 16514140 · DOI
  122. [127]Du Y, Jin K, Xia Y. Involvement of MaSom1, a downstream transcriptional factor of cAMP/PKA pathway, in conidial yield, stress tolerances, and virulence in Metarhizium acridum. Appl Microbiol Biotechnol. 2018;102:5611–23. 29713793 · DOI
  123. [128]Song D, Cao Y, Xia Y. Transcription factor MaMsn2 regulates conidiation pattern shift under the control of mah1 through homeobox domain in Metarhizium acridum. JoF. 2021;7:840. 34682261 PMC8541488 · DOI
  124. [129]Williamson PR. Biochemical and molecular characterization of the diphenol oxidase of Cryptococcus neoformans: identification as a laccase. J Bacteriol. 1994;176:656–64. 8300520 PMC205102 · DOI
  125. [130]Zhang P, Wei D, Li Z, Sun Z, Pan J, Zhu X. Cryptococcal phosphoglucose isomerase is required for virulence factor production, cell wall integrity and stress resistance. Fems Yeast Res. 2015;15(7):fov072. 26271120 · DOI
  126. [131]Manap ASA, Lum YK, Ong LH, Tang Y-Q, Gew LT, Chia AYY. Perspective approaches on melanogenesis inhibition. Dermatol Sin. 2021;39:1. · DOI
  127. [132]Zolghadri S, Bahrami A, Hassan Khan MT, Munoz-Munoz J, Garcia-Molina F, Garcia-Canovas F, et al. A comprehensive review on tyrosinase inhibitors. J Enzym Inhib Med Ch. 2019;34:279–309. PMC6327992 30734608 · DOI
  128. [133]Freitas DF, da Rocha IM, Vieira-da-Motta O, de Paula SC. The role of melanin in the biology and ecology of Nematophagous fungi. J Chem Ecol. 2021;47:597–613. 34232439 · DOI
  129. [134]Zeng G, Zhang P, Zhang Q, Zhao H, Li Z, Zhang X, et al. Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species. PLoS Genet. 2018;14: e1007472. 29958281 PMC6042797 · DOI
  130. [135]Jung K-W, Yang D-H, Maeng S, Lee K-T, So Y-S, Hong J, et al. Systematic functional profiling of transcription factor networks in Cryptococcus neoformans. Nat Commun. 2015;6:6757. 25849373 PMC4391232 · DOI
  131. [136]Jia S-L, Chi Z, Chen L, Liu G-L, Hu Z, Chi Z-M. Molecular evolution and regulation of DHN melanin-related gene clusters are closely related to adaptation of different melanin-producing fungi. Genomics. 2021;113:1962–75. 33901575 · DOI
  132. [137]Cho Y, Srivastava A, Ohm RA, Lawrence CB, Wang K-H, Grigoriev IV, et al. Transcription factor Amr1 induces melanin biosynthesis and suppresses virulence in Alternaria brassicicola. PLoS Pathog. 2012;8: e1002974. 23133370 PMC3486909 · DOI · Paper page
  133. [138]Wang Y, Hu X, Fang Y, Anchieta A, Goldman PH, Hernandez G, et al. Transcription factor VdCmr1 is required for pigment production, protection from UV irradiation, and regulates expression of melanin biosynthetic genes in Verticillium dahliae. Microbiology (UK). 2018;164:863–4. PMC5982140 29485393 · DOI
  134. [139]Zhou Y, Yang L, Wu M, Chen W, Li G, Zhang J. A single-nucleotide deletion in the transcription factor gene bcsmr1 causes sclerotial-melanogenesis deficiency in Botrytis cinerea. Front Microbiol. 2017;8:2492. 29312200 PMC5733056 · DOI
  135. [140]Zhang Z, Jia H, Liu N, Li H, Meng Q, Wu N, et al. The zinc finger protein StMR1 affects the pathogenicity and melanin synthesis of Setosphaeria turcica and directly regulates the expression of DHN melanin synthesis pathway genes. Mol Microbiol. 2022;117:261–73. 34278632 · DOI · Paper page
  136. [141]Zhou M, Li Z, Liu Y, Zhang P, Hao X, Zhu X. Transcription factors Pmr1 and Pmr2 cooperatively regulate melanin biosynthesis, conidia development and secondary metabolism in Pestalotiopsis microspora. JoF. 2022;8(1):38. PMC8781371 35049978 · DOI
  137. [142]Valiante V, Baldin C, Hortschansky P, Jain R, Thywissen A, Strassburger M, et al. The Aspergillus fumigatus conidial melanin production is regulated by the bifunctional bHLH DevR and MADS-box RlmA transcription factors. Mol Microbiol. 2016;102:321–35. 27393422 · DOI
  138. [143]Zhang P, Zhou S, Wa G, An Z, Liu X, Li K, et al. Two transcription factors cooperatively regulate DHN melanin biosynthesis and development in Pestalotiopsis fici. Mol Microbiol. 2019;112:649–66. 31116900 · DOI · Paper page
  139. [144]Bailey LA, Ebbole DJ. The fluffy gene of Neurospora crassa encodes a gal4p-type C6 zinc cluster protein required for conidial development. Genetics. 1998;148:1813–20. 9560395 PMC1460068 · DOI
  140. [145]Lee S, Völz R, Song H, Harris W, Lee Y-H. Characterization of the MYB genes reveals insights into their evolutionary conservation, structural diversity, and functional roles in Magnaporthe oryzae. Front Microbiol. 2021;12: 721530. 34899620 PMC8660761 · DOI
  141. [146]Li C, Xia Y, Jin K. N-terminal zinc fingers of MaNCP1 contribute to growth, stress tolerance, and virulence in Metarhizium acridum. Int J Biol Macromol. 2022;216:426–36. 35809667 · DOI
  142. [147]Song D, Shi Y, Ji H, Xia Y, Peng G. The MaCreA gene regulates normal conidiation and microcycle conidiation in Metarhizium acridum. Front Microbiol. 2019;10:1946. 31497008 PMC6713048 · DOI
  143. [148]Su X, Liu H, Xia Y, Cao Y. Transcription Factor Mavib-1 negatively regulates conidiation by affecting utilization of carbon and nitrogen source in Metarhizium acridum. JoF. 2022;8(1):594. 35736077 PMC9224900 · DOI
  144. [149]Song L, Xue X, Wang S, Li J, Jin K, Xia Y. MaAts, an alkylsulfatase, contributes to fungal tolerances against UV-B irradiation and heat-shock in Metarhizium acridum. JoF. 2022;8(3):270. 35330272 PMC8951457 · DOI
  145. [150]Song D, Cao Y, Xia Y. MaNsdD regulates conidiation negatively by inhibiting the AbaA expression required for normal conidiation in Metarhizium acridum. Environ Microbiol. 2022;24:2951–61. 35384250 · DOI
  146. [151]Su X, Yan X, Chen X, Guo M, Xia Y, Cao Y. Calcofluor white hypersensitive proteins contribute to stress tolerance and pathogenicity in entomopathogenic fungus, Metarhizium acridum. Pest Manag Sci. 2021;77:1915–24. 33300230 · DOI
  147. [152]Wang J, Wang Q, Huang P, Qu Y, Huang Z, Wang H, et al. An appressorium membrane protein, Pams1, controls infection structure maturation and virulence via maintaining endosomal stability in the rice blast fungus. Front Plant Sci. 2022;13: 955254. 36160954 PMC9500233 · DOI
  148. [153]Choi K-Y. Bioprocess of microbial melanin production and isolation. Front Bioeng Biotech. 2021;9: 765110. PMC8637283 34869277 · DOI
  149. [154]Martínez LM, Martinez A, Gosset G. Production of melanins with recombinant microorganisms. Front Bioeng Biotech. 2019;7:285. PMC6821874 31709247 · DOI
  150. [155]Halaouli S, Record E, Casalot L, Hamdi M, Sigoillot J-C, Asther M, et al. Cloning and characterization of a tyrosinase gene from the white-rot fungus Pycnoporus sanguineus, and overproduction of the recombinant protein in Aspergillus niger. Appl Microbiol Biotechnol. 2006;70:580–9. 16151802 · DOI
  151. [156]Lee H, Choi J, Kwon S, Park E, Oh B, Kim J, et al. Melanin biopolymer synthesis using a new melanogenic strain of Flavobacterium kingsejongi and a recombinant strain of Escherichia coli expressing 4-hydroxyphenylpyruvate dioxygenase from F. kingsejongi. Microb Cell Fact. 2022;21(1):75. 35501871 PMC9063278 · DOI
  152. [157]Kihara J, Moriwaki A, Tanaka N, Tanaka C, Ueno M, Arase S. Characterization of the BMR1 gene encoding a transcription factor for melanin biosynthesis genes in the phytopathogenic fungus Bipolaris oryzae. Fems Microbiol Lett. 2008;281:221–7. 18312572 · DOI
  153. [158]Mavridi-Printezi A, Menichetti A, Guernelli M, Montalti M. The photophysics and photochemistry of melanin-like nanomaterials depend on morphology and structure. Chem Eur J. 2021;27:16309–19. 34505731 PMC9291563 · DOI
  154. [159]Li S, Yang L, Li J, Chen T, Ye M. Structure, molecular modification, and anti-radiation activity of melanin from Lachnum YM156 on ultraviolet b-induced injury in mice. Appl Biochem Biotechnol. 2019;188:555–67. 30547280 · DOI
  155. [160]Zhou X, Su S, Vanthournout B, Hu Z, Son FA, Zhang K, et al. Hydrophobic melanin via post-synthetic modification for controlled self-assembly. ACS Nano. 2022;16:19087–95. 36343336 · DOI
  156. [161]Liu R, Meng X, Mo C, Wei X, Ma A. Melanin of fungi: from classification to application. World J Microbiol Biotechnol. 2022;38:228. 36149606 · DOI
  157. [162]Sarna T, Swartz HM, Zadlo A. Interaction of melanin with metal ions modulates their cytotoxic potential. Appl Magn Reson. 2022;53:105–21. · DOI
  158. [163]Prenafeta-Boldú FX, Roca N, Villatoro C, Vera L, de Hoog GS. Prospective application of melanized fungi for the biofiltration of indoor air in closed bioregenerative systems. J Hazard Mater. 2019;361:1–9. 30176406 · DOI
  159. [164]Anh N, Ribera J, Schwarze F, Brunelli M, Fortunato G. Fungal melanin-based electrospun membranes for heavy metal detoxification of water. Sustain Mater Technol. 2020. 10.1016/j.susmat.2019.e00146. · DOI
  160. [165]Lamia K, N’ji G. Aspergillus niger is able to decolourize sepia ink contained in saline industrial wastewaters. Desalin Water Treat. 2010;20:144–53. · DOI
  161. [166]Jeon J-R, Le TT, Chang Y-S. Dihydroxynaphthalene-based mimicry of fungal melanogenesis for multifunctional coatings. Microb Biotechnol. 2016;9:305–15. 26833568 PMC4835569 · DOI
  162. [167]Wu X, Fang L-Z, Liu F-L, Pang X-J, Qin H-L, Zhao T, et al. New prenylxanthones, polyketide hemiterpenoid pigments from the endophytic fungus Emericella sp. XL029 and their anti-agricultural pathogenic fungal and antibacterial activities. RSC Adv. 2017;7:31115–22. · DOI
  163. [168]Cordero RJB. Melanin for space travel radioprotection. Environ Microbiol. 2017;19:2529–32. 28419675 · DOI
  164. [169]Rong L, Zhang Y, Li W-S, Su Z, Fadhil JI, Zhang C. Iron chelated melanin-like nanoparticles for tumor-associated macrophage repolarization and cancer therapy. Biomaterials. 2019;225: 119515. 31590119 · DOI
  165. [170]Marcovici I, Coricovac D, Pinzaru I, Macasoi IG, Popescu R, Chioibas R, et al. Melanin and melanin-functionalized nanoparticles as promising tools in cancer research—a review. Cancers. 2022;14:1838. 35406610 PMC8998143 · DOI
  166. [171]Mavridi-Printezi A, Guernelli M, Menichetti A, Montalti M. Bio-applications of multifunctional melanin nanoparticles: from nanomedicine to nanocosmetics. Nanomaterials. 2020;10:2276. 33212974 PMC7698489 · DOI
  167. [172]Shi F, Li J, Yang L, Hou G, Ye M. Hypolipidemic effect and protection ability of liver-kidney functions of melanin from Lachnum YM226 in high-fat diet fed mice. Food Funct. 2018;9:880–9. 29299589 · DOI
  168. [173]Hou R, Liu X, Wu X, Zheng M, Fu J. Therapeutic effect of natural melanin from edible fungus Auricularia auricula on alcohol-induced liver damage in vitro and in vivo. Food Sci Human Wellness. 2021;10:514–22. · DOI
  169. [174]Lim W, Konings M, Parel F, Eadie K, Strepis N, Fahal A, et al. Inhibiting DHN- and DOPA-melanin biosynthesis pathway increased the therapeutic value of itraconazole in Madurella mycetomatis infected Galleria mellonella. Med Mycol. 2022;60:myac003. 35064672 PMC9295015 · DOI
  170. [175]Tokousbalides M, Sisler H. Site of inhibition by tricyclazole in the melanin biosynthetic-pathway of Verticillium-Dahliae. Pest Biochem Physiol. 1979;11:64–73. · DOI
  171. [176]Oliveira L, Ferrarini M, dos Santos A, Varela M, Correa I, Tempone A, et al. Coumaric acid analogues inhibit growth and melanin biosynthesis in Cryptococcus neoformans and potentialize amphotericin B antifungal activity. Eur J Pharm Sci. 2020. 10.1016/j.ejps.2020.105473. 32693012 · DOI
  172. [177]Azam F, Khan MA, Khan A, Ahmad S, Zofair SFF, Younus H. In silico and in vitro studies on the inhibition of laccase activity by ellagic acid: implications in drug designing for the treatment of Cryptococcal infections. Int J Biol Macromol. 2022;209:642–54. 35421416 · DOI
  173. [178]Castelo-Branco DdSCM, da Rocha MG, de Oliveira JS, Araujo GdS, Martins DV, Garcia LGS, et al. The herbicide paraquat alters growth and melanin production on the Cryptococcus neoformans / Cryptococcus gattii species complex. Can J Microbiol. 2022;68:493–9. 35303412
  174. [179]Geib E, Brock M. Comment on: “Melanisation of Aspergillus terreus -is butyrolactone i involved in the regulation of both DOPA and DHN types of pigments in submerged culture? Microorganisms 2017, 5, 22”. Microorganisms. 2017;5:34. 28635676 PMC5488105 · DOI
  175. [180]Casadevall A, Cordero RJB, Bryan R, Nosanchuk J, Dadachova E. Melanin, radiation, and energy transduction in fungi. Microbiol Spectr. 2017;5:FUNK-0037-2016. PMC11687467 28256187 · DOI · Paper page
  176. [181]Ambrico M, Ambrico PF, Ligonzo T, Cardone A, Cicco SR, d’Ischia M, et al. From commercial tyrosine polymers to a tailored polydopamine platform: concepts, issues and challenges en route to melanin-based bioelectronics. J Mater Chem C. 2015;3:6413–23. · DOI
  177. [182]Mostert AB, Powell BJ, Pratt FL, Hanson GR, Sarna T, Gentle IR, et al. Role of semiconductivity and ion transport in the electrical conduction of melanin. Proc Natl Acad Sci. 2012;109:8943–7. 22615355 PMC3384144 · DOI
  178. [183]Bothma JP, de Boor J, Divakar U, Schwenn PE, Meredith P. Device-quality electrically conducting melanin thin films. Adv Mater. 2008;20:3539–42. · DOI
  179. [184]Kim YJ, Wu W, Chun S-E, Whitacre JF, Bettinger CJ. Biologically derived melanin electrodes in aqueous sodium-ion energy storage devices. PNAS. 2013;110:20912–7. 24324163 PMC3876213 · DOI
  180. [185]Venil C, Velmurugan P, Dufosse L, Devi P, Ravi A. Fungal pigments: potential coloring compounds for wide ranging applications in textile dyeing. JoF. 2020;6(2):68. 32443916 PMC7344934 · DOI
  181. [186]Atalla MM, El-khrisy EAM, Youssef YA, Mohamed AA. Production of textile reddish brown dyes by fungi. Malays J Microbiol. 2011;7(1):33–40.
  182. [187]Chadni Z, Rahaman MH, Jerin I, Hoque KMF, Reza MA. Extraction and optimisation of red pigment production as secondary metabolites from Talaromyces verruculosus and its potential use in textile industries. Mycology. 2017;8:48–57. · DOI
  183. [188]Morales-Oyervides L, Oliveira J, Sousa-Gallagher M, Méndez-Zavala A, Montañez JC. Assessment of the dyeing properties of the pigments produced by Talaromyces spp. JoF. 2017;3:38. 29371555 PMC5715952 · DOI
  184. [189]Weber G, Chen H-L, Hinsch E, Freitas S, Robinson S. Pigments extracted from the wood-staining fungi Chlorociboria aeruginosa, Scytalidium cuboideum, and S. ganodermophthorum show potential for use as textile dyes. Color Technol. 2014;130:445–52. · DOI
  185. [190]Lagashetti AC, Dufossé L, Singh SK, Singh PN. Fungal pigments and their prospects in different industries. Microorganisms. 2019;7:604. 31766735 PMC6955906 · DOI
  186. [191]Singla S, Htut KZ, Zhu R, Davis A, Ma J, Ni QZ, et al. Isolation and characterization of allomelanin from pathogenic black knot fungus—a sustainable source of melanin. ACS Omega. 2021;6:35514–22. 34984283 PMC8717558 · DOI · Paper page
  187. [192]Jørgensen TR, Park J, Arentshorst M, van Welzen AM, Lamers G, vanKuyk PA, et al. The molecular and genetic basis of conidial pigmentation in Aspergillus niger. Fungal Genet Biol. 2011;48:544–53. 21277986 · DOI
  188. [193]Jiang H, Chi Z, Liu G-L, Hu Z, Zhao S-Z, Chi Z-M. Melanin biosynthesis in the desert-derived Aureobasidium melanogenum XJ5-1 is controlled mainly by the CWI signal pathway via a transcriptional activator Cmr1. Curr Genet. 2020;66:173–85. 31263942 · DOI
  189. [194]Yang Q, Chen Y, Ma Z. Involvement of BcVeA and BcVelB in regulating conidiation, pigmentation and virulence in Botrytis cinerea. Fungal Genet Biol. 2013;50:63–71. 23147398 · DOI
  190. [195]Schumacher J, Simon A, Cohrs KC, Traeger S, Porquier A, Dalmais B, et al. The velvet complex in the gray mold fungus Botrytis cinerea: impact of BcLAE1 on differentiation, secondary metabolism, and virulence. MPMI. 2015;28:659–74. 25625818 · DOI
  191. [196]Tsuji G, Kenmochi Y, Takano Y, Sweigard J, Farrall L, Furusawa I, et al. Novel fungal transcriptional activators, Cmr1p of Colletotrichum lagenarium and Pig1p of Magnaporthe grisea, contain Cys2His2 zinc finger and Zn(II)2Cys6 binuclear cluster DNA-binding motifs and regulate transcription of melanin biosynthesis genes in a developmentally specific manner. Mol Microbiol. 2000;38:940–54. 11123670 · DOI · Paper page
  192. [197]Bicalho Nogueira G, dos Santos LV, de Queiroz CB, Ribeiro Corrêa TL, Pedrozo Menicucci R, Soares Bazzolli DM, et al. The histidine kinase slnCl1 of Colletotrichum lindemuthianum as a pathogenicity factor against Phaseolus vulgaris L. Microbiol Res. 2019;219:110–22. 30642461 · DOI
  193. [198]Eliahu N, Igbaria A, Rose MS, Horwitz BA, Lev S. Melanin biosynthesis in the maize pathogen Cochliobolus heterostrophus depends on two mitogen-activated protein kinases, Chk1 and Mps1, and the transcription factor Cmr1. Eukaryot Cell. 2007;6:421–9. 17237364 PMC1828933 · DOI
  194. [199]Gu Q, Chen Y, Liu Y, Zhang C, Ma Z. The transmembrane protein FgSho1 regulates fungal development and pathogenicity via the MAPK module Ste50-Ste11-Ste7 in Fusarium graminearum. New Phytol. 2015;206:315–28. 25388878 · DOI
  195. [200]Wen Z, Xia Y, Jin K. MaSln1, a conserved histidine protein kinase, contributes to conidiation pattern shift independent of the MAPK Pathway in Metarhizium acridum. Microbiol Spectr. 2022;10(2): e0205121. 35343772 PMC9045129 · DOI
  196. [201]Sato K, Toriyama M. Effect of pyrroloquinoline quinone (PQQ) on melanogenic protein expression in murine B16 melanoma. J Dermatol Sci. 2009;53:140–5. 19013771 · DOI
  197. [202]Luhong K. Functional analysis of Metallophosphoesterase MaMPPED2 in Metarhizium acridum. Chongqing University. 2021. 10.27670/d.cnki.gcqdu.2021.002592. · DOI
  198. [203]Jahn B, Koch A, Schmidt A, Wanner G, Gehringer H, Bhakdi S, et al. Isolation and characterization of a pigmentless-conidium mutant of Aspergillus fumigatus with altered conidial surface and reduced virulence. Infect Immun. 1997;65:5110–7. 9393803 PMC175736 · DOI
  199. [204]Song Z, Yang J, Xin C, Xing X, Yuan Q, Yin Y, et al. A transcription factor, MrMsn2, in the dimorphic fungus Metarhizium rileyi is essential for dimorphism transition, aggravated pigmentation, conidiation and microsclerotia formation. Microb Biotechnol. 2018;11:1157–69. 30160031 PMC6196401 · DOI
  200. [205]Wang Z, Yang J, Xin C, Xing X, Yin Y, Chen L, et al. Regulation of conidiation, dimorphic transition, and microsclerotia formation by MrSwi6 transcription factor in dimorphic fungus Metarhizium rileyi. World J Microbiol Biotechnol. 2019;35:46. 30825005 · DOI

200 of 204 shown

Cited by

Sorted by citations

Authors
Qin, Y., & Xia, Y.
Affiliations
Chongqing University (CN)
Corresponding author
Xia, Yuxian
Venue
Microbial Cell Factories
Published
2024-12-19
Volume
23
Issue
1
Pages
334-334
ISSN
1475-2859 (ISSN-L)
OpenAlex
W4405528180
Cited by
57
References
3
Citations by year
2026: 31 · 2025: 26
FWCI
2.40
Type
journal article
Language
en
Open access
Locations
  • Microbial Cell Factories (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Funders
  • the Technology Innovation and Application Development Project of Chongqing (CSTB2023TIAD-KPX0045)
  • the Fundamental Research Funds for the Central Universities (2023CDJKYJH043, 2024CDJXY016)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Microbial Metabolism and Applications
  • Health Sciences › Medicine › Pharmacology › Microbial Natural Products and Biosynthesis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
Keywords
fungal melanin, melanogenesis, melanin structure, metabolic engineering, fungal secondary metabolites
MeSH terms
Fungi, Melanins, Gene Expression Regulation, Fungal, Biosynthetic Pathways, Metabolic Engineering

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review