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Associations

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Animal / dung saprobe
sporangiophore of Mucor racemosus f. sphaerosporus is saprobic in/on dung or excretions of dung of Oryctolagus cuniculus

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Ecology

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M. racemosus has a worldwide distribution and is reported frequently all over Europe, and in the Americas from Alaska to Brazil. In the tropics it is found at the higher altitudes. M. racemosus is capable of surviving various environmental conditions, thus having a large scale of habitats and hosts. Though it is mainly discovered in the soil, it has been found elsewhere such as plants residues, grains, vegetables and even in houses. 【1】Typically, it is often seen on plant-based materials such as soft fruit, fruit juice and marmalade but it has also been isolated from non-plant sources like soft camembert cheese. 【2 Recently, it has been stated in a study that M. racemosus can also be isolated from human gutmicrobiomeof non-obese individuals.【3 Another interesting thing about M. racemosus is that it is capable of biosynthesizing chitin and chitosan, which has been assumed as the reason why it can switch between the yeast-like form and mold phases. The in vivo differential rates of chitin-plus-chitosan biosynthesis in Mucor racemosus were determined under a variety of conditions, leading to yeast cell or mycelial morphology.【4Filamentous fungi grow by apical extension at the hyphal tip【5】【6. This property is believed to be the result of the fusion of vesicles containing wall synthesizing enzymes with the plasma membrane at the apex【7】【8】【9. Bartnicki- Garcia and co-workers10】【11have purified chitin synthetase-containing vesicles (chitosomes) from several diverse fungi. A few fungi are dimorphic, i.e., they are capable of growth as unicellular yeast cells or in a filamentous (mycelial) morphology. In dimorphic Mucor spp., yeast cell and mycelial walls are chemically similar12.In the yeast form, wall polymers are laid down uniformly over the entire cell surface13, leading to a spherical morphology. Presumably in yeast cells, chitosome fusion with the plasma membrane is not restricted to specific points as in the mycelial form.

References

  • 1. Abdel-Hafez, SI; Shoreit, AA (November 1985). "Mycotoxins producing fungi and mycoflora of air-dust from Taif, Saudi Arabia.". Mycopathologia. 92 (2): 65–71. PMID 3935928
  • 2. Bulliard, P. 1791. Histoire des champignons de la France. I. :1-368
  • 3. Mar Rodríguez, M; Pérez, D; Javier Chaves, F; Esteve, E; Marin-Garcia, P; Xifra, G; Vendrell, J; Jové, M; Pamplona, R; Ricart, W; Portero-Otin, M; Chacón, MR; Fernández Real, JM (12 October 2015). "Obesity changes the human gut mycobiome.". Scientific Reports. 5: 14600. PMID 26455903.
  • 4. Domek, DB; Borgia, PT (June 1981). "Changes in the rate of chitin-plus-chitosan synthesis accompany morphogenesis of Mucor racemosus.". Journal of bacteriology. 146 (3): 945–51. PMID 7240089.
  • 5. Bartnicki-Garica,S., and E. Lippman. 1969.Fungal morphogenesis: cell wall construction in Mucor rouxii. Science165:302-304.
  • 6. Hunsley,D.,andD.Kay.1976.Wall structure of Neu- rospora hyphal apex: immunofluorescent localization of wall surface antigens. J. Gen. Microbiol. 95:233-248.
  • 7. Bartnicki-Garcia, S. 1973. Fundamental aspects of hyphal morphogenesis. Symp.Soc.Gen.Microbiol.23:245-267.
  • 8. Farkas, V. 1979. Biosynthesis of cell walls of fungi. Microbiol. Rev.43:117-144.
  • 9. Gooday G. W., and A.J.P. Trinci 1980. Wall structure and biosynthesis in fungi. Symp. Soc. Gen. Microbiol. 30:207-251.
  • 10. Bartnicki-Garcia, S., C.E. Bracker, E. Reyes, and J. Ruiz-Herrera. 1978. Isolation of chitosomes from taxonomically diverse fungi and synthesis of microfibrils in vitro. Exp. Mycol. 2:173-192.
  • 11. Bracker, C.E., J. Ruiz-Herrera, and S. Bartnicki-Garcia. 1976. Structure and transformation of chitin 
synthetase particles (chitosomes) during microfibril synthesis in vitro. Proc. Natl. Acad. Sci. U.S.A. 73: 4570-4575.
  • 12. Bartnicki-Garcia, S. 1968. Cell wall chemistry, morphogenesis and taxonomy of fungi. Annu. Rev. Microbiol. 22:103-117.
  • 13. Bartnicki-Garica, S., and E.Lippman.1969.Fungal morphogenesis: cell wall construction in Mucor rouxii. Science165:302-304


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Morphology

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M. racemosus has hyphae without septa and is multi-core and branched-like. It can spread both inside and outside of the substrate. It does not possess rhizoid or stolon and does not produce shaped colonies. Sporangiophores directly germinate from hymenium in the form of monopodial, racemose or false diachotomous branching. There are different shapes of columella inside of sporangia that are located on the tips of each branch. The sporangia produce a large number of sporangiospores that are smooth and have thin walls. Sporangia will release the spores once they become mature. Sexual reproduction can be heterothallic or homothallic. M. racemosus is a dimorph fungi, possessing the ability to form both filamentous and yeast-like morphologies.【1】 The differences between these two forms are significant and the environment conditions have huge impact on the phases of M. racemosus. When given anaerobic conditions, it may exhibit yeast-like morphology. Anaerobic conditions and 30% carbon dioxide presence stimulate conversion to yeast form. It has also been reported that adding Tween 80,ergosterol when culturing M. racemosus and supplied with 100% nitrogenalso helps it convert to yeast-like form.【2】Conversely, increasing oxygen concentration may lead to the yeast-like form to the mold form.【3】 In the laboratory, the fungus forms dark grey or light grey colonies on most common laboratory media.【4】 Like many other fungi, M. racemosus can produce both sexual and asexual spores depending on environmental conditions. 【3】During sexual reproduction, hyphae of compatible mating types touch and fuse, ultimately giving rise to a thick-walled zygosporangium containing a single zygospore. Germination from the zygospore leads to growth of new hyphae that give rise to asexual spores of both + and - mating type.Germination of these spores produces new haploid hyphae of the same mating type. 【3】 It is easily recognizable microscopically by its tall (up to 2 cm) needle-like sporangiophores and large sporangium.

References

  • 1. Mendez-Vilas, edited by A. (2010). Current research, technology and education topics in applied microbiology and microbial biotechnology. Badajoz, Spain: Formatex Research Center. pp. 201–212. ISBN 978-84-614-6194-3.
  • 2. Lübbehüsen, TL; Nielsen, J; McIntyre, M (February 2003). "Morphology and physiology of the dimorphic fungus Mucor circinelloides (syn. M. racemosus) during anaerobic growth.". Mycological research. 107 (Pt 2): 223–30. PMID 12747334
  • 3. Bekada, A.M.A.; Benakriche, B.; Hamadi, K.; Bensoltane, A. (2008). "Modelling of Effects of Water Activity, pH and Temperature on the Growth Rate of Mucor racemosus Isolated from Soft Camembert Cheese" (PDF). World Journal of Agricultural Sciences. Laboratory of Food and Industrial Microbiology Department of Biology, Faculty of Sciences, University of Oran, Algeria: IDOSI Publications. 4 (6). ISSN 1817-3047. Retrieved 3 February 2014.
  • 4. Bulliard, P. 1791. Histoire des champignons de la France. I. :1-368

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Relationships with Human Beings

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·Human pathogen

Mucoris an uncommon opportunistic pathogen. Usually it will not attack human beings, but sometimes it will attack individuals with significantly compromised immune systems such as children, elderly and diseased patients like those with HIV. M. racemosushas also been associated with causation of extrinsic allergic alveolitis 1. The symptoms, which may occur 6 to 8 hours after exposure, include: elevated temperature, flu-like symptoms, general malaise, and difficulty in breathing followed by asthma later.

·Commercial use

M. racemosus can grow as a yeast, thus it has the ability to form biochemicals which can be used in industry and our daily lives. For instance, it can produce a high yield ofphytase, an important industrial enzyme. Phytase may be produced efficiently by M. racemosus in solid-state fermentation on optimized coconut oil cake at 71% moisture level, pH 5.5, incubation temperature 25 °C. By optimized nutrient supplementation and selecting the most appropriate carbon and nitrogen sources production nearly doubled (from 14.5 IU/g DM to 26 IU/g DM). The quality of carbon and nitrogen sources appears to be critical factors for maximal phytase production【2.

References

  • 1. Koschel D, Sennekamp J, Schurz C, Muller-Wening D. Misting-fountain-alveolitis. [German] Pneumologie 2004:58(9):666-9.
  • 2. Bogar, B.; Szakacs, G.; Pandey, A.; Abdulhameed, S.; Linden, J.C.; Tengerdy, R.P. (4 April 2003). "Production of Phytase by Mucor racemosus in Solid-State Fermentation". Biotechnology Progress. 19 (2): 312–319. doi:10.1021/bp020126v.

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Taxonomy and Phylogeny

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Mucor includes at least 39 species, belonging to phylum zygomycota, order Mucorales, Mucoraceae family. M. racemosus was first described and named by Bulliard in 1791.1 It is one of the earliest species people discovered in soil and was isolated long time ago——as early as 1886.2M. racemosus has several synonyms such as Calyptromyces globosus, Circinomucor sphaerosporus, M.dimorphosporus f. sphaerosporus, M. globosus, M. macrosporus, M. sphaerosporus and so on. This species is closely related to M. mucedo and M.rouxianus, since they all belong to the same genus and share lots of similar characters.

References

  • 1. Bulliard, P. 1791. Histoire des champignons de la France. I. :1-368
  • 2. Bekada, A.M.A.; Benakriche, B.; Hamadi, K.; Bensoltane, A. (2008). "Modelling of Effects of Water Activity, pH and Temperature on the Growth Rate of Mucor racemosus Isolated from Soft Camembert Cheese" (PDF). World Journal of Agricultural Sciences. Laboratory of Food and Industrial Microbiology Department of Biology, Faculty of Sciences, University of Oran, Algeria: IDOSI Publications. 4 (6). ISSN 1817-3047. Retrieved 3 February 2014.

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Mucor racemosus

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Mucor racemosus is a rapidly growing, weedy mould belonging to the division Mucoromycota.[1] It is one of the earliest fungi to be grown in pure culture and was first isolated in 1886. It has a worldwide distribution and colonizes many habitats such as vegetational products, soil and houses.[2][3] The fungus is mostly known for its ability to exhibit both filamentous and yeast-like morphologies, often referred to as dimorphism.[2] Stark differences are seen in both forms and conditions of the environment heavily affect the phases of the M. racemosus.[2] Like many fungi, it also reproduces both sexually and asexually.[2] The dimorphic capacity of this species has been proposed as an important factor in its pathogenicity and has enhanced the industrial importance. This species is considered an opportunistic pathogen, generally limited to immunocompromised individuals.[4] It also been associated with allergy and inflammations of facial sinuses.[4] Its association with allergy has made it a common fungus used in allergen medical testing.[5][6] Industrial use of the fungus is in the production of enzymes and the manufacture of certain dairy foods.[7][8][9]

Morphology and taxonomy

The dimorphic form of the species mainly exists and grows vegetatively as either a filamentous hyphae (mould form) or as spherical yeast (yeast form).[2] However, the organism is best known from the mould form which is characterised by the production of asexual reproductive state consisting of tall (up to 2 cm) needle-like sporangiophores with an apical swelling enclosed by a large sporangium filled with ellipsoidal, single-celled, smooth-walled, unpigmented sporangiospores. In the laboratory, the fungus forms dark grey or light grey colonies on most common laboratory media. If subjected to anaerobic conditions, the fungus may convert to the yeast-like form.[2] Anaerobic conditions and 30% carbon dioxide presence stimulate conversion to yeast form. Likewise, cultures supplemented with Tween 80, ergosterol and supplied with 100% nitrogen also converted to yeast.[10] Conversely, increasing oxygen concentration will cause conversion of the yeast form to the mould form.[2] Like many zygomycetes, M. racemosus reproduces both sexually and asexually depending on environmental conditions. During sexual reproduction, hyphae of compatible mating types touch and fuse, ultimately giving rise to a thick-walled zygosporangium containing a single zygospore. Germination from the zygospore leads to growth of new hyphae that give rise to asexual spores of both + and - mating type.[2] Germination of these spores produces new haploid hyphae of the same mating type.[2]

Physiology and ecology

Mucor racemosus (UAMH 8346) cultured on potato dextrose agar at 25 °C for 10 days.

M. racemosus possesses the ability to exhibit multiple morphology (mainly, filamentous and spherical shape) to withstand various environmental stress.[11] This has given it ability to survive many conditions and it has a worldwide distribution, reported most frequently in Europe as well as Americas. In the tropics, it has been seen at higher altitudes. While the species is primarily soil-based, it has been shown to exist elsewhere such as in horse manure, plant remains, grains, vegetables and nuts.[2] Typically, it is often seen on plant-based materials such as soft fruit, fruit juice and marmalade but it has also been isolated from non-plant sources like soft camembert cheese. M. racemosus has also been isolated from the human gut microbiome of non-obese individuals.[12] It is the most common mould found in the floor dust in houses and is largely considered as an indoor mould.[3]M. racemosus is uniquely known for its ability to display multiple morphologies but most of the time, studies are made based on the dimorphic form of the species.[11] It is a facultative anaerobic zygomycote and fast-growing, conferring it ability to survive in multiple conditions/locations all over the world.[2][11] M. racemosus possesses the ability to biosynthesize chitin and chitosan, which has been proposed as a mechanism supporting the ability of the fungus to switch between the yeast and the mould phases.[13] Genomic analysis of M. racemosus has revealed genes similar to human RAS genes, and it is proposed that these genes help with germination and dimorphism.[14][15] Protein kinase A (PKA) genes such as pkaR are highly also expressed during dimorphic shift.[16]

Human disease

M. racemosus is a rare agent of human disease, typically only associated with opportunistic infection of immunocompromised individuals such as children, elderly and diseased patients (HIV, Ebola etc.).[11] It is an agent of Mucormycosis, a potentially life-threatening infection often involving the head airways.[4] Pulmonary, cutaneous, and gastrointestinal (GI) infections have also been observed leading to an array of clinical presentations in infected individuals. Risk factors such as diabetic ketoacidosis and neutropenia are present in most cases.[4] Treatment of M. racemosus can be difficult due to histopathologic differentiation of the fungus.[1] In addition to commonly used antifungal agents, biological compounds like Lovastatin, Aleuria aurantia lectin (AAL) and antimicrobial peptides (AMPs LR14) have been isolated and showed antimicrobial effects towards M. racemosus.[17][18][19] Allergies to M. racemosus have been reported to affect immunologically normal individuals from in a range of places (Netherlands, Turkey and Brazil).[20][21][22] Allergy to M. racemosus has been also associated with fungal rhinosinusitis,[23] rhinitis and extrinsic allergic alveolitis.[24][25] Asthmatic patients have also shown elevated sensitization to M. racemosus.[26] Mucor racemosus-specific IgE antibody is commonly used and available for medical as well as laboratory use in allergen assay (ImmunoCAP).[5][6]

Commercial and biotechnological use

The capacity of M. racemosus to grow as a yeast and its various abilities to manufacture biochemicals have led to its use in industry. For example, it can produce a high yield of phytase, an important industrial enzyme.[7][8] It also has an increased extracellular protease activity, suggesting its biotechnological suitability for the production of other industrial enzymes.[7][8] It is also used in production of homeopathic medicinal products.[27] In the manufacture of sufu (fermented cheese-like soybean product common in China and Vietnam), the fungal fermentation of soybean curd (tofu) results in moulded tofu, pehtze. The final product (sufu) is obtained by maturing pehtze in a brine containing alcohol and salt for several months.[9]

It possesses the ability to adapt phenotypically to several different antibiotics after exposure to a single drug, which makes it a good model for phenotypic multidrug resistance in lower eukaryotes. It has been shown to adapt to famous antibiotics like cycloheximide, trichodermin and amphotericin B.[2][28] Cells adapted to cycloheximide particularly have been observed to be 40-times more resistant than non-adapted cells to the drug. These adapted cells have been studied to better understand their greater efficiency of membrane transport (efflux of drugs).[29]

Mucor racemosus can biotransform lipids like 4-ene-3-one steroids and 20(S)-Protopanaxatriol into several different products, some of which have anticancer properties (as the metabolites resulted in increased intracellular calcium ion content, leading to cell cycle arrest and apoptosis).[30][31] Two of the products formed from this biotransformation are two novel hydroperoxylated metabolites that have been shown to be effective against prostate cancer cells.[32] Secondary metabolites of M. racemosus do not exhibit genotoxic activity, and the species is not known to be a producer of mycotoxins. However, some secondary metabolites of the fungus have been found to have anti-inflammatory activity similar to the drug dexamethasone .[33]

References

  1. ^ a b Hata, DJ; Buckwalter, SP; Pritt, BS; Roberts, GD; Wengenack, NL (July 2008). "Real-time PCR method for detection of zygomycetes". Journal of Clinical Microbiology. 46 (7): 2353–8. doi:10.1128/jcm.02331-07. PMC 2446880. PMID 18480229.
  2. ^ a b c d e f g h i j k l Mendez-Vilas, A., ed. (2010). Current research, technology and education topics in applied microbiology and microbial biotechnology. Badajoz, Spain: Formatex Research Center. pp. 201–212. ISBN 978-84-614-6194-3.
  3. ^ a b Abdel-Hafez, SI; Shoreit, AA (November 1985). "Mycotoxins producing fungi and mycoflora of air-dust from Taif, Saudi Arabia". Mycopathologia. 92 (2): 65–71. doi:10.1007/bf00444085. PMID 3935928. S2CID 2285355.
  4. ^ a b c d Nancy, Crum-Cianflone (4 October 2018). "Mucormycosis". Medscape. WebMD.
  5. ^ a b "Mucor Racemosus IgE". Viracor.IBT Laboratories.
  6. ^ a b "Allergen, Fungi and Molds, Mucor racemosus". Arup Laboratories.
  7. ^ a b c Bogar, B.; Szakacs, G.; Pandey, A.; Abdulhameed, S.; Linden, J.C.; Tengerdy, R.P. (4 April 2003). "Production of Phytase by Mucor racemosus in Solid-State Fermentation". Biotechnology Progress. 19 (2): 312–319. doi:10.1021/bp020126v. PMID 12675565. S2CID 27701060.
  8. ^ a b c Alves, MH; de Campos-Takaki, GM; Okada, K; Ferreira-Pessoa, IH; Milanez, AI (June 2005). "[Detection of extracellular protease in Mucor species]". Revista Iberoamericana de Micologia. 22 (2): 114–7. doi:10.1016/s1130-1406(05)70020-6. PMID 16107171.
  9. ^ a b Han, BZ; Kuijpers, AF; Thanh, NV; Nout, MJ (April 2004). "Mucoraceous moulds involved in the commercial fermentation of Sufu Pehtze". Antonie van Leeuwenhoek. 85 (3): 253–7. doi:10.1023/b:anto.0000020157.72415.b9. PMID 15028872. S2CID 2214535.
  10. ^ Lübbehüsen, TL; Nielsen, J; McIntyre, M (February 2003). "Morphology and physiology of the dimorphic fungus Mucor circinelloides (syn. M. racemosus) during anaerobic growth" (PDF). Mycological Research. 107 (Pt 2): 223–30. doi:10.1017/s0953756203007299. PMID 12747334. S2CID 12643028. Archived from the original (PDF) on 8 February 2020.
  11. ^ a b c d Inderlied, Clark; Peters, Julius; Cihlar, Ronald (1985). Fungal Dimorphism With Emphasis on Fungi Pathogenic for Humans. Boston, MA: Springer US. pp. 337–359. ISBN 978-1-4684-4982-2.
  12. ^ Mar Rodríguez, M; Pérez, D; Javier Chaves, F; Esteve, E; Marin-Garcia, P; Xifra, G; Vendrell, J; Jové, M; Pamplona, R; Ricart, W; Portero-Otin, M; Chacón, MR; Fernández Real, JM (12 October 2015). "Obesity changes the human gut mycobiome". Scientific Reports. 5: 14600. doi:10.1038/srep14600. PMC 4600977. PMID 26455903.
  13. ^ Domek, DB; Borgia, PT (June 1981). "Changes in the rate of chitin-plus-chitosan synthesis accompany morphogenesis of Mucor racemosus". Journal of Bacteriology. 146 (3): 945–51. doi:10.1128/jb.146.3.945-951.1981. PMC 216948. PMID 7240089.
  14. ^ Casale, WL; Mcconnell, DG; Wang, SY; Lee, YJ; Linz, JE (December 1990). "Expression of a gene family in the dimorphic fungus Mucor racemosus which exhibits striking similarity to human ras genes". Molecular and Cellular Biology. 10 (12): 6654–63. doi:10.1128/mcb.10.12.6654. PMC 362943. PMID 1701021.
  15. ^ Roze, LV; Mahanti, N; Mehigh, R; McConnell, DG; Linz, JE (December 1999). "Evidence that MRas1 and MRas3 proteins are associated with distinct cellular functions during growth and morphogenesis in the fungus Mucor racemosus". Fungal Genetics and Biology. 28 (3): 171–89. doi:10.1006/fgbi.1999.1177. PMID 10669583. S2CID 10097338.
  16. ^ Wolff, AM; Appel, KF; Petersen, JB; Poulsen, U; Arnau, J (May 2002). "Identification and analysis of genes involved in the control of dimorphism in Mucor circinelloides (syn. racemosus)". FEMS Yeast Research. 2 (2): 203–13. doi:10.1016/s1567-1356(02)00090-9. PMID 12702308.
  17. ^ Amano, K; Katayama, H; Saito, A; Ando, A; Nagata, Y (2012). "Aleuria aurantia lectin exhibits antifungal activity against Mucor racemosus". Bioscience, Biotechnology, and Biochemistry. 76 (5): 967–70. doi:10.1271/bbb.110982. PMID 22738968.
  18. ^ Gupta, R; Srivastava, S (September 2014). "Antifungal effect of antimicrobial peptides (AMPs LR14) derived from Lactobacillus plantarum strain LR/14 and their applications in prevention of grain spoilage". Food Microbiology. 42: 1–7. doi:10.1016/j.fm.2014.02.005. PMID 24929709.
  19. ^ Roze, LV; Linz, JE (November 1998). "Lovastatin triggers an apoptosis-like cell death process in the fungus Mucor racemosus". Fungal Genetics and Biology. 25 (2): 119–33. doi:10.1006/fgbi.1998.1093. PMID 9974223. S2CID 20675105.
  20. ^ Beaumont, F; Kauffman, HF; de Monchy, JG; Sluiter, HJ; de Vries, K (April 1985). "Volumetric aerobiological survey of conidial fungi in the North-East Netherlands. II. Comparison of aerobiological data and skin tests with mould extracts in an asthmatic population". Allergy. 40 (3): 181–6. doi:10.1111/j.1398-9995.1985.tb00214.x. PMID 4039540. S2CID 33305473.
  21. ^ Güneser, S; Atici, A; Köksal, F; Yaman, A (1994). "Mold allergy in Adana, Turkey". Allergologia et Immunopathologia. 22 (2): 52–4. PMID 8059675.
  22. ^ Mohovic, J; Gambale, W; Croce, J (1998). "Cutaneous positivity in patients with respiratory allergies to 42 allergenic extracts of airborne fungi isolated in São Paulo, Brazil". Allergologia et Immunopathologia. 16 (6): 397–402. PMID 3242377.
  23. ^ Zhao, Z; Li, L; Wan, Z; Chen, W; Liu, H; Li, R (April 2011). "Simultaneous detection and identification of Aspergillus and mucorales species in tissues collected from patients with fungal rhinosinusitis". Journal of Clinical Microbiology. 49 (4): 1501–7. doi:10.1128/jcm.02262-10. PMC 3122857. PMID 21325541.
  24. ^ Koschel, D; Sennekamp, J; Schurz, C; Müller-Wening, D (September 2004). "[Misting-fountain-alveolitis]". Pneumologie (Stuttgart, Germany). 58 (9): 666–9. doi:10.1055/s-2004-830044. PMID 15343489.
  25. ^ Namysłowski, G; Rogala, B; Mrówka-Kata, K; Ponińska-Polańczuk, J (1998). "[The role of imperfect fungi in etiopathogenesis of allergic rhinitis]". Otolaryngologia Polska. The Polish Otolaryngology. 52 (3): 277–80. PMID 9760768.
  26. ^ Soeria-Atmadja, D; Onell, A; Kober, A; Matsson, P; Gustafsson, MG; Hammerling, U (December 2007). "Multivariate statistical analysis of large-scale IgE antibody measurements reveals allergen extract relationships in sensitized individuals". The Journal of Allergy and Clinical Immunology. 120 (6): 1433–40. doi:10.1016/j.jaci.2007.07.021. PMID 17825892.
  27. ^ Wiethoff, K; Bader, G (21 August 2013). "Characterization and specification finding of Mucor racemosus preparation used as homeopathic starting material". Planta Medica. 79 (13). doi:10.1055/s-0033-1352302.
  28. ^ Leathers, TD; Sypherd, PS (June 1985). "Inducible phenotypic multidrug resistance in the fungus Mucor racemosus". Antimicrobial Agents and Chemotherapy. 27 (6): 892–6. doi:10.1128/aac.27.6.892. PMC 180181. PMID 4026262.
  29. ^ Shearer G, Jr; Sypherd, PS (March 1988). "Cycloheximide efflux in antibiotic-adapted cells of the fungus Mucor racemosus". Antimicrobial Agents and Chemotherapy. 32 (3): 341–5. doi:10.1128/aac.32.3.341. PMC 172172. PMID 3364951.
  30. ^ Ge, WZ; Li, N; Shan, LH; Liu, HM (June 2007). "[Microbial transformation of 4-ene-3-one steroids by Mucor racemosus]". Wei Sheng Wu Xue Bao = Acta Microbiologica Sinica. 47 (3): 540–3. PMID 17672323.
  31. ^ Chen, G; Yang, X; Nong, S; Yang, M; Xu, B; Zhang, W (March 2013). "Two novel hydroperoxylated products of 20(S)-protopanaxadiol produced by Mucor racemosus and their cytotoxic activities against human prostate cancer cells". Biotechnology Letters. 35 (3): 439–43. doi:10.1007/s10529-012-1098-x. PMID 23183919. S2CID 1246825.
  32. ^ Chen, G; Ge, H; Song, Y; Li, J; Zhai, X; Wu, J; Ling, X (October 2015). "Biotransformation of 20(S)-protopanaxatriol by Mucor racemosus and the anti-cancer activities of some products". Biotechnology Letters. 37 (10): 2005–9. doi:10.1007/s10529-015-1877-2. PMID 26054722. S2CID 15170557.
  33. ^ Meier, SM; Muqaku, B; Ullmann, R; Bileck, A; Kreutz, D; Mader, JC; Knasmüller, S; Gerner, C (2015). "Proteomic and Metabolomic Analyses Reveal Contrasting Anti-Inflammatory Effects of an Extract of Mucor Racemosus Secondary Metabolites Compared to Dexamethasone". PLOS ONE. 10 (10): e0140367. doi:10.1371/journal.pone.0140367. PMC 4619718. PMID 26496078.
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Mucor racemosus: Brief Summary

provided by wikipedia EN

Mucor racemosus is a rapidly growing, weedy mould belonging to the division Mucoromycota. It is one of the earliest fungi to be grown in pure culture and was first isolated in 1886. It has a worldwide distribution and colonizes many habitats such as vegetational products, soil and houses. The fungus is mostly known for its ability to exhibit both filamentous and yeast-like morphologies, often referred to as dimorphism. Stark differences are seen in both forms and conditions of the environment heavily affect the phases of the M. racemosus. Like many fungi, it also reproduces both sexually and asexually. The dimorphic capacity of this species has been proposed as an important factor in its pathogenicity and has enhanced the industrial importance. This species is considered an opportunistic pathogen, generally limited to immunocompromised individuals. It also been associated with allergy and inflammations of facial sinuses. Its association with allergy has made it a common fungus used in allergen medical testing. Industrial use of the fungus is in the production of enzymes and the manufacture of certain dairy foods.

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