Ergothioneine: The Elusive Amino Acid

 

Proving that mushrooms are an essential part of the human diet 

 

 

Definitions to consider while reading:

Antioxidant­: Compounds that mitigate oxidation. Oxidation is a reaction that can produce free radicals, leading to cellular damage. Antioxidants such as thiols and ascorbic acid (vitamin C) terminate these reactions by donating electrons. To balance oxidative states, living organisms maintain systems with overlapping antioxidants such as glutathione, catalase, superoxide dismutase.

 Blood-brain barrier: a filtering mechanism of the capillaries that carry blood to the brain and spinal cord tissue, blocking the passage of certain substances.

Cation chelator: a type of bonding of ions and molecules to metal ions. There is application of this in removing toxic metals from the body. 

Glutathione: Glutathione is a tripeptide (cysteine, glycine, and glutamic acid) found in surprisingly high levels—5 millimolar—concentrations in most cells. Responsible for the following actions in the body: (Pizzorno)

  1. Direct chemical neutralization of singlet oxygen, hydroxyl radicals, and superoxide radicals
  2. Cofactor for several antioxidant enzymes
  3. Regeneration of vitamins C and E
  4. Neutralization of free radicals produced by Phase I liver metabolism of chemical toxins
  5. One of approximately 7 liver Phase II reactions, which conjugate the activated intermediates produced by Phase I to make them water soluble for excretion by the kidneys
  6. Transportation of mercury out of cells and the brain
  7. Regulation of cellular proliferation and apoptosis
  8. Vital to mitochondrial function and maintenance of mitochondrial DNA (mtDNA)

Lipid peroxidation: The oxidative degradation of lipids. It is the process in which free radicals “steal” electrons from the lipids in cell membranes, resulting in cell damage. (Wik)

Oxidative stress: disturbance in the balance between the production of reactive oxygen species (free radicals) and antioxidant defenses (Betteridge)

IMG_4412
Pleurotus ostreatus – Oyster Mushroom

 

‘Constituentism’

I am not necessarily a fan of isolation and ‘constituentism’ in supplemental medicine – especially when a constituent has been isolated from its synergistic community of molecules from the whole plant or whole mushroom and is considered supposedly different than a pharmaceutical. Though, I do love to understand the individual constituents in organisms and how they work independently, in order to better understand how they work synergistically. There is also a greater understanding to be had of how animals, plants, fungi and bacteria all evolved together when we can explore specific plant and fungi constituent mechanisms with specific cellular receptors and transporters in the animal organism. A specific example of this is a compound called Ergothioneine (ERG). ERG is an amino acid derivative, specifically a crystalline betaine, derivative of histidine – the etymology explains; ergot- (found in ergot (fungus) thione- (double bond to a Sulphur) and  -ine (amine containing)—basically a sulphur containing amine found in fungi. ERG is also found in Actinobacteria (gram positive bacteria that behave similar to fungi in soil, helping to decompose the organic matter of dead organisms so the molecules can be taken up by new plants, they even grow extensive mycelium like fungi and were in fact long believed to be fungi) and Cyanobacteria, commonly known as blue-green algea, (another abnormal bacteria that can actually obtain their energy from photosynthesis – they are the only photosynthetic prokaryote able to produce oxygen). (blankenfeldt)

 

Specific ERG transporters in the animal

We have evolved so closely with mushrooms that we have specific transporters and receptors uniquely for mushroom compounds. ERG is no exception.  While we have a specific receptor for ERG, we cannot synthesize this molecule ourselves, and as I will describe later, we are discovering this compound is extremely important for human health.  The ERG transporter, OCTN1, (gene: SLC22A4) is found specifically on erythrocytes, fetal liver and bone marrow, ileum of the small intestine, trachea, kidney, cerebellum, lung, monocytes, seminal vesicles and the lens and cornea of the eye (Halliwell). Interestingly, ERG transporter is concentrated in the mitochondria of cells – suggesting a role in protecting mitochondrial components from DNA damage (Paul, Halliwell). This transporter’s only known role is to sequester as much ERG within the cells as is available, and only cells with this transporter can absorb, distribute, and retain this compound (Grundermann). Researchers explored the effects when cells were depleted of this transporter, the results being that cells were more susceptible to oxidative stress, leading to mitochondrial damage, protein oxidation, and lipid peroxidation. Once taken up into the cell, ERG is extremely bioavailable and is retained for up to a month within the body.

 IMG_4117

Bioavailability of ergothioneine from mushroom consumption

Once consumed in the diet, whether it be the isolated molecule or from whole mushrooms, ERG is quickly absorbed into the blood stream. Human erythrocytes (red blood cells, RBC) contain 2-9 fold more ERG than plasma. Interestingly, concentration is lowest in early life (1-10yo), increases between 11-18yo and reaches maximum value of 3.7mg/100mL by age 18. In this study, subjects consumed 8g and 16g of mushrooms and increases in red blood cell ERG were observed. After 1 and 4hr of consumption, the 16g mushroom dose increased RBC ERG concentration compared to the control, and after only 2 hrs of 16g of mushroom consumption, RBC ERG concentration was significantly higher than the control. Variability in bioavailablity was due to genetic variations in the SLC22A4 gene (Heller, Kris-etherton, Beelman). Interestingly, mutations in the ERG transporter have been identified as a susceptibility factor for autoimmune disorders, such as rheumatoid arthritis and Crohn’s disease, as well as neurodegenerative disorders, such as dementia and Parkinson’s (Paul, Snyder). 

IMG_0914

Why do we care – Once ergothioneine is in the cell, then what happens?

Ergothioneine as an antioxidant and cytoprotectant: The distribution of ERG transporters may seem random, but on closer inspection, they seem to be present in tissues predisposed to high levels of oxidative stress and inflammation (Halliwell). In animal studies, animals who were completely deficient in ERG had higher levels of reactive oxygen species and were therefore more susceptible to oxidative stress. In vitro, ERG is a powerful scavenger of hydroxyl radical and has been shown to deactivate singlet oxygen at a higher rate than glutathione (Hseu, Servillo). Similar results were proven in vivo – rats supplemented with ERG had lower levels of lipid peroxidation and higher levels of glutathione and alpha-tocopherol. As one might surmise, ERG and glutathione seem to have an intimate relationship within the cell. Glutathione is considered the major intracellular antioxidant in almost all organisms and has important functions in detoxification and immune function. It has been proposed, based on current research, that ERG can help maintain GSH levels in the presence of oxidative burden by interacting with other cellular defense systems. The maintenance of glutathione tissue levels is important in maintaining health as depletion will impair immune function. Conveniently, mushrooms contain both glutathione and ERG. In fact, mushrooms have been observed to have higher GSH amounts than any vegetable or fruit. Grifola frondosa (Maitake), Hericium erinaceus (Lions mane), Pleurotus ostreatus (Oyster mushroom), Boletus edulis (porcini) and Lentinus edodes (shitake) containing the most, respectively (Kalaras). Considering the relationship between ERG and GSH in mushrooms, a correlation analysis found that mushrooms high in GSH were also high in ERG, specifically the caps or pileus of the mushrooms (kalaras). All this said, mushrooms are an important source for cellular antioxidants.

Cation chelator: ERG chelates divalent metal cations – specifically, Cu2, hg, Zn, Cd, Co, Fe, and Ni (Cheah, Song, Kerley). Binding these cations in the body may help prevent their participation in the generation of reactive oxygen species. For example, EGT has been found to protect DNA and protein against copper induced oxidative damage through formation of a redox-inactive EGT-Cu complex. Interestingly, the high levels of ERG in semen – due to the high concentration of ERG OCTN1 transporter on the seminal vesicles- have been shown to prevent Cu inhibition of sperm motility. There is more to be explored between the relationship of ERG and semen viability.

Ergothioneine, aging, and cognitive decline: As we age, we are more vulnerable to the oxidative stress and environmental toxins that slowly damage our DNA, making us more susceptible to neurodegeneration – one of many conditions associated with DNA damage from oxidative stress. Low levels of glutathione have been linked to certain neurodegenerative diseases including Parkinson’s disease (Wei, Shah). ERG was able to dose dependently enhance glutathione activity in the rat liver cytosol—leading researchers to postulate that declining ERG may play a role in age related decline of GSH and glutathione peroxidase. Furthermore, ERG levels were found to be lower in the elderly with early stages of dementia and in PD patients relative to age matched healthy controls (Cheah). In animal studies, oral administration of ERG protected neurons and preserved cognitive function following administration of toxic amyloid beta cisplatin or D-galactose. It is now understood that the presence of Octn1 transporter in the blood brain barrier is responsible for these neuroprotective actions. Captivatingly, researchers found that there is a direct relationship between whole blood and brain ERG levels following consumption (Cheah). It is rare for compounds to be bioavailable in this way and transported across the blood brain barrier so readily – even glutathione needs to be taken intranasal for treatment of neurodegeneration.

Ergothioneine human trial: uptake metabolism and effects

While there is undeniably a lack of human trials exploring the in vivo effects of ERG, a recent study from 2017 explored ERG uptake, metabolism, and effects on biomarkers of oxidative damage and inflammation in healthy human subjects (cheah, Tang). One of the most interesting aspects of ERG discussed in this particular article is that ERG is a tautomer. This means that it exists in two forms – thione and thiol. The thiol is a single bond to sulfur and the thione is a double bond to sulfur. The article explains that in animal physiologic conditions, ERG primarily exists as the thione tautomer – under circumstances of low stress in the body, ERG remains in its thione tautomer form and is not the first choice as an antioxidant, rather endogenous antioxidants like glutathione are preferred (glutathione is a primary antioxidant thiol in the body). When the cells undergo higher levels of oxidative stress, ERG transforms into its thiol tautomer form and is then used for extra support. Additionally, under levels of elevated stress, tissues have increased amounts of the ERG, supposedly by upregulating expression of the OCTN1 ERG transporter in response to inflammatory cytokines.

This study also found that ERG can be stored in the cells for up to a month. It is theorized that ERG is stored for an extended period of time following consumption until it is required as a stronger defense mechanism.

During administration of ERG, plasma levels significantly elevated, while whole blood levels steadily increased for up to four weeks after administration stopped (red blood cells could continue to take ERG up as needed), and the excretion of ERG in the urine remained low, indicating that ERG is absorbed and retained in the body after oral administration. While this study used pure ERG, other studies previously mentioned (Heller) prove this same high bioavailability of ERG from dietary mushrooms, and so I will consider this as true for dietary ERG.

IMG_1993

Mushroom analyses of ergothioneine: Fruiting body or mycelium? Gilled mushrooms or polypore mushrooms?

ERG was highest in the fruiting body of Pleurotus ostreatus and in the mycelium of Pleurotus eryngii. Generally, fruiting bodies and mycelium contained different amounts of ERG, with Pleurotus genus containing the highest amounts overall (Chen). Among simple mushrooms, fruiting body of White Button had the least (1.4mg erg per 85g mushroom) and Portabella the highest (2.7mg erg per 85g mushroom). While among specialty mushrooms, Maitake had the least (16.3mg erg per 85g mushroom) and oyster the highest (26.4mg per 85g mushroom) (Dubost).

Fruiting bodies of gilled mushrooms, specifically the cap, contain the most ERG, while polypore mushrooms contain very small amounts. Interestingly, the mycelium of Ganoderma contains more ERG than the fruiting body, but still not as much as the fruiting bodies of Shitake, Matsutake, Oyster, and Maitake (Lee, Wang).

Extraction:

Hot water extraction is sufficient to extract ERG from mushrooms.

In a study that explored water extraction – temperature of water, ratio of water to mycelium and the extraction rate of ERG, the following information was found:

Most notable: at 85°C and 20:1 ratio of mycelium to water, the extraction rate of ERG was 91.2% – the least effective yield of ERG was at 78°C and a 20:1 ratio of mycelium to water. There was no difference in ERG concentration between 5 minutes and 120 minutes, so a long boil to extract EGR is not necessary (Zhang).

In Summary:

Ergothioneine is a water soluble compound that is most abundant in Oyster mushrooms. There are transporters on different tissues in the body that are highly specific to ergothioneine. Ergothioneine is readily absorbed into the blood after consumption of mushrooms and stored in tissues for up to 1 month. In times of excessive oxidative stress, ergothioneine is taken up by those tissues and used as an antioxidant. Of note: there are transporters on the blood brain barrier and there is an association with low ergothioneine and age-related cognitive decline. In a world full of environmental toxins that are mostly impossible to escape, we might as well eat more mushrooms and get some extra protection.

How to apply this information to your life:

Eat a lot of mushrooms, especially Oyster mushrooms.

Oyster Mushroom Recipes

Resources for ergothioneine rich mushrooms around the Seattle area:

Cascadia Mushrooms

Sno-Valley Mushrooms

Work Cited

Antonicelli F, Aruoma OI. Ergothioneine inhibits oxidative stress- and TNF- a -induced NF- j B activation and interleukin-8 release in alveolar epithelial cells. 2003;302:860-864. doi:10.1016/S0006-291X(03)00224-9.

Aruoma OI, Spencer JPE, Mahmood N. Protection Against Oxidative Damage and Cell Death by the Natural Antioxidant Ergothioneine. 1999;37.

Aruoma OI, Whiteman M, England TG, Halliwell B. Antioxidant Action of Ergothioneine : Assessment of Its Ability to Scavenge Peroxynitrite. 1997;391(231):389-391.

Aubert DIRKT. Dietary Sources and Antioxidant Effects of Ergothioneine. 2007:6466-6474. doi:10.1021/jf071328f.

Benson KF, Ager DM, Landes B, Aruoma OI, Jensen GS. Improvement of joint range of motion ( ROM ) and reduction of chronic pain after consumption of an ergothioneine-containing nutritional supplement. Prev Med (Baltim). 2018;54(2012):S83-S89. doi:10.1016/j.ypmed.2012.02.001.

Betteridge, JD What Is Oxidative Stress? 2000:3-8.

Blankenfeldt W, Seebeck FP. Ergothioneine Biosynthetic Methyltransferase EgtD Reveals the Structural Basis of Aromatic Amino Acid Betaine Biosynthesis. 2015:119-125. doi:10.1002/cbic.201402522.

Cheah IK, Halliwell B. Biochimica et Biophysica Acta Ergothioneine ; antioxidant potential , physiological function and role in disease ☆. BBA – Mol Basis Dis. 2012;1822(5):784-793. doi:10.1016/j.bbadis.2011.09.017.

Chen S, Ho K, Hsieh Y, Wang L, Mau J. LWT – Food Science and Technology Contents of lovastatin , g -aminobutyric acid and ergothioneine in mushroom fruiting bodies and mycelia. LWT – Food Sci Technol. 2012;47(2):274-278. doi:10.1016/j.lwt.2012.01.019.

Deiana M, Rosa A, Casu V, et al. modulates oxidative damage in the kidney and liver of rats in vivo : studies upon the profile of polyunsaturated fatty acids L -Ergothioneine. 2004;5614:183-193. doi:10.1016/S0261-5614(03)00108-0.

Dubost NJ, Ou B, Beelman RB. Food Chemistry Quantification of polyphenols and ergothioneine in cultivated mushrooms and correlation to total antioxidant capacity. 2007;105:727-735. doi:10.1016/j.foodchem.2007.01.030.

Franzoni F, Colognato R, Galetta F, et al. An in vitro study on the free radical scavenging capacity of ergothioneine : comparison with reduced glutathione , uric acid and trolox. 2006;60:453-457. doi:10.1016/j.biopha.2006.07.015.

Gruber J, Fong S, Chen C, et al. Mitochondria-targeted antioxidants and metabolic modulators as pharmacological interventions to slow ageing. Biotechnol Adv. 2013;31(5):563-592. doi:10.1016/j.biotechadv.2012.09.005.

Gründemann D. The ergothioneine transporter controls and indicates ergothioneine activity — A review. Prev Med (Baltim). 2018;54(2012):S71-S74. doi:10.1016/j.ypmed.2011.12.001.

Halliwell B, Cheah IK, Drum CL. Biochemical and Biophysical Research Communications Ergothioneine , an adaptive antioxidant for the protection of injured tissues ? A hypothesis. Biochem Biophys Res Commun. 2016;470(2):245-250. doi:10.1016/j.bbrc.2015.12.124.

Harlfinger S, Golz S, Geerts A, et al. Discovery of the ergothioneine transporter. 2005.

Hseu Y, Lo H, Korivi M, Tsai Y, Tang M. Free Radical Biology and Medicine Dermato-protective properties of ergothioneine through induction of Nrf2 / ARE-mediated antioxidant genes in UVA-irradiated Human keratinocytes. Free Radic Biol Med. 2015;86(91):102-117. doi:10.1016/j.freeradbiomed.2015.05.026.

Kalaras MD, Richie JP, Calcagnotto A, Beelman RB. Mushrooms: A rich source of the antioxidants ergothioneine and glutathione. Food Chem. 2017;233:429-433. doi:10.1016/j.foodchem.2017.04.109.

Kerley RN, Mccarthy C, Kell DB, Kenny LC. Free Radical Biology and Medicine The potential therapeutic e ff ects of ergothioneine in pre-eclampsia. 2018;117(August 2017):145-157. doi:10.1016/j.freeradbiomed.2017.12.030.

Lee WY, Park E-J, Ahn JK, Ka K-H. Ergothioneine Contents in Fruiting Bodies and Their Enhancement in Mycelial Cultures by the Addition of Methionine. Mycobiology. 2009;37(1):43. doi:10.4489/MYCO.2009.37.1.043.

Lo Y, Lin S, Ulziijargal E, et al. Comparative Study of Contents of Several Bioactive Components in Fruiting Bodies and Mycelia of Culinary-Medicinal Mushrooms. 2012;14(4):357-363.

Li RWS, Yang C, Sit ASM, et al. Uptake and Protective Effects of Ergothioneine in Human Endothelial Cells. 2014;(September):691-700.

Markova NG, Karaman-jurukovska N, Dong KK, Damaghi N, Smiles KA, Yarosh DB. Free Radical Biology & Medicine Skin cells and tissue are capable of using L -ergothioneine as an integral component of their antioxidant defense system. Free Radic Biol Med. 2009;46(8):1168-1176. doi:10.1016/j.freeradbiomed.2009.01.021.

Martin KR. The Bioactive Agent Ergothioneine, a Key Component of Dietary Mushrooms, Inhibits Monocyte Binding to Endothelial Cells Characteristic of Early Cardiovascular Disease. 2010;13(6):1340-1346.

Moncaster JA, Walsh DT, Gentleman SM, Jen L, Aruoma OI. Ergothioneine treatment protects neurons against N -methyl- d – aspartate excitotoxicity in an in vivo rat retinal model. 2002;328:55-59.

Nakamichi N, Nakayama K, Ishimoto T, Masuo Y. Food-derived hydrophilic antioxidant ergothioneine is distributed to the brain and exerts antidepressant effect in mice. 2016;477:1-10. doi:10.1002/brb3.477.

Nguyen TH, Giri A, Ohshima T. A rapid HPLC post-column reaction analysis for the quantification of ergothioneine in edible mushrooms and in animals fed a diet supplemented with extracts from the processing waste of cultivated mushrooms. Food Chem. 2012;133(2):585-591. doi:10.1016/j.foodchem.2012.01.061.

Onofrio ND, Servillo L, Giovane A, et al. Free Radical Biology and Medicine Ergothioneine oxidation in the protection against high-glucose induced endothelial senescence : Involvement of SIRT1 and SIRT6. Free Radic Biol Med. 2016;96:211-222. doi:10.1016/j.freeradbiomed.2016.04.013.

Paul, BD, Snyder, SH. The Unusual Amino Acid, l-ergothioneine is a Physiologic Cytoprotectant. NIH public access 2010: 17-7. Doi: 10.1038/cdd.2009.163

Pizzorno, J., N.D. (2014). Glutathione! Integrative Medicine, 13(1), 8-12. Retrieved from https://search-proquest-com.buproxy.bastyr.edu/docview/1504261168?accountid=1173

Sakrak O, Kerem M, Bedirli A, et al. Ergothioneine Modulates Proinflammatory Cytokines and Heat Shock Protein 70 in Mesenteric Ischemia and Reperfusion Injury. 2018;42(2008):36-42. doi:10.1016/j.jss.2007.04.020.

Servillo L, Castaldo D, Casale R, et al. Free Radical Biology and Medicine An uncommon redox behavior sheds light on the cellular antioxidant properties of ergothioneine. Free Radic Biol Med. 2015;79:228-236. doi:10.1016/j.freeradbiomed.2014.11.017.

Shah SP, Duda JE. Dietary modifications in Parkinson ’ s disease : A neuroprotective intervention ? Med Hypotheses. 2018;85(6):1002-1005. doi:10.1016/j.mehy.2015.08.018.

Song T, Chen C, Liao J, Ou H, Tsai M. Ergothioneine protects against neuronal injury induced by cisplatin both in vitro and in vivo. Food Chem Toxicol. 2010;48(12):3492-3499. doi:10.1016/j.fct.2010.09.030.

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Wang X, Zhang J, Wu L, et al. A mini-review of chemical composition and nutritional value of edible wild-grown mushroom from China. Food Chem. 2014;151:279-285. doi:10.1016/j.foodchem.2013.11.062.

Weigand-heller AJ, Kris-etherton PM, Beelman RB. The bioavailability of ergothioneine from mushrooms ( Agaricus bisporus ) and the acute effects on antioxidant capacity and biomarkers of in fl ammation. Prev Med (Baltim). 2018;54(2012):S75-S78. doi:10.1016/j.ypmed.2011.12.028.

Wei Z, Li X, Li X, Liu Q, Cheng Y. Oxidative Stress in Parkinson ’ s Disease : A Systematic Review and. 2018;11(July):1-7. doi:10.3389/fnmol.2018.00236.

Yoshida S, Shime H, Funami K, Takaki H. The Anti-Oxidant Ergothioneine Augments the Immunomodulatory Function of TLR Agonists by Direct Action on Macrophages. 2017:1-15. doi:10.1371/journal.pone.0169360.

Zhang W, Liu Q, Zhou T, Mei B, Chen N, Jiang W. Aqueous Extraction of Ergothioneine from Mycelia of Pleurotus ostreatus and Ergothioneine Accumulation Regularity during Submerged Fermentation. Res Rev J Microbiol Biotechnol. 2016;5(1):1-8. https://www.rroij.com/open-access/aqueous-extraction-of-ergothioneine-from-mycelia-of-pleurotusostreatus-and-ergothioneine-accumulation-regularity-duringsubmerged-f-.pdf.

 

 

 

 

 

 

 

11 thoughts on “Ergothioneine: The Elusive Amino Acid

  1. Very interesting article! You are writing “Among simple mushrooms, fruiting body of White Button had the least (1.4mg erg per 85g mushroom) and Portabella the highest (2.7mg erg per 85g mushroom) based on research by Chen. What is odd is that white button and Portobello (not sure why it was called portabella above) are the same species, Agaricus bisporus, just different age groups, maybe different strains of the same species. Before Portobello became marketable all the mature button mushrooms ended up in canned soups, than cultivators started a PR campaign and marketed the mature button mushrooms as Portobello.

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  2. Thank you for this in depth and very accessible article! I have a question about the extraction. Does the hot water extraction release the ergothioneine into the water, so it is no longer held in the mycelium? Or does it break down cell walls in the mycelium to make it bioavailable when the mycelium is consumed? Basically, after the extraction would you find more ergothioneine in the water, the mycelium, or both? A 20:1 ratio of mycelium:water seems like the mycelium would not be fully submerged in water? Thank you for any help!

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    1. The ergothioneine will be in the water after extraction. If you are wanting to consume the mushroom, the best way would be to pan fry it and then you will be consuming the ergothioneine with the mushroom as food. Hope that helps!

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  3. So with the 20:1 mycelium:water extraction, since the mycelium is not submerged it’s basically just getting steamed, and all the ergothioneine is “falling” into the low water level? Is the application of heat necessary to make the ergothioneine available, or would consuming raw pleurotus hypothetically provide ergothioneine to the consumer? Thank you !!

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    1. The application of heat is not necessary. Though I would generally advise against eating raw mushrooms. I’d say the best thing to do is to make a mushroom soup, so you are consuming both the broth and mushrooms 🙂 .

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      1. Soup makes sense! I understand mushrooms should always be cooked, I’m just trying to understand what the application of hot water does molecularly to the ergothioneine in the mycelium. Ultimately I’m interested in making a medicinal preparation to have a longer lasting supply of the medicine without having to make soup. Do you know if tincture or oil extractions of pleurotus and the other fungi you mentioned also contain significant ergothioneine? Lotsa questions 😀 I appreciate your time!

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      2. You can preserve the aqueous extract containing the ergothioneine with 30% ethanol, or you can make an oyster mushroom syrup- do a strong decoction and then preserve with honey. I would do 1 part honey to 1 part aqueous extract and store in fridge. Or you can make a powdered extract..see my post on how to make your own mushroom powdered extracts.

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  4. Thank you very much for this fascinating article. I was surprised by the breath of knowledge and biochemical details abou the subject, a rare find indeed for a blog article.
    There is just a little misconception found in this otherwise excellent article, which I would like to correct: the notion that gilled mushrooms generally contain more ergothioneine than polyphores. Indeed, Agaricus mushrooms are among the edible mushrooms containing the least ergothioneine, while the Boletales contain by far the highest amounts – between 100 and 1000 times more than Agaricus. Among the gilleed mushrooms however, Pleurotaceae stick out with amounts comparable to the Boletales. See this article for a comprehensive table of the ergothioneine content of different mushroom species and parts:
    https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/ergothioneine

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    1. Thank you for your response! I should have been more clear – I was referring to the woody medicinal polypores that are the most commonly applauded Polypore mushrooms and the ones I am apt to write about most. Didn’t mean to leave out the lovely boletes.

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