I get so excited seeing Uni-level stuff that I've done being actively supported and disseminated on youtube! I get so excitd i want to comment in the first 5 minutes of videos but always wait lol
@FreshfromtheFarmFungi2 жыл бұрын
comment away sir! Thanks for watching
@AntiTrollable3 жыл бұрын
Thank you, you sparked my interest and I will be experimenting with your techniques to create new genetic strains. It's crazy that you are the only person on KZbin who talks about this amazing process. Who would have thought haploid only has one chromosome set and we have the ability to create 2 complete chromosome sets. SO MUCH FUN!
@geinstein84074 жыл бұрын
OK coming from a small business owner making spawn, some one in mycology for 6 years and some some who have gone through almost everyone on KZbin with mycology I take my hat of for you, your methods for explaining is the simplest and easiest
@FreshfromtheFarmFungi4 жыл бұрын
Thanks I appreciate it! Thanks for watching! Coming from someone with so much experience - is there any topic that is being ignored that I should be covering? MUSHLOVE
@geinstein84074 жыл бұрын
@@FreshfromtheFarmFungi Actually yes the exact topics your handling I haven't watched all of your videos yes but there all really good Again I take my hat off for you
@mikerizzyraw3 жыл бұрын
Fresh from the Farm Fungi LLC .. thanks love these breeding videos, if you ever get time, would love to see any microscopy techniques, such as verifying isolates, and dikaryon crosses; or doing it with pcr. long term storage like using nitrogen or glycerin ect... would be good too. I can only find this info google scholar.
@geinstein84073 жыл бұрын
@@mikerizzyraw I actually think this guy is so great he might even be heading/ showing that stuff soon regardless of asking Again I really love this guys videos
@FreshfromtheFarmFungi4 жыл бұрын
Thank you everyone now go out there and breed some cool strains! MUSHLOVE
@kodyfrost4 жыл бұрын
Building my little myco-corner right now. Can't wait to finally get started. Been doing a lot of research and am ready to get my hands dirty so to speak
@Jason-uh7ml3 жыл бұрын
Does this mean you get to name it🤔
@jidun94783 жыл бұрын
I really appreciate this thorough and methodical display of the practice, thank you!
@Spark_Books Жыл бұрын
This is ART, Mr. White!
@twtech4 жыл бұрын
This is incredible knowledge you are sharing. I've got what I need now to get started on something I've wondered about for months. Thank you!
@Man-EatingMushroom3 жыл бұрын
Damn your good bro! Your agar process may be the tidiest and quickest I’ve seen yet.
@shainemaine12682 жыл бұрын
17:56 the one time you didn't get it perfect is how my transfers look everytime hahaha
@FreshfromtheFarmFungi2 жыл бұрын
it takes lots of practice and I still am improving - can’t wait to look back in 30 years and see the differences
@kodyfrost4 жыл бұрын
Iv been waiting for this day
@robertgould18684 жыл бұрын
Thanks for this Gary! Super interesting and exciting stuff.
@TheEricFlu4 жыл бұрын
Keep the videos coming. Thank you.
@ArchersMushrooms4 жыл бұрын
Absolutely awesome mate. Thank you so much for putting this stuff out. Absolute quality!
@Alpha_fitz Жыл бұрын
We're all very excited about your chestnuts too.
@Bootydoc19993 жыл бұрын
Love it. Thank you for your generosity and time
@allennichols58562 жыл бұрын
Hey Gary - thanks so much for sharing this! I am bout to nerd out like a boss! 😜😆
@endothermicEnigma2 жыл бұрын
Shhhhhh... you're upsetting the agar...
@kathyanne35874 жыл бұрын
Gary , wonderful Video, i love your organization. you make it seem very easy. THANK YOU
@adambinx97014 жыл бұрын
Thank you for sharing your knowledge!!
@DIEZELQUAY2 жыл бұрын
Gary, you are the man. Thanks for all the kick ass videos. I'm learning a phenomenal amount. Good karma for FFTFF!
@carlosbello62143 жыл бұрын
Good information, grettings from Chile!🇨🇱
@soccer2themax3 жыл бұрын
Thank you for putting this content out here.
@BigfootPrintingАй бұрын
Hey Gary, I’ve really been enjoying these videos. You seem to be extremely well educated and a good presenter. May I ask if you know of any books or other robust resources that I could study to learn about this genetic/breeding/microbiology stuff pertaining to our mycology contexts? KZbin is a great resource, but I really like an authoritative sources like books
@Wavy_Gravy Жыл бұрын
Not me dreaming of breeding mushrooms in the mountains for the rest of my life lol.
@vanniyo8988 Жыл бұрын
I think the term is eukaryotic and dikaryotic mean single celled nucleus and double celled nucleus.
@hvfd12213 жыл бұрын
Thank you for sharing your knowledge! I cant wait to try this.
@FreshfromtheFarmFungi3 жыл бұрын
Thanks for watching and following along! 🍄❤️
@summersummer12327 сағат бұрын
Can you just "mate" them when you transfer the agar to spawn bags? i.e. cut up the agar dishes and add at least two types into the same spawn bag?
@Mycomania697 ай бұрын
Awesome video!
@bluebowser31212 жыл бұрын
Please do a video hybridizing yellow and pink oyster mushrooms!!
@bluebowser31212 жыл бұрын
I think you're doing that in the video actually. Your use of certain words just throws me off completely. I'm not a scientist.
@FreshfromtheFarmFungi2 жыл бұрын
check out this video kzbin.info/www/bejne/iWmUpYCCasSFY6c
@stefandomagalski37223 жыл бұрын
Beautiful! Thank you!
@ovechristophermattmann8802 жыл бұрын
Hey! I was wondering. Do you also do this for your Cordyceps?
@Chris.Crayos.dnb.2 жыл бұрын
I think this is the way to cross cordyceps genetics to create new strain lineages. Shouldn't matter what Mushroom it is. Should work for all of them ^^
@TheSaltPrincess2 жыл бұрын
This video got me price checking pyrex petri dishes
@CHIROTHECA2 жыл бұрын
Great!
@michaelmcnulty18753 жыл бұрын
This makes me wonder if a microtubulin inhibitor like oryzalin could produce polyploid fungi.
@FreshfromtheFarmFungi3 жыл бұрын
not sure but interested! 👍
@DIEZELQUAY2 жыл бұрын
I've got oryzalin and was wondering this myself. What would be the best practice for this? Any recommendations?
@ericchurchill84022 жыл бұрын
Nice
@niknik7470 Жыл бұрын
Ol big brain over here flexing. Many thanks homie 🤙
@jordanjacobs29904 жыл бұрын
Hey, Thanks for this! quick question - How can I tell if my culture is haploid or diploid without a microscope?
@FreshfromtheFarmFungi4 жыл бұрын
Jordan Jacobs If you fruit it out then it is diploid (some exceptions) Also, if it came from a single spore then it is haploid. In order to obtain a single spore isolate, one should perform serial dilutions and quantitate the spore load/viability and then isolate single spore colonies. Also, genetic testing can be performed (PCR or Gene Sequencing)
@CMZneu3 жыл бұрын
@@FreshfromtheFarmFungi Not an expert but i think under a microscope you should only see clamp connections in diploid(mated) mycelium but i'm sure there are exceptions.
@cjjamieson14 күн бұрын
Do you get a new blade every time instead of applying a flame to it?
@FreshfromtheFarmFungi14 күн бұрын
for breeding yes - if I use a mono culture I will flame but since it’s so sensitive I want to make sure there is no carryover
@danjf12 жыл бұрын
instead of using all those scael blades couldn't you have used flame to sterilize 1 blade? ty
@FreshfromtheFarmFungi2 жыл бұрын
Yes I wanted to guarantee sterility and prefer the sharper blades, but I do flame sterilize sometimes for inoculations
@BOOYAGA4 жыл бұрын
I hate how life doesn't allow me to be first on these videos 😅
@apkeeney3 жыл бұрын
This is awesome... thank you!
@LarsLarsen776 ай бұрын
Bro, you really counted all the permutations? There's a whole field of math called combinatorics and you can calculate that with a simple equation: N x (N-1) / 2
@JonLuk412 жыл бұрын
Very helpful!
@MycoDogs Жыл бұрын
Do you look for clamp connections under a microscope to make sure u have monokaryotic isolates before introducing them together? Or do u not find it necessary
@shanesmith894 жыл бұрын
Who taught you all of this? very cool
@FreshfromtheFarmFungi4 жыл бұрын
S Smith I have read a lot of literature and been performing tissue culture for a long time - Also, have a background in clinical mycology/microbiology. I recommend any Paul Stamets books, Tradd Cotter and Peter McCoy have great books as well on mycology - MUSHLOVE
@DrMonochrome3 жыл бұрын
This is how you cross breed lots of different isolates of sepperate strains, love the lab coat and the apple earphone but you're not fooling me. Using 6 different scalpels when you could have used one and flame sterilized it each time which is what you should be doing if you hope to achieve selecting isolates from the agar...
@FreshfromtheFarmFungi3 жыл бұрын
I have yet to purchase a bacticinerator which I would use, but am against open flames since it’s my own lab and operation. For safety reasons I prefer to use a fresh blade each time and get it into liquid culture as soon as possible 👍 MUSHLOVE
@SERGEYFTАй бұрын
Do Cordyceps militaris spores last long? Can you use them to make a spore print on foil and store it for years? Or should the spores be planted immediately since their shelf life is short?
@FreshfromtheFarmFungiАй бұрын
the cordyceps spores are ascospores and are fragile so they should be used fresh as quickly as possible
@sleepyowl910 Жыл бұрын
Does each dish with isolates contain dikaryotic mycelium? Looks like those mycelia in dishes come from mushroom body fragments, not spores.
@CMZneu3 жыл бұрын
Great video! Quick question will Haploid and Diploid Mycelium act and look the same if grow out the only difference being one can produce fruit? Is there like a certain distance a Haploid can grow out looking for a mate before it stalls or looses viggor? to the naked eye do both behave and look the same and there is no way to tell one from the other?
@FreshfromtheFarmFungi3 жыл бұрын
It can behave and look the same - you can do genetic analysis to differentiate them before fruiting but it’s cheaper and easier in my opinion to just fruit them out unless you have access to PCR, extraction equipment and a way to read and compare genomic sequences
@thomasreto29974 жыл бұрын
Great content. Thanks for the time🌈😃🤙
@jasonmillar26262 жыл бұрын
Please could you explain how that is haploid?
@13thbiosphere2 жыл бұрын
Providing a link to the conclusion that would be good idea
@FreshfromtheFarmFungi2 жыл бұрын
kzbin.info/www/bejne/qpy6pKlrepqgY5o
@efsanekral2892 Жыл бұрын
Is this the morel mushroom production process?
@FreshfromtheFarmFungi Жыл бұрын
for cordyceps
@HellGod67 Жыл бұрын
Hello! Do you think this is possible to do in a still air box?
@cdurch1 Жыл бұрын
I've been doing it in open air n into 2oz clear ketchup cups with snap on lids. Small bathroom, no air movement hvac is off, gloves, iso, mask... most importantly you first spray superfine mist of water into corners of room and all around. The mist dropping to ground removes many contaminates from air. I next spray similarly with ISO (careful, you do still need to breath, 😆). Really get all air in small room, from top to bottom, misted to drop all contaminates. This is after I've got everything set up and I'm place. Using this method, I've been having great success with spore to agar cup as well as spore syringe to agar. No contaminants yet from almost 40 agar cups over last 2 months, and I've even been able to innoculate grain and LC jars from agar growths, etc. I did have contamination when I tried to innoculate LC with clone tissue. Both LC went cloudy and had contams. 😢 But I've got 7 other LC from spore syringe and, agar inoculations that are doing great. So... it can be done without laminar hood, it can be done without SAB. Just be sure to wipe and spray with ISO a LOT
@kingsrex6228 Жыл бұрын
How can I modify the genetics of my mushroom?
@FreshfromtheFarmFungi Жыл бұрын
there are many techniques- spore breeding, di-mon mating, crispr cas9, physical and chemical mutations. All these require extensive laboratory procedures
@jasonsimmons43194 жыл бұрын
Let me get some things straight, why are you assuming these are haploid isolates? As far as i can tell you just streaked out from serial dilution and the thing with mushroom spores is they stick.. so chances are each of those colonies are actually dikaryotic (not diploid like you said) unless you confirmed they were single spores through microscopy. How are you confirming these were actually single spored
@CMZneu3 жыл бұрын
Exactly
@KidCharlema9ne3 жыл бұрын
Agreed.. besides the fact that I just watched agar transfers for 22 minutes.
@FreshfromtheFarmFungi2 жыл бұрын
watch the playlist kzbin.info/aero/PLFfnF_UJ5WgKRxZZbixO27fxOi9mEtmTv Also, you can add polysorbate 20 to help prevent them from sticking together - I do this in the latest videos it’s much more clear. The best way to confirm is cross them and fruit them we got really good results in the next videos. Microscopy won’t help verify either, most strains do not form clamp connections and it’s pretty subjective under a scope which is why Im trying to explain without one. I will elaborate once I get better equipment this is the easiest low-cost way to isolate spores
@Drum3Matrix2 жыл бұрын
How do you know if you have a haploid though what if two spores just stuck together after diluting and you didn't know? Can you tell?
@FreshfromtheFarmFungi2 жыл бұрын
genetic testing would confirm but otherwise just growing it out is the best way - imagine it as strawberry plants that had to meet - there would be patches with berries and patches without so you could decipher
@davegrad3802 Жыл бұрын
Yeah, I'm so lost.
@terracotta101 Жыл бұрын
Will you take a transfer of the mated diploids and let that grow out or just put the diploid plate straight to grain? And what do you do w/ the plates that don't mate and remain haploid?
@ticklememary9922 жыл бұрын
you don't ever worry about contam with handling those with bare hands?
@FreshfromtheFarmFungi2 жыл бұрын
It’s not the best practice but for learning purposes it doesn’t matter - for production it is much more stringent
@ticklememary9922 жыл бұрын
@@FreshfromtheFarmFungi appreciate the response. I've recently been getting mold on few plates after getting back into agar..showing friends and family etc.. i've been told is likely due to over-handling.
@alanking42043 жыл бұрын
It would help if you showed some results of your experiments
@FreshfromtheFarmFungi2 жыл бұрын
they make it all the way - follow these videos on the playlist “breeding mushrooms from spores” kzbin.info/aero/PLFfnF_UJ5WgKRxZZbixO27fxOi9mEtmTv
@vitaly52092 жыл бұрын
so that means mushroom throwing spores and they creating haploid colonies then finding each other and create new diploin breed ready for fruiting, right?can we say that diploid colony needed for mycilium to fruit? thank you so much! i'm really appreciate you sharing such information
@FreshfromtheFarmFungi2 жыл бұрын
yes that is correct for the most part! Some exceptions exist but that’s the rule of thumb for most species
@Robebabu2 жыл бұрын
Is there an ideal amount of space to leave between transfers for them to grow into? Or could they be placed directly next to each other in hopes that they find each other and mate sooner, leaving more room for peripheral growth?
@FreshfromtheFarmFungi2 жыл бұрын
it is important to see if there is a zone of inhibition for non-mating pairs so I wouldn’t place them right next to eachother
@BOOYAGA4 жыл бұрын
I hate to nag, but could you do a lab walk through, with afterthoughts? I'm starting my basement lab and would like tips from someone that's proven successful 👍 I've gotten a reply in regards to the flow hoods too, prices were on point 😊 what width is yours?
@FreshfromtheFarmFungi4 жыл бұрын
Motor Miljø Thanks for following along - I will see what we can do - the lab here is less than ideal and I recommend reading up on Paul Stamets’ literature (Mushroom cultivar and How to grow gourmet and medicinal mushrooms are the go-to guides in mycology) Also, Tradd Cotter’s book and Peter McCoy’s Radical Mycology are great for the technical and more experimental aspects in growing - these books have helped shaped our processes and provide a deeper insight into designing a lab/system that will fit your needs - MUSHLOVE P.S. Our hood is 8ft dual filter
@donnbialik90852 жыл бұрын
Do you do microscopy to confirm monokaryons?
@FreshfromtheFarmFungi2 жыл бұрын
microscopy would not confirm - clamp connections are subjective only genetic testing and growing them out confirms 100%
@BOOYAGA4 жыл бұрын
Also, is there a rule of thumb in regards to what species will mix?
@FreshfromtheFarmFungi4 жыл бұрын
Motor Miljø We are always tinkering with the “rules of thumbs” hah experimentation is key! However, in nature, like species mate with like species until small mutations occur and develop sub-species which later become their own species living in their niche
@quinxx122 жыл бұрын
Great content, but honestly I wouldn't waste so many blades. Just flae-sterilize the quickly or with ethanol.
@DIEZELQUAY2 жыл бұрын
When you weigh sterility x $5 pack of 10 blades w/handle, It's just not worth the risk to waste time with contaminants
@shainemaine12682 жыл бұрын
Have anything against high-temp sterilizing your blade and just using one?
@FreshfromtheFarmFungi2 жыл бұрын
I don’t like open flames and prefer the sharp clean cuts of a new blade. I do have a torch for loops now but prefer new blades especially when breeding to ensure sterility and prevent any cross contam. It’s a higher standard
@benredbeard70233 жыл бұрын
OK the numbers are the order in which they formed the colony, what is the letter code?
@FreshfromtheFarmFungi3 жыл бұрын
the letters are indicating the plate of origin from the dilutions
@UnsolvedAz233 жыл бұрын
are the isolates you are working with in this video the same spore dilution plates from video one feels like I skipped a step or video
@FreshfromtheFarmFungi2 жыл бұрын
yes they are the same ones follow the playlist “breeding mushrooms from spores” kzbin.info/aero/PLFfnF_UJ5WgKRxZZbixO27fxOi9mEtmTv
@ShotgunLlama Жыл бұрын
I'm still unclear on how you made sure the haploids were truly single haploids and not 2 or more or already fused diploids. Did you just lower the concentration of spores so much that they were too dilute in your streaks to meet and fuse before you separated them?
@FreshfromtheFarmFungi Жыл бұрын
yes please watch part 1 it will make more sense
@ShotgunLlama Жыл бұрын
@@FreshfromtheFarmFungi I did watch part 1. I left this comment after watching both parts
@efsanekral2892 Жыл бұрын
what are the materials used
@FreshfromtheFarmFungi Жыл бұрын
it is agar (MEA) and petri dishes
@galbois34962 жыл бұрын
I want to know these referrals and their amounts?
@kieranconnell7602 жыл бұрын
Is every colony from spore plate from streaked solution a haploid colony definitely?
@FreshfromtheFarmFungi2 жыл бұрын
not definitely until it is crossed and grown out. There is a chance two spores can stick together or germinate very close and the only way to know for sure is to grow them out or do genetic testing
@kieranconnell7602 жыл бұрын
@@FreshfromtheFarmFungi thanks so much for the swift response. But both haploid and diploid mycelium can fruit? I understood from multi spore I was trying to separate the mycelium to somehow isolate it. Then see if that would fruit. Do I now understand I should make pairings of all the transfers from the multispore plate ? Then fruit ones which combine and create diploid mycelium .or is this essentially pointless without your early extraction of colonies because I can't really know if my plates are infact haploid? I hope that make sense ? 🙏
@kieranconnell7602 жыл бұрын
I often come to a place with people in my line of questioning and hear you even say sometimes that it's purely chance and choice really. And essentially it's much simpler to fruit and clone a phenotype ,so why go through such a process for another phenotype? Maybe I missed in this video but what makes it better that it's worth this or its for the science and exploration. ?
@ZaneofAustin3 жыл бұрын
this is just a random question im sure you get all the time definately in the mindset of coulda not shoulda but could you cross breed say pink oyster and a cubensis variety? would they even be able to breed? for purely scientific purposes of course
@FreshfromtheFarmFungi3 жыл бұрын
I think anything is possible - I have heard of people using snake venom to hybridize different mushrooms strains but am not very familiar with that procedure - but it’s out there somewhere 🙂❤️🍄
@jakelancaster58893 жыл бұрын
What type of agar is that? It's so pretty
@FreshfromtheFarmFungi3 жыл бұрын
MEA (malt extract agar)
@smithsmith81193 жыл бұрын
How do you know its a haploid, and two didn't mate? Is it very obvious? Does the look vary wildly across species? Thanks
@FreshfromtheFarmFungi2 жыл бұрын
it’s not very obvious without fruiting them out - there is some variation yes but it needs to be crossed and fruited to verify
@kumabjorn79923 жыл бұрын
18:55 yeah close call. I even held my breath when I saw that slip.
@KidCharlema9ne3 жыл бұрын
Question - that was a pretty big gap between video 1 and 2 - how did you isolate the haploid mycelium and know it was haploid? I saw you mention in another question that you either have to fruit it out or genetic sequence. Which did you do? Seems like a lot of work/waste to "fruit" stuff out to see if it doesn't fruit to make sure it's hapoid, especially when you know nothing else about the strain.
@cullsans3 жыл бұрын
In the first video he diluted the spore solutions which I believe is key to the process by ensuring you get roughly 10 (numbers may be way off) spores/plate. This ensures you are getting haploids whereas when you scrape thousands of spores onto a plate it is more of a free for all. This was my interpretation anyway!
@FreshfromtheFarmFungi2 жыл бұрын
kzbin.info/aero/PLFfnF_UJ5WgKRxZZbixO27fxOi9mEtmTv watch this playlist - yes it is very wasteful but it’s still the best way because once you find a good one you can keep the haploid and cross again. The hard part is finding them
@FreshfromtheFarmFungi2 жыл бұрын
yes exactly
@vitaly52093 жыл бұрын
Good job! Please can you tell me souce where I can find information about making powerful mycelium with good crop. I know how to make pure culture on agar media from spor or tissue but how I can know that it's profitable strain?
@soccer2themax3 жыл бұрын
A lot of it is getting a feel for what is good growth and what is not. Just keep experimenting and observing. Remembering and learning. These videos are really nice because he shows you the growth and talks about it, so you can get a few looks at good stuff here.
@FreshfromtheFarmFungi2 жыл бұрын
it is hard to know before you fruit it out - start with some strong cultures we sell ours here etsy.com/shop/freshfungi
@rockskipper53532 жыл бұрын
I think I'm finding out that the cotton looking mycelium is from too much moisture . And the (slow growth/growing more in a mound /not stretching) is because u have too much nutrients for the mycelium to eat
@FreshfromtheFarmFungi2 жыл бұрын
it may be that but I have seen rizomorphic mycelium in the same conditions so some mycelium may be more susceptible than others to these morphologies 🍄❤️
@rockskipper53532 жыл бұрын
@@FreshfromtheFarmFungi I can agree with that ... some times u will plant a seed and the plant pops up deformed.. I'm sure the same thing happens with fungi
@g-lurk Жыл бұрын
is diploid mycelium and dikaryotic mycelium interchangeable?
@FreshfromtheFarmFungi Жыл бұрын
Dikariotic refers to the nucleus (two nuclei), diploid refers to the genetic information required to produce a viable ascospore or basidiospore - they are relatively the same but slightly different. At least from my understanding
@g-lurk Жыл бұрын
@@FreshfromtheFarmFungi with every question answered i get at least one more! but anyway, this is helpful, thanks a lot for taking the time, Gary! MUSH Love!
@siddiquewadiwala37603 жыл бұрын
What results of isolation in part 1?
@FreshfromtheFarmFungi2 жыл бұрын
kzbin.info/aero/PLFfnF_UJ5WgKRxZZbixO27fxOi9mEtmTv watch this playlist it explains all
@Section8_Inc2 жыл бұрын
what did you seal your dishes with?
@FreshfromtheFarmFungi2 жыл бұрын
parafilm
@SweetLife5294 жыл бұрын
Can you ship to Canada?
@FreshfromtheFarmFungi4 жыл бұрын
Sweet Life 529 We only ship within the US right now
@SweetLife5294 жыл бұрын
Fresh from the Farm Fungi LLC , yeah.....to bad! Would love to order some Chestnuts!
@user-og7wc1ks3z2 жыл бұрын
Отлично брат, ты супер!!!
@jonnypage94842 жыл бұрын
God I'm really scratching my head right now . So I'm watching your videos in for some reason I'm having a hard time grasping and taking it all in maybe I'm stressed. And I've been looking up a lot of research on you know mixing mushrooms and some people say snake that some are even saying utilizing penicillin I believe. I was watching one of your videos and I'm not sure if I grasped it right but it seems like you were taking two different species putting them inside the same petri dish and if the mycelium (connected in the middle You're taking a sample from the connection) And if the two mycelium mats were not compatible clearly divide down the middle. Now with that being said let's say I wanted to crossbreed Panaeolus cyanescens with something like albino penis envy. Could I just take the two mycelium grow them out in the dish and And if it connects in the middle take a sample and put it into a different dish and then grow it out? My question is from that connection sample from ape an pan can is there a chance I could crossbreed or make a hybrid penis envy/pan . Or I might just completely wrong about why you are putting two different mycelial mats together hoping for a connection? I'm sorry I'm just trying to take this all in
@FreshfromtheFarmFungi2 жыл бұрын
These spores are from the same species and each spore contains half of the genetics needed to fruit out a mushroom successfully- that being said there are many theoretical and some proven methods of hybridization between different species but it’s much more complex and less likely to result in successful pairing. Hope that makes sense - I don’t want to discourage people from trying anything but this method described in this series is within the same species.
@Angelina-xj5zd2 жыл бұрын
Meow.
@danielboomers2 жыл бұрын
biggest waste of plastic and blades... use pp5 dishes and reuse them !!!
@FreshfromtheFarmFungi2 жыл бұрын
For someone with plenty of time and does small production I agree - this may be overkill. For someone seriously relying on sterility and efficiency, this is a better method. 🍄❤️
@danielboomers2 жыл бұрын
@@FreshfromtheFarmFungi efficiency yes....sterile no way... never ever i had problem with pp5 agar dishes .. and they are reusable many many times over.. we waste to much plastic... you also could go for glass petrie dishes...
@NoBody420Psilocybin Жыл бұрын
I heard genetics can't cross that way.
@FreshfromtheFarmFungi Жыл бұрын
The science has been there for decades lol - Look up “Monokaryon mating in filamentous fungi” you will find your answers
@brutalblends9283 жыл бұрын
and you should close your petri dishes between transfers
@darrenfulwood37663 жыл бұрын
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@theghostofsw62763 жыл бұрын
Damn....what happened to this guy's flow hood? Looks like someone kicked the livin' shit out of it. Disgruntled employee? Bad day at the office? Too much whiskey at the staff Christmas party? 6:01
@FreshfromtheFarmFungi3 жыл бұрын
Ha good observation the cracking is from cooling off substrate blocks stacked up against the plexiglass - caused it to expand and contract and well, crack - we are planning to upgrade the housing to stainless steel when the season slows down 👍😎
@theghostofsw62763 жыл бұрын
@@FreshfromtheFarmFungi Hahaha.....I was just razzin' you a bit. Whatever gets the job done, buddy....that's all that counts. Cheers!
@zuul9023 жыл бұрын
dude, you really need to try and practice more sustainable less wasteful methods. I appreciate your videos, but the amount of plastic waste is just ridiculous
@FreshfromtheFarmFungi3 жыл бұрын
I appreciate this concern and will try to think of something better for this winter
@zuul9023 жыл бұрын
@@FreshfromtheFarmFungi thanks for taking the time to read this and respond 😁 sorry, I don't mean to come off negatively in any way. You make great videos!
@mycomachine94883 жыл бұрын
@@zuul902 how exactly would you go about reducing the number of plates based on the number of isolates and transfer requirements? Split plates maybe 🤔 but that doesn’t seem viable.