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Re: AGAR ENVY! (Anything and All things agar!) [Re: Rasmodius]
    #29588900 -

I honestly don’t think those bits are supposed to be there on the atl plates, possible contam. Am I fucked ?

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Re: AGAR ENVY! (Anything and All things agar!) [Re: bluescreen] * 1
    #29588912 -

Like you, i get way better growth with PDA than LME so I just stopped pouring malt plates and only use that stuff for liquid culture. I also get better clarity and less clumping with PDA.

The only area lme is superior at is price, but imo the extra cost for the lab grade PDA mix is worth it

If you're dead set on using the lme though maybe try using less nutrients. That's where I was at on my chase down the rabbit hole before I said fuck it and gave up. Maybe make up a few batches of LME with different nutrient profiles and compare growth directly. And share the results with the class of course c:


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Re: AGAR ENVY! (Anything and All things agar!) [Re: Anomalocaris]
    #29588914 -

Wow, thanks for sharing!

I'm a slut for clean plates. Those are gorgeous

Tbh sometimes I think I enjoy the agar part and taking pics more than the mushroom growing part

Quote:
Anomalocaris said:]

Mix of a few cool looking ones.


You likey?



I like all three of these for different reasons, but that middle one is boner- inducing.

Good Lord

:hotdamn:


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Re: AGAR ENVY! (Anything and All things agar!) [Re: Archespore]
    #29588918 -

How are these plates looking? I’m some of the plates the surface growth looks whispy almost clear and I’m some is very apparent and white. I can see growth rings and it’s clear and I’m assuming it’s because the mycelium is digesting the dye. I only used like 5ml of corn syrup to 300 Ml of water. I made a new batch with no color so we’ll see but is that normal and do they look fine



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Re: AGAR ENVY! (Anything and All things agar!) [Re: Awfullotofshrooms]
    #29588921 -

Hey buddy, I can see your fingerprints in way higher detail than the mycelium in that first pic. The middle one is alright

Can you manually adjust the focus and upload a couple more shots? It looks like you've got a high quality camera but maybe the focus is just a little bit off

From what I can see, I'd recommend taking another transfer asap. Also maybe try using smaller wedges? Easier to identify uniform growth from smaller transfers

And yea, it's normal for the myc to suck up the dye. Also I have fucked around with lots of different dyes and anything that has red or yellow in it consistently performed worse than those with no dye or blue only.

Of course other people around here have beautiful strong growth on blood red plates so... Grain of salt and all that


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Re: AGAR ENVY! (Anything and All things agar!) [Re: Archespore] * 1
    #29588924 -

Will do captain 👩‍✈️ I won’t let you down. Will report soon

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Awfullotofshrooms]
    #29589017 -

is my recipe too high in nutes? got good regular growth for multipsore its just so deep in the agar. I believe I used too much agar mix? its a premixed bag of MEA I bought from some Amazon vendor, tried finding seaweed labs or whatever from years ago but couldn't find em










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REPENT

Edited by jbgtaa (05/28/26 07:27 PM)

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Archespore]
    #29589020 -

Here’s a couple fronts and backs










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Re: AGAR ENVY! (Anything and All things agar!) [Re: Tormato]
    #29589054 -

I already posted these on my main growers log thread, but I'll post them here for a quicker answer (and also because I want to ask a question related to making no pour plates. I know one of the white plates has tam on it but also has quite a lot of good stuff around it.












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Take me back to November
Hawaiian shirts in the winter, deep thoughts, deep thoughts
Naw, take me back to November, wassup

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Doctor_Doggo]
    #29589153 -

Can you open them? I cant really tell what is actually going on because the color of the agar and the thick glass

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Doctor_Doggo]
    #29589157 -






And here's the last of them. Now, my question when it comes to making no pour plates.

I am currently using unmodified lids with these instead of the typical hole + micropore tape combo because my plates flooded during my first run with them, and after putting two and two together (and being told so) that unsealing them and having the vaccum break leads to contamination.

I've heard some people flip the lids (still unmodified) over to not make a seal and use those, but I've heard they are also inconsistent for working without contamination. I would like to do more with micropore tape lids but I want to use less materials, so I'd like to know if polyfill and SFD lids would work instead of micropore tape lids. And if they do, would I still need to wrap them with foil before PCing them?

Thanks for the answers and info. Mush love <3


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Take me back to November
Hawaiian shirts in the winter, deep thoughts, deep thoughts
Naw, take me back to November, wassup

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Re: AGAR ENVY! (Anything and All things agar!) [Re: CocaineBuffet]
    #29589158 -

I do not have time tonight but I will tomorrow.


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Take me back to November
Hawaiian shirts in the winter, deep thoughts, deep thoughts
Naw, take me back to November, wassup

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Anomalocaris] * 6
    #29589173 -

Anomalocaris said:
Some cool plates for the agar enjoyers

Some Pan Cyan TTBVI. Amazing looking stuff!








Different ttbvi genetic:



Pan Cyan Estero


Pan Bisporus, very thin mycelium!


Penis envy uncut


Mix of a few cool looking ones.


You likey?



Hate to be the bearer of bad news but just from the pics, most if not all of those pan plates are infected with bacteria.  It’s a very very common bacteria that’s probably present in most mushroom grows but is only detrimental to less hardy mycelium species like pan cyans.  It’s that orange/brown/yellow/reddish tint you see on your plates. 

I’ve spent the last 7ish months trying to get rid of it in my cultures and it will not be extinguished through normal means of transferring away or cabin sequesters or pucks or really anything “normal”

I don’t know for sure but I believe it’s Serratia marcescens which is the bacteria that produces that pinkish hue around sinks and drains in bathrooms.  From everything I’ve read, it fits the description.  It’s very light so it’s airborne.  Strains of it can be translucent so you won’t even see it unless it builds up or the only time you will know you have it is because of how the culture starts acting.  It’s motile and can do something on agar plates called “swarming”.  It’s extremely fast.  It’ll keep up with pan myc and eventually outrun it.  It’s very hard to see on low nute agar <1%

If you take ANY agar with a transfer off an infected plate.. like the tiniest bit off the very leading edge, you’ll 100% take the bacteria with it.  The best chance you have at getting any kind of culture that might give decent results is to take aerial hyphae only off the leading edge.. like the tiniest bit you can manage using either a hooked scalpel or a very sharp needle (being careful not to dip it into the culture as much as possible.)

Here’s some examples of it in action..

So you’d look at these two cultures and think, “they look pretty decent, fully grown out.. aerial surface myc the whole way”..  (you can see the transfer in the middle is the tiniest bit of myc.. I scraped that off the very top of a leading edge of aerial myc on a donor plate



But then you turn the plate(s) around..



In the first pic ^^^, the yellowish tint is very faint around transfer and in the second pic, it’s more pronounced and fills out more.. those cultures are both fully infected.  The only reason you can see it in the middle is because that’s where it started and slowly builds up to the point of being visual.

Sometimes you can’t even see it plainly like that.  Your culture will just start acting fucked up.. the leading edge will cease to grow aerial myc and the mycelium will burrow down into the agar.  Here’s the beginning of that without the obvious brown/yellow lines


Here you can see where the leading edge has stopped and growth has continued inside the agar without aerial growth.. you can see the line of brown tint (actually when you really get close up on it with a bright light IRL, it’s more of a color band with layers of orange, yellow and red)


I think this is where the bacteria has outran the leading edge and the myc is actually following the bacteria inside the agar.  Idk any of this for fact, this is just what I’ve come to after looking at 100’s of plates with this shit on it. 

More examples of the leading edge starting to crash out


Before I stopped taking pieces of agar with my transfers (like tiny pieces of leading edge agar with the smallest bit of myc on it) and switching to aerial myc only, this is what my plates would end up looking like..


The shit is brutal.  Because it’s light and airborne, it easily infects an entire plate culture and is known (Serratia marcescens) to migrate on the tops of cultures so, as you can see, even taking aerial myc isn’t fully effective.

I’ve been using gentamicin antibiotics and the first round I did, I added pre sterilization… gentamicin is heat stable but degrades at prolonged times at those high temperatures.  The next round i did, I did syringe filter “sterilizing” where I added during the cool down before pour.  I’m hoping this makes the antibiotics more effective.  I did see some improvement the first round but not enough.

I’m also trying syringe filtered h2o2 soaks of my plates and taking small transfers of myc only from the soaks.. this is showing a lot of promise but I think I may need to do multiple rounds

The good news is that aggressive varieties/cultures can manage even being infected with it.  It’s so common.. in fact, I’ve seen it on almost every pan print I’ve gotten from someone else.. it’s in my own prints, especially anything I’ve taken from the jcm, which is most of them. 

I believe it’s the reason we mostly only see aggressive varieties in circulation.  Ttbvi, MiB, Texas etc.  it’s a weak infection to these aggressive vars.  I also think it’s why poor first flushes are commonly reported and then later flushes get better.  Substrates seem to “overcome” the weak infection.  It’s why less aggressive cultures don’t recover from a shake.  Ik there’s other factors too but this bacteria is so common and ungodly persistent.

A lot of ppl say they get those brown streaks and just ignore them and they’re grows aren’t affected… I think they are affected, I just think they have very aggressive and strong genetics and if they were to rid those cultures of the infection, their cultures would perform even better. 

For example, this plate..


Gave three flushes.  First one was shit.  Second one was a little better and then the third was this


All these grows were infected with the same bacteria… all gave poor first flushes with each subsequent one getting better and better


Pretty much any grow I’ve done in the last 8 months was the same.  And those are the ones that actually made it to fruiting… I’ve thrown away so many trays that never made it to fruiting because of this facking bacteria.  The one thing that all the trays that made it had in common was that they were aggressive varieties/cultures.

Again, this is all just what I’ve come to accept in my own growing experience with pans so take it with a grain of salt but I think it’s this one bacteria that makes growing pans difficult

@OP. You see these brown spots on your transfer in this pic?


That’s a pretty good sign that plate is infected

More examples… it really likes grain water agar.  Sometimes it shows up very pronounced


Sometimes it’s only noticeable if you really look hard.  This plate is also gwa and looks aight (the pink is the reflection of my finger)


Same plate flipped (I added a loupe so you can see the color band)


Glass cover slip cabins don’t do shit


Once it’s on a plate, the whole culture is infected.  I made the mistake of putting multiple cultures on a single plate to try and save plates and ended up infecting my entire culture stock before I knew what I was dealing with

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Awfullotofshrooms]
    #29589278 -

Idk bro, shit don't look right to me.

I'm not the right guy to talk to about that. Maybe someone else can help

Sorry man 😔


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Re: AGAR ENVY! (Anything and All things agar!) [Re: Archespore]
    #29589586 -

perhaps ur right fahtster about the estero and bisporus but I dont see anything on my ttbvi plates they look pretty clean


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Re: AGAR ENVY! (Anything and All things agar!) [Re: Anomalocaris]
    #29589604 -

By no means am I saying to not see em through.  Tried to convey that it’s worth it to run em, especially if they’re bvi or any other aggressive var.  more of a word of warning to keep an eye out for it.  If your trays don’t work out, that’s probably why.. or fruit poorly on the first flush, just pull whatever they do and rehydrate.. there’s a good chance things will improve.

What’s giving me pause about a lot of your plates is the lack of surface myc on the first grouping and the myc looks stressed on the blue plates.  I hope I’m wrong.. like I said, grain of salt and just a heads up

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Re: AGAR ENVY! (Anything and All things agar!) [Re: fahtster]
    #29589671 -

But what about that one



It looks perfect to me


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Re: AGAR ENVY! (Anything and All things agar!) [Re: Tormato]
    #29589826 -

Here's some pictures from my plates in the SAB. I know one is obviously pretty tam'd up but I want some hot takes on others. Thoughts on if they're clean or not?













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Take me back to November
Hawaiian shirts in the winter, deep thoughts, deep thoughts
Naw, take me back to November, wassup

Edited by Doctor_Doggo (05/29/26 06:40 PM)

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Doctor_Doggo] * 1
    #29589835 -



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REPENT

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Doctor_Doggo]
    #29589843 -

Doctor_Doggo said:




Id try tranferring atiny piece from the whitest part of the far right ring, to me it looks to be the cleanest part out of all the "plates". Look up the Biopsy Method by Josex


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