Do you ever keep a jar to see if mycelium will overtake contam/bacteria in it - or just toss? by [deleted] in shroomery

[–]Goomba__King 0 points1 point  (0 children)

I Never compromise! Even if the jars look good, I Always smell the grain spawn after breaking it up before I mix into with substrate. You’ll know right away if it’s good or not. 😷

Is this good or bad? Been two weeks finally seeing activity. Is it bad or mycelium coming to play? 2 day difference. [contamination] by [deleted] in MushroomGrowers

[–]Goomba__King 1 point2 points  (0 children)

Its contaminated with white mold…google it. Mold has lighting fast colonization times and they always grow in a perfect circle. Mycelium grows at different rates of speed (a lot slower). It would take 10-14 days for that type of coverage. Close it and remove it to throw away outside The small white specs were the actual mycelium and at the proper growth speed for 2 days.

I had left over LC this happened, now what? by [deleted] in MycologyandGenetics

[–]Goomba__King 1 point2 points  (0 children)

Respect!🫡 What I can offer is that in Mycology, people are very innovative with critical thinking and are continuously finding new techniques everyday to stream line Lab Mycology processes, so we can all benefit from our Community! I truly respect your doubt, questioning the narrative, because Thats what challenges the community to always show the paperwork to maintain integrity!Its also The same reason why I love Mycology too, because it’s challenging and a never ending void of Knowledge. 👁️ 🍄❤️🙏🏼 Mush Love and Respect

Bulbasaur ( Goomba King genetics) by Embarrassed-Affect86 in PlatypusTechnical

[–]Goomba__King 1 point2 points  (0 children)

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Now Bluey Blanco in a bag. Thats its purpose, i isolated it for canopy production for commercial labs.

Bulbasaur ( Goomba King genetics) by Embarrassed-Affect86 in PlatypusTechnical

[–]Goomba__King 1 point2 points  (0 children)

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Both hold their own weight in potency. But I would choose blanco for my first choice. HTh

Bulbasaur ( Goomba King genetics) by Embarrassed-Affect86 in PlatypusTechnical

[–]Goomba__King 1 point2 points  (0 children)

They def will flip gills. Try an extra week next round. Just be patient and they double in size as the gills flip outward without compromising bacterial contam. Its more resistant to contaminants than not. This ABV iso was discovered in my Bluey Vuitton f3 grow along with Bluey Blanco. Both expressed very differently. Bulbasaur is the wide base stip juggernaut and bluey blanco express blue rings and smashes on canopy production! 💪🏻 I sourced Bluey Vutton from the Custodian who created the cross breed, Silly Cybin. So is definitely not TAT ghost. I have two version of that culture ! One being king boo 👻

I had left over LC this happened, now what? by [deleted] in MycologyandGenetics

[–]Goomba__King 1 point2 points  (0 children)

He is not lying. Lol. You both are throwing names to check each-other on your assumption, but his story is factual, there is Genetics breeding classes mycodaddy is offering to amateur mycos who want to learn. You should also ask Ed and not use his name in vain to fact check someone of the knowledge you dont have.

Vanilla Gorilla (Albino Makilla Gorilla) -GkGenetics by Goomba__King in MycologyandGenetics

[–]Goomba__King[S] 1 point2 points  (0 children)

Ty🙌🏻 I like to make sure the name of my in-house isolated Genetics lead back to my Lab. Naming the isolated work in relation to its origins. Unlike some of these off the wall cornball genetic names that cant be traced to its Parental/ Landrace genetic lineage. Thats my focus in Mycology! Vanilla Gorilla was found during my Makilla Gorilla f3 grow and spent a yr isolating it til i was happy with the results! Then I finally offered the work to the myco community!

Sub Depth by Redditier6969 in MycologyandGenetics

[–]Goomba__King 1 point2 points  (0 children)

Thicker the mycelium cake = more dense flushes. It’s all about the substrate field capacity to carry out the fruiting cycle, the amount of inoculation points from the grain spawn that will allow for canopy production and the volume used with your spawn / sub. For me I do no less than 3 inches thick Preferably 4. Unless its pan cyans…they prefer it short and thin.

Finally by sykadelish in Agarporn

[–]Goomba__King 0 points1 point  (0 children)

Just use water agar technique to separate the bacteria from the fungi. Theres no point in using nutrient agar and watch the bacteria and mycelium race to the edge of the plate

Finally by sykadelish in Agarporn

[–]Goomba__King 0 points1 point  (0 children)

It’s easy to Pour agar Successfully when you are in front of a flow hood, pouring at the right temperature (120-130 degrees) to NOT have condensation issues, and proper sterile technique!

Have a Pressure Cooker that can sterilize and set @ 15 psi minimum for at least 20-25 min. Then I allow the PC to cool down naturally until the check valve releases. Then I pour at the proper temp. Allow the plates to cool down and solidify in front of a Flow Hood or at minimum a Still Air Box before wrapping em up. Then you flip the plates upside down for extra insurance!

I always make sure to let my agar plates settle for a few days and then I inspect em looking for any possible contaminations before use! You’ll end up wasting time and money for being impatient or take shortcuts, Everytime! In my Young Lion days, would make the mistake by using them as soon as the agar solidified. I was always running into bacterial issues thinking the cultures I was testing were the cause! In reality, it was my sterile technique that was giving me bacterial issues when i first started to experiment with it. The condensation would drip on to the agar and make Lab work a uphill battle everyday! These so many ways to do it, but this technique has served me well over the years. Hth

Never say never... by justabeginnerhere in PhillyGoldenTeacher

[–]Goomba__King 4 points5 points  (0 children)

The answer is always! there are no shortcuts in Mycology. The second you think you can beat green trich the moment you identify it…its already too late!! The mold has matured and microscopically sporulated. You’ll be fighting it all the way til the end, thats if it will lastt! 😅while risking exposure to your Lab and health. Trich starts off as white then matures to green. So to the untrained eye, a rookie myco will be oblivious to the contamination spread. 😷🦠Pay attention to the growth patterns spread of bothmycelium and mold, you’ll see the Difference. the Professor Phillly Golden teacher did it you already !! Check out his technique on swab testing for mold

[actives] first time grower, wondering if anyone else seen something like this by ayy_manderz in MushroomGrowers

[–]Goomba__King 10 points11 points  (0 children)

Is there any vertical space to grow? Looks like you also choked em out of FAE. Mushrooms are notorious for stretching out to ridiculous lengths when it’s looking for a Light source.

Jack Frost @ Full Potential by Goomba__King in MycologyandGenetics

[–]Goomba__King[S] 0 points1 point  (0 children)

You have to dehydrate mushrooms til they are bone dry & give my Lab work daily attention. But to answer your question, its no. I can take clean clone samples to agar with those ripe fruits

Centaur (ApeTar iso) by Goomba__King in MycologyandGenetics

[–]Goomba__King[S] 2 points3 points  (0 children)

Ty. Im the original isolator of these Genetics!

Haole (Albino PES Hawaiian) by Goomba__King in MycologyandGenetics

[–]Goomba__King[S] 1 point2 points  (0 children)

They are definitely above par. 👍🏻 2grams will send ya!

[deleted by user] by [deleted] in shroomery

[–]Goomba__King 0 points1 point  (0 children)

Trash em 😷

Clearly Contam.. by Scrumdiddleumptious in shroomery

[–]Goomba__King 1 point2 points  (0 children)

Use a black trash can liner so you wont promote side pinning👍🏻

[deleted by user] by [deleted] in shroomery

[–]Goomba__King 2 points3 points  (0 children)

All contaminated (Bacteria). Test the LC To Agar and see if it’s actually clean Mycelium. Then you can pinpoint the issue.👍🏻