gnome82 Posted May 19, 2014 Hiya all, So I have tried this several times now no luck, According to Stamets pleurotus can produce half thier dry weight in spore! Have attempted to print both coles and woolworths varieties with no luck, This doesn't seem to be problem for agaricus Was hoping someone could shed light on why they will not produce spore? Id imagine this is commercially desirable I do have two theories, 1- a non spore producing strain possibly gmo? this does not make sense though as it is the purpose of mushroom fruitbody to produce spore 2-low temp storage ceases spore production? Interestingly they do seem to revert vigorously back to growth mode mycelliating the paper they are supposed to be printing on! This has led to many experiments, but the rapid growth seems to stall after about a week Share this post Link to post Share on other sites
obtuse Posted May 19, 2014 I agree, clone them. when you get to fruiting, then print while their young. shop ones may have finished by the time you get them. Share this post Link to post Share on other sites
ace1928 Posted May 19, 2014 I've cloned a blue oyster from the shops that was actually a sporeless variety. A lot of important commercial strains ARE sporeless to help avoid health issues with workers. 1 Share this post Link to post Share on other sites
gnome82 Posted May 20, 2014 Am trying to clone aswell, not sure how well it's going... Think this strain might be more impatient than I am! Share this post Link to post Share on other sites
ace1928 Posted May 20, 2014 Try wrapping some plastic around the dish to limit oxygen. Might stall the pins and stop it from trying to make more. Worth a shot at least Share this post Link to post Share on other sites
Berengar Posted May 20, 2014 Premature pinning can also be a sign of too nutritious agar mixture. 3 Share this post Link to post Share on other sites
gnome82 Posted May 20, 2014 Yes agreed need to try something, the premature pinning must be using energy better put towards mycelial growth at this stage will try couple layers of clingwrap hopefully enough have read 10 micrometer garbage bags are permeable enough to allow gas exchange Am using h2o2 in agar, will this be a source of excess oxygen? the mycelium must need some o2 though The agar mix was 12gm malt and 5gm sawdust 1gm yeast and powered milk per Litre now I could be wrong but I thought this was on the lighter side of recommended nutrient, just trying to eliminate possible causes Share this post Link to post Share on other sites
worowa Posted May 20, 2014 Yes agreed need to try something, the premature pinning must be using energy better put towards mycelial growth at this stage will try couple layers of clingwrap hopefully enough have read 10 micrometer garbage bags are permeable enough to allow gas exchange Am using h2o2 in agar, will this be a source of excess oxygen? the mycelium must need some o2 though The agar mix was 12gm malt and 5gm sawdust 1gm yeast and powered milk per Litre now I could be wrong but I thought this was on the lighter side of recommended nutrient, just trying to eliminate possible causes Spores don't like h2o2... 2 Share this post Link to post Share on other sites
ace1928 Posted May 21, 2014 Spores don't like h2o2... That is putting it nicely Share this post Link to post Share on other sites
fungi1963 Posted May 23, 2014 H2O2 is only for clean up work or running mycelium of already germinated spores. You use it to prevent spores from germinating, hence good for high contam or low-sterile environments. Good for wild cloning too where you can dip the harvested fragment of mycelium into H2O2 to clean up the cut surfaces prior to applying to agar plates. Share this post Link to post Share on other sites
gnome82 Posted June 1, 2014 well there was just no stopping these pins 2 layers of clingwrap wasnt enough to slow growth, not havin a go ace, just reporting progress fortunatley there was also mycelial gowth aswell as pinning, which on first transfer appears to be continuing to grow without pinning now I could be wrong but I thought this was on the lighter side of recommended nutrient,just trying to eliminate possible causes appologies if this came across as pretentious, my comunication skills are poor at the best of times there probably should have been a question mark in there or something as i was trying to check wether the agar mix was too nutritious or not anywayz, am loving H202 agar, no more f*#kn glooveboxes! for the first time i do not resent the awquardness of agar work, but obviously this will make starting from spore somewhat challenging Share this post Link to post Share on other sites