|Artificial cocaine biosynthesis||Bookmark|
The thread containing the post Post 295864 (Organikum: "Biosomething", Novel Discourse) talks about possibily adapting this method for producing ephedra to produce cocaine. Has anyone made any progress researching this option?
I'm afraid I don't know too much about microbiology (but can certainly learn), but I will likely soon have access to a quantity of erythroxylum coca plants, and would be happy to give culturing cocaine in a tub a shot if I had some pointers on what the procedure would look like.
* Is everyone agreed that this is at least a reasonable possibility, biologically speaking?
* Would it be completely impossible to do without industrial facilities?
* Has anyone found a translation of the patent discussed Post 295864 (Organikum: "Biosomething", Novel Discourse) here?
* Is there a particular area of biology that would focus on this topic?
I'm certainly not opposed to putting a fair bit of effort into this, as long as there's a reasonable chance of success.
|ephedra cell ZHJ-25 CGMCC No.0359||Bookmark|
The patent in Organikum's post refers to "ephedra cell ZHJ-25 CGMCC No.0359". Here's the patent on it:
Title: Ephedra cell ZHJ-25 CGMCC No.0359 and its induction method
Application Number: 98125187 Application Date: 1998.12.04
Publication Number: 1256309 Publication Date: 2000.06.14
Approval Pub. Date: Granted Pub. Date:
International Classification: C12N 5/04
Applicant(s) Name: Inst. of Chemical Metallurgy, Chinese Academy of Sciences
Inventor(s) Name: Cha Lihang
Attorney & Agent: gao cunxiu
The present invention relates to the utilization of biological technology. The induced Ephedra cell ZHJ-25 is preserved in Chinese Microbe Preservation Center in the code of CGMCC No.0359. The induction method of the present invention is t hat after cleaning and disinfection, Ephedra plant is inoculated into culture medium with 1.0-10% wt./vol.sugar culture medium for culture at 23-26 deg.c for 5-30 days to obtain Ephedra callus, which is then transferred to culture medium fo r subculture. The Ephedra cell of the present invention has a proliferation of 3-5 times and a ephedrine content of 0.1-20% dry weight.
|omg the possibilities||Bookmark|
perhaps this could also be adapted to other plants too - for example, peyote, mimosa hostilis, iboga... hmmm perhaps that acacia rididula or berklandii (sp?)... certainly the possibility of vat culturing fungi has been well researched and usable now.
dammit now I am really going to have to learn tissue culturing and progress from there...
we can't stop here, this is bat country