questions about plant steroids

gms585

Member
so I've done some searching here and with google and I'm not finding the info I'm looking for specifically. let me break it down:
1) are there plant steroids like testosterone and hgh for humans and other mammals?
2) if there are steroids like this for plants what are they and are they usable on cannabis?
 

gms585

Member
Yea they are called Nutrients and they sell em everywhere
idk if you just don't understand the question or you just have limited knowledge yourself. nutrients for plants are basically potassium phosphorus and nitrogen just like for a mammal they are protein fat and carbohydrate. hormones like testosterone or hgh cause a mammal to synthesis those nutrients at a superior frequency resulting in faster and sometimes stronger growth. i am asking if science has isolated the hormones that cause a plants to synthesis nutrients faster. if you don't know what I'm even talking about why answer?
 

Becorath

Well-Known Member
no problem. it is sold at most any garden supply. It has tons of stuff and a little goes a long way. it helps with most any stage of growing.
 

DRHBONES

Member
YEAHMAN !
Biologists learn how plants synthesize their growth hormone auxin

October 24, 2011 Biologists at the University of California, San Diego have succeeded in unraveling, for the first time, the complete chain of biochemical reactions that controls the synthesis of auxin, the hormone that regulates nearly all aspects of plant growth and development.


Their discovery, detailed in a paper in this week's online edition of the Proceedings of the National Academy of Sciences, will allow agricultural scientists to develop new ways to enhance or manipulate auxin production to improve the growth and yield of crops and other plants.
More than a century ago, Charles Darwin noticed that plants produced a substance that made them bend toward light, a hormone called auxin that biologists have since found to be essential not only in regulating plant growth but also in patterning their development.
In 2006, a team of San Diego researchers headed by Yunde Zhao, an associate professor of biology at UC San Diego, discovered a family of 11 genes involved in the synthesis of auxin. Building on that work, Zhao and his colleagues at UCSD, the Salk Institute for Biological Studies and RIKEN, Japan's natural sciences research institute, have now unraveled the main biochemical pathway leading to the synthesis of auxin.
"How plants synthesize this important hormone had remained a mystery for almost a century," said Zhao. "Several genes had been known to play important roles in auxin biosynthesis in plants, but the information was fragmented and no complete auxin biosynthesis pathways in plants were identified.'
In their study, Zhao and his colleagues used sophisticated genetic approaches in combination with analytical biochemistry to identify a simple two-step chain of biochemical reactions in the genetic model plant Arabidopsis that converts tryptophan to indole-3-acetic acid, the main auxin hormone synthesized in plants.
"The main reason that auxin biosynthesis mechanisms had evaded scientists is that each step in auxin biosynthesis involves many genes, making the genetic dissection of auxin biosynthesis very complicated," said Zhao. "Now that we've identified the main auxin biosynthesis pathway in plants, we will be able to regulate auxin levels in crops and other plants with temporal and spatial precision, providing useful tools for agricultural biotechnology."
"Auxin affects virtually every aspect of plant growth, including most traits that are important for agriculture," said Mark Estelle, a professor of biology at UC San Diego and one of the world's experts on auxin. "For example, auxin regulates plant stature, the number and shape of plant organs, as well as seed and fruit development."
"This discovery has many important implications," he added. "To the basic scientist, knowledge of auxin synthesis will aid in the understanding of many fundamental aspects of plant development. To the farmer, this advance will open up many new opportunities for crop improvement. This is particularly important as our society faces the daunting challenges of a growing global population and a changing climate."

Provided by University of California - San Diego (news : web)
 

DRHBONES

Member
Indole-3-acetic acid, also known as IAA, is a heterocyclic compound that is a phytohormone called auxin. This colourless solid is native plant compound, potent and the most important auxin.[1] The molecule is derived from indole, containing a carboxymethyl group (acetic acid).
Biosynthesis and biological activity
Main article: Auxin
IAA is predominantly produced in cells of the apex (bud) and very young leaves of a plant. Plants can synthesize IAA by several independent biosynthetic pathways, four of them starts from tryptophan, but there is also biosynthetic pathway independent of tryptophan.[2] Plants mainly produce IAA from tryptophan through indole-3-pyruvic acid.[3][4] IAA is also produced from tryptophan through indole-3-acetaldoxime in Arabidopsis.[5]
IAA has many different effects, as all auxins do, such as inducing cell elongation and cell division with all subsequent results for plant growth and development. On larger scale, IAA serves as signaling molecule necessary for development of plant organs and coordination of growth.
There are less expensive and metabolically stable synthetic auxin analogs on the market for use in horticulture, such as indole-3-butyric acid (IBA) and 1-naphthaleneacetic acid (NAA).[citation needed]
Studies of IAA in the 1940s led to the development of the phenoxy herbicides 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). Like IBA and NAA, 2,4-D and 2,4,5-T are metabolically and environmentally more stable analogs of IAA. However, when sprayed on broad-leaf dicot plants, they induce rapid, uncontrolled growth, eventually killing them. First introduced in 1946, these herbicides were in widespread use in agriculture by the middle of the 1950s.
Synthesis
Chemically, it can be synthesized by the reaction of indole with glycolic acid in the presence of base at 250

 
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