What are brassinosteroids?

What are brassinosteroids?

Brassinosteroids (BRs) are a group of steroid hormones, essentially important for plant development and growth. BR signaling functions to promote cell expansion and cell division, and plays a role in etiolation and reproduction.

How do brassinosteroids work?

Brassinosteroids (BRs) as a class of steroid plant hormones participate in the regulation of numerous developmental processes, including root and shoot growth, vascular differentiation, fertility, flowering, and seed germination, as well as in responding to environmental stresses.

What is the precursor of brassinosteroids?

Many of the known BRs are biosynthetic precursors or metabolic products of BL, although castasterone, the immediate precursor of BL, is believed to have independent biological activity in some plants.

What are brassinosteroids synthesized from?

An array of brassinosteroids with variations in C-24 alkyl substituents are synthesized from campesterol, sitosterol, and cholesterol.

Which plants contain brassinosteroids?

Brassinosteroids have been found in various species of plants, including monoplast freshwater algae and brown algae, indicating that BRs are a widespread ancient plant hormone [11].

Where are Brassinosteroids found in plants?

Brassinosteroids have been found in various species of plants, including monoplast freshwater algae and brown algae, indicating that BRs are a widespread ancient plant hormone [11]. Distributions of BRs differ among distinct tissues of individual species.

What is the function of jasmonic acid in plants?

The major function of JA and its various metabolites is regulating plant responses to abiotic and biotic stresses as well as plant growth and development. Regulated plant growth and development processes include growth inhibition, senescence, tendril coiling, flower development and leaf abscission.

What is jasmonic acid significance?

Jasmonic acid (JA) is an endogenous growth-regulating substance, initially identified as a stress-related hormone in higher plants. Similarly, the exogenous application of JA also has a regulatory effect on plants. Abiotic stress often causes large-scale plant damage.

How is jasmonic acid produced?

Biosynthesis. Its biosynthesis starts from the fatty acid linolenic acid, which is oxygenated by lipoxygenase (13-LOX), forming a hydroperoxide. This peroxide then cyclizes in the presence of allene oxide synthase to form an allene oxide.

What is the pH of jasmonic acid?

The solubility of (±)-jasmonic acid in PBS, pH 7.2, is approximately 3 mg/ml. We do not recommend storing the aqueous solution for more than one day. 1. Creelman, R.A. and Mullet, J.E.

What is the function of jasmonic acid?

What is the role of jasmonic acid?

What do we know about the hormonal status of brassinosteroids?

reviews The structure, biosynthesis and function of brassinosteroids o.oo o.o,o The hormonal status of brassinosteroids has been established by coupling molecular genetics with studies of the pathway of biosynthesis.

How are brassinosteroids biosynthesized?

Brassinosteroids are biosynthesized from a C28plant sterol called campesterol by a reductive step followed by several oxidative steps (Fig. 17.34). The biosynthesis of brassinolide from campesterol requires app. 12 steps. The reductive step and one of the several oxidative steps are catalysed by enzymes DET2 and CPD respectively.

What are the vicinal hydroxyls of brassinosteroids?

In the side chain, brassinosteroids have a-oriented vicinal hydroxyls at positions C22 and C23 (in the side chain stereochemistry of steroids, groups in front of the plane are defined as a-orientedT). Cathasterone, with a single hydroxyl at C22, is a precursor ofbrassinosteroids with a 22,23-vicinal diol.

How do brassinosteroids regulate gene expression in plant cells?

Expression of a plant gene with sequence similarity to animal TGF-beta receptor interacting protein is regulated by brassinosteroids and required for normal plant development. Plant J.2635–45. [PubMed] [Google Scholar] Jinn, T.L., Stone, J.M., and Walker, J.C. (2000).

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