BLASTICIDIN S Chemical Properties

Melting point:

235°C

Boiling point:

539.06°C (rough estimate)

alpha 

D11 +108.4° (water)

Density 

1.1690 (rough estimate)

vapor pressure 

Low

refractive index 

1.6910 (estimate)

solubility 

DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble; Water: soluble

form 

A solid

pka

2.4 (carboxyl), 4.6,8.0 and>12.5 (three bases)

Water Solubility 

>30 g l^-1(20 °C)

Stability:

Incompatible with strong oxidizing agents.

EPA Substance Registry System

Blasticidin S (2079-00-7)

Safety Information

Hazard Codes 

T+

Risk Statements 

28

Safety Statements 

24/25-36/37-45

RIDADR 

3172

HazardClass 

6.1(a)

PackingGroup 

II

HS Code 

29349990

Hazardous Substances Data

2079-00-7(Hazardous Substances Data)

Toxicity

LD50 i.v. in mice: 2.82 mg/kg (Takeuchi)

BLASTICIDIN S Usage And Synthesis

Description

Nucleoside antibiotic produced by Streptomyces griseochromogenes (1). Biosynthesized from cytosine, glucose, arginine, and methionine (2).

Uses

Blasticidin S is a nucleoside produced by several species of Streptomyces, first reported in the late 1950s. Blasticidin S is an antifungal agent with particularly potent activity against the rice pathogen, Piricularia oryzae, for which it was used commercially for some time in Japan. Blasticidin S inhibits protein synthesis and is active against bacteria, tumour cell lines and nematodes. More recently, blasticidin S has been used as a marker for strain manipulations. Blasticidin S provided by BioAustralis is presented as the free base to avoid problems associated with the use of the hydrochloride.

Uses

Blasticidin-S is used for the control of rice blast (PyricuZuria oryzae) by foliar application.

Definition

ChEBI: A blasticidin that is an antibiotic obtained from Streptomyces griseochromogene.

Production Methods

Blasticidin S is produced by Streptomyces griseochromogenes, and has a wide range of antimicrobial activity (4). This antibiotic was utilized in the Far East beginning in 1961 against the rice blast pathogen Pyricularia oryzae, with effective control achieved at rates of 10–40 ppm (4).

General Description

Blasticidin S was found in the culture broth of Streptomyces griseochromogenes by Yonehara et al. of the University of Tokyo in 1958. It has a nucleoside-analogue structure and shows strong activity against phytopathogenic fungi, especially Pericularia oryzae, the pathogen causing rice blast. Blasticidin S has been used to protect rice plants.

Pharmacology

Inhibits protein synthesis both in eukaryotes and in prokaryotes (5,6). Interacts with ribosomal RNA in large subunit, interfering with the transpeptidation step. Inhibits cell-free protein synthesis in P. oryzae and Escherichia coli.

Metabolic pathway

Several blasticidin S-resistant microorganisms are found to produce blasticidin S deaminase which catalyzes the hydrolytic deamination of the cytosine moiety in blasticidin S to give a non-toxic deaminohydroxy derivative.

Metabolism

3H-blasticidin S administered to mice was excreted in the urine and feces within 24 h. Cytomycin and cytosin were identified as the main metabolites in and on rice plants, respectively (7). In soil, DT₅₀ < 5 d. Metabolized to nontoxic deaminohydroxy blasticidin S by Aspergillus sp. and resistant Bacillus cereus. Novel deaminase and coding genes, BSD and bsr, were isolated as selectable marker genes for genetic engineering (8).

Toxicity evaluation

Acute oral LD₅₀ for male rats: 56.8, female rats: 55.9, male mice: 51.9, and female mice: 60.1 mg/kg. Acute percutaneous LD₅₀ for rats >500 mg/kg. Eye: severe irritation.

Degradation

Blasticidin-S is obtained as white needle crystals which are very soluble in water. The compound is stable in the pH range 5-7 but it is unstable under alkaline conditions. It is readily degraded by sunlight when on the surface of rice plants with the main degradation product being cytosine (2) (Yamaguchi et al., 1972) as shown in Scheme 1.

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