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Muricarpone B

$1,120

  • Brand : BIOFRON

  • Catalogue Number : BN-O0915

  • Specification : 98%(HPLC)

  • CAS number : 886226-15-9

  • Formula : C19H22O5

  • Molecular Weight : 330.37

  • PUBCHEM ID : 11573476

  • Volume : 5mg

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Catalogue Number

BN-O0915

Analysis Method

HPLC,NMR,MS

Specification

98%(HPLC)

Storage

2-8°C

Molecular Weight

330.37

Appearance

Oil

Botanical Source

Structure Type

Phenols

Category

Standards;Natural Pytochemical;API

SMILES

C1=CC(=C(C=C1CCCCC(=O)CCC2=CC(=C(C=C2)O)O)O)O

Synonyms

3-Heptanone, 1,7-bis(3,4-dihydroxyphenyl)-/1,7-Bis(3,4-dihydroxyphenyl)-3-heptanone

IUPAC Name

1,7-bis(3,4-dihydroxyphenyl)heptan-3-one

Density

1.3±0.1 g/cm3

Solubility

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

Flash Point

339.8±28.0 °C

Boiling Point

615.1±55.0 °C at 760 mmHg

Melting Point

InChl

InChI=1S/C19H22O5/c20-15(8-5-14-7-10-17(22)19(24)12-14)4-2-1-3-13-6-9-16(21)18(23)11-13/h6-7,9-12,21-24H,1-5,8H2

InChl Key

UHRUXUCWHIGENP-UHFFFAOYSA-N

WGK Germany

RID/ADR

HS Code Reference

2933990000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:886226-15-9) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

32050898

Abstract

Background
Cotton Verticillium wilt is one of the most devastating diseases for cotton production in the world. Although this diseases have been widely studied at the molecular level from pathogens, the molecular basis of V. dahliae interacted with cotton has not been well examined.

Results
In this study, RNA-seq analysis was carried out on V. dahliae samples cultured by different root exudates from three cotton cultivars (a susceptible upland cotton cultivar, a tolerant upland cotton cultivar and a resistant island cotton cultivar) and water for 0 h, 6 h, 12 h, 24 h and 48 h. Statistical analysis of differentially expressed genes revealed that V. dahliae responded to all kinds of root exudates but more strongly to susceptible cultivar than to tolerant and resistant cultivars. Go analysis indicated that ‘hydrolase activity, hydrolyzing O-glycosyl compounds’ related genes were highly enriched in V. dahliae cultured by root exudates from susceptible cotton at early stage of interaction, suggesting genes related to this term were closely related to the pathogenicity of V. dahliae. Additionally, ‘transmembrane transport’, ‘coenzyme binding’, ‘NADP binding’, ‘cofactor binding’, ‘oxidoreductase activity’, ‘flavin adenine dinucleotide binding’, ‘extracellular region’ were commonly enriched in V. dahliae cultured by all kinds of root exudates at early stage of interaction (6 h and 12 h), suggesting that genes related to these terms were required for the initial steps of the roots infections.

Conclusions
Based on the GO analysis results, the early stage of interaction (6 h and 12 h) were considered as the critical stage of V. dahliae-cotton interaction. Comparative transcriptomic analysis detected that 31 candidate genes response to root exudates from cotton cultivars with different level of V. dahliae resistance, 68 response to only susceptible cotton cultivar, and 26 genes required for development of V. dahliae. Collectively, these expression data have advanced our understanding of key molecular events in the V. dahliae interacted with cotton, and provided a framework for further functional studies of candidate genes to develop better control strategies for the cotton wilt disease.

KEYWORDS

Root exudates, Transcriptome, Verticillium dahliae, Hydrolase activity, hydrolyzing O-glycosyl compounds hydrolase

Title

Transcriptomic analysis of gene expression of Verticillium dahliae upon treatment of the cotton root exudates

Author

Xinyu Zhang,1 Wenhan Cheng,1 Zhidi Feng,1 Qianhao Zhu,2 Yuqiang Sun,3 Yanjun Li,corresponding author1 and Jie Suncorresponding author1

Publish date

2020;


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