Science | Nature | Cell | View More
Natural Products
Streptolydigin
Streptolydigin
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Streptolydigin
Price:
CAS No.: 7229-50-7
Catalog No.: CFN00138
Molecular Formula: C32H44N2O9
Molecular Weight: 600.7 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: From Streptomyces lydicus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
Guestbook:
Contact Us
Order & Inquiry & Tech Support

Tel: (0086)-27-84237683
Tech: service@chemfaces.com
Order: manager@chemfaces.com
Address: 176, CheCheng Eest Rd., WETDZ, Wuhan, Hubei 430056, PRC
How to Order
Orders via your E-mail:

1. Product number / Name / CAS No.
2. Delivery address
3. Ordering/billing address
4. Contact information
Order: manager@chemfaces.com
Delivery time
Delivery & Payment method

1. Usually delivery time: Next day delivery by 9:00 a.m. Order now

2. We accept: Wire transfer & Credit card & Paypal
Citing Use of our Products
* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
Our products had been exported to the following research institutions and universities, And still growing.
  • National Hellenic Research Foun... (Greece)
  • Universitas islam negeri Jakarta (Indonesia)
  • University of East Anglia (United Kingdom)
  • Kyushu University (Japan)
  • University of Leipzig (Germany)
  • University of Vienna (Austria)
  • Universidade Federal de Pernamb... (Brazil)
  • Worcester Polytechnic Institute (USA)
  • Auburn University (USA)
  • Shanghai University of TCM (China)
  • Deutsches Krebsforschungszentrum (Germany)
  • More...
Package
Featured Products
Soyasaponin Bb

Catalog No: CFN90456
CAS No: 51330-27-9
Price: $138/20mg
Dehydroglyasperin C

Catalog No: CFN96483
CAS No: 199331-35-6
Price: $ / mg
Colchicine

Catalog No: CFN99514
CAS No: 64-86-8
Price: $40/20mg
Campesterol

Catalog No: CFN92204
CAS No: 474-62-4
Price: $188/10mg
Gentisic acid

Catalog No: CFN92451
CAS No: 490-79-9
Price: $40/20mg
Saikosaponin D

Catalog No: CFN99989
CAS No: 20874-52-6
Price: $40/20mg
Mulberrin

Catalog No: CFN97085
CAS No: 62949-79-5
Price: $288/20mg
Monomethyl lithospermate

Catalog No: CFN91005
CAS No: 933054-33-2
Price: $333/10mg
1-Dehydro-10-gingerdione

Catalog No: CFN92374
CAS No: 136826-50-1
Price: $ / mg
Trans-Ferulic acid

Catalog No: CFN92394
CAS No: 537-98-4
Price: $30/20mg
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Streptolydigin has antibacterial activity against a number of Gram positive bacteria. It inhibits RNA polymerase by sequestering the active center in a catalytically inactive conformation.
Targets: Antifection | NADPH-oxidase | DNA/RNA Synthesis
In vitro:
Antimicrob Agents Chemother. 2014;58(3):1420-4.
Antibiotic streptolydigin requires noncatalytic Mg2+ for binding to RNA polymerase.[Pubmed: 24342645]
Multisubunit RNA polymerase, an enzyme that accomplishes transcription in all living organisms, is a potent target for antibiotics. The antibiotic Streptolydigin inhibits RNA polymerase by sequestering the active center in a catalytically inactive conformation.
METHODS AND RESULTS:
Here, we show that binding of Streptolydigin to RNA polymerase strictly depends on a noncatalytic magnesium ion which is likely chelated by the aspartate of the bridge helix of the active center. Substitutions of this aspartate may explain different sensitivities of bacterial RNA polymerases to Streptolydigin.
CONCLUSIONS:
These results provide the first evidence for the role of noncatalytic magnesium ions in the functioning of RNA polymerase and suggest new routes for the modification of existing and the design of new inhibitors of transcription.
J Bacteriol. 2011 Aug;193(16):4214-23.
Amino acid precursor supply in the biosynthesis of the RNA polymerase inhibitor streptolydigin by Streptomyces lydicus.[Pubmed: 21665968]
Biosynthesis of the hybrid polyketide-nonribosomal peptide antibiotic Streptolydigin, 3-methylaspartate, is utilized as precursor of the tetramic acid moiety.
METHODS AND RESULTS:
The three genes from the Streptomyces lydicus Streptolydigin gene cluster slgE1-slgE2-slgE3 are involved in 3-methylaspartate supply. SlgE3, a ferredoxin-dependent glutamate synthase, is responsible for the biosynthesis of glutamate from glutamine and 2-oxoglutarate. In addition to slgE3, housekeeping NADPH- and ferredoxin-dependent glutamate synthase genes have been identified in S. lydicus. The expression of slgE3 is increased up to 9-fold at the onset of Streptolydigin biosynthesis and later decreases to ∼2-fold over the basal level. In contrast, the expression of housekeeping glutamate synthases decreases when Streptolydigin begins to be synthesized. SlgE1 and SlgE2 are the two subunits of a glutamate mutase that would convert glutamate into 3-methylaspartate. Deletion of slgE1-slgE2 led to the production of two compounds containing a lateral side chain derived from glutamate instead of 3-methylaspartate. Expression of this glutamate mutase also reaches a peak increase of up to 5.5-fold coinciding with the onset of antibiotic production.
CONCLUSIONS:
Overexpression of either slgE3 or slgE1-slgE2 in S. lydicus led to an increase in the yield of Streptolydigin.
J Am Chem Soc. 2011 Aug 10;133(31):12172-84.
Chemical synthesis enables biochemical and antibacterial evaluation of streptolydigin antibiotics.[Pubmed: 21714556]
Inhibition of bacterial transcription represents an effective and clinically validated anti-infective chemotherapeutic strategy. We describe the evolution of our approach to the Streptolydigin class of antibiotics that target bacterial RNA polymerases (RNAPs). This effort resulted in the synthesis and biological evaluation of Streptolydigin, Streptolydiginone, streptolic acid, and a series of new Streptolydigin-based agents. Subsequent biochemical evaluation of RNAP inhibition demonstrated that the presence of both streptolic acid and tetramic acid subunits was required for activity of this class of antibiotics. In addition, we identified 10,11-dihydroStreptolydigin as a new RNAP-targeting agent, which was assembled with high synthetic efficiency of 15 steps in the longest linear sequence.
CONCLUSIONS:
DihydroStreptolydigin inhibited three representative bacterial RNAPs and displayed in vitro antibacterial activity against S. salivarius . The overall increase in synthetic efficiency combined with substantial antibacterial activity of this fully synthetic antibiotic demonstrates the power of organic synthesis in enabling design and comprehensive in vitro pharmacological evaluation of new chemical agents that target bacterial transcription.
Streptolydigin Description
Source: From Streptomyces lydicus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
ChemFaces New Products and Compounds
Tembetarine

Catalog No: CFN95542
CAS No: 18446-73-6
Price: $318/5mg
Oblongaroside B

Catalog No: CFN95543
CAS No: 1000889-11-1
Price: $318/10mg
(2S)-5,7,3',4'-tetramethoxyflavano...

Catalog No: CFN95406
CAS No: 74628-43-6
Price: $318/10mg
Genistein 7-O-beta-D-glucopyranosi...

Catalog No: CFN95159
CAS No: 70404-42-1
Price: $318/10mg
Ganoweberianic acid E

Catalog No: CFN95504
CAS No: 1309931-90-5
Price: $413/5mg
Atractylochromene

Catalog No: CFN95162
CAS No: 203443-33-8
Price: $318/10mg
Lappaol B

Catalog No: CFN95242
CAS No: 62359-60-8
Price: $333/10mg
Ganolucidic acid B

Catalog No: CFN95513
CAS No: 98683-75-1
Price: $413/5mg
Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.6647 mL 8.3236 mL 16.6472 mL 33.2945 mL 41.6181 mL
5 mM 0.3329 mL 1.6647 mL 3.3294 mL 6.6589 mL 8.3236 mL
10 mM 0.1665 mL 0.8324 mL 1.6647 mL 3.3294 mL 4.1618 mL
50 mM 0.0333 mL 0.1665 mL 0.3329 mL 0.6659 mL 0.8324 mL
100 mM 0.0166 mL 0.0832 mL 0.1665 mL 0.3329 mL 0.4162 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Kinase Assay:
J Ind Microbiol Biotechnol. 2013 Nov;40(11):1303-14.
Insights into the roles of exogenous glutamate and proline in improving streptolydigin production of Streptomyces lydicus with metabolomic analysis.[Pubmed: 23990132 ]
The addition of precursors was one strategy to improve antibiotic production. The exogenous proline and glutamate, as precursors of Streptolydigin, could significantly improve the Streptolydigin production, but their underlying molecular mechanisms remain unknown.
CONCLUSIONS:
Herein, metabolomic analysis was carried out to explore the metabolic responses of Streptomyces lydicus to the additions of proline and glutamine. The significant differences in the quantified 53 metabolites after adding the exogenous proline and glutamate were enunciated by gas chromatography coupled to time-of-flight mass spectrometry. Among them, the levels of some fatty acids (e.g., dodecanoic acid, octadecanoic acid, hexadecanoic acid) were significantly decreased after adding glutamate and proline, indicating that the inhibition of fatty acid synthesis might be benefit for the accumulation of Streptolydigin. Particularly, the dramatic changes of the identified metabolites, which are involved in glycolysis, the tricarboxylic acid cycle, and the amino acid and fatty acid metabolism, revealed that the additions of glutamate and proline possibly caused the metabolic cross-talk in S. lydicus. Additionally, the level of intracellular glutamate dramatically enhanced at 12 h after adding proline, showing that exogenous proline may be firstly convert into glutamate and consequently result in crease of the Streptolydigin production. The high levels of Streptolydigin at 12 and 24 h after adding glutamate unveiled that part glutamate were rapidly used to synthesize the Streptolydigin. Furthermore, there is the significant difference in metabolomic characteristics of S. lydicus after adding glutamate and proline, uncovering that multiple regulatory pathways are involved in responses to the additions of exogenous glutamate and proline.
CONCLUSIONS:
Taken together, exogenous glutamate and proline not only directly provided the precursors of Streptolydigin biosynthesis, but also might alter the metabolic homeostasis of S. lydicus E9 during improving the production of Streptolydigin.
Soyasaponin Bb

Catalog No: CFN90456
CAS No: 51330-27-9
Price: $138/20mg
Dehydroglyasperin C

Catalog No: CFN96483
CAS No: 199331-35-6
Price: $ / mg
Colchicine

Catalog No: CFN99514
CAS No: 64-86-8
Price: $40/20mg
Campesterol

Catalog No: CFN92204
CAS No: 474-62-4
Price: $188/10mg
Gentisic acid

Catalog No: CFN92451
CAS No: 490-79-9
Price: $40/20mg
Saikosaponin D

Catalog No: CFN99989
CAS No: 20874-52-6
Price: $40/20mg
Mulberrin

Catalog No: CFN97085
CAS No: 62949-79-5
Price: $288/20mg
Monomethyl lithospermate

Catalog No: CFN91005
CAS No: 933054-33-2
Price: $333/10mg
1-Dehydro-10-gingerdione

Catalog No: CFN92374
CAS No: 136826-50-1
Price: $ / mg
Trans-Ferulic acid

Catalog No: CFN92394
CAS No: 537-98-4
Price: $30/20mg
Tags: buy Streptolydigin | Streptolydigin supplier | purchase Streptolydigin | Streptolydigin cost | Streptolydigin manufacturer | order Streptolydigin | Streptolydigin distributor