Bassianolide
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Category | Antibiotics |
Catalog number | BBF-04217 |
CAS | 64763-82-2 |
Molecular Weight | 909.20 |
Molecular Formula | C48H84N4O12 |
Purity | >95% by HPLC |
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Description
It is a cyclooctadepsipeptide antibiotic isolated from the entomopathogenic fungi. It is one of the active components of beauveria bassiana biocontrol products. It has insecticidal properties.
Specification
Synonyms | (-)-Bassianolide; NSC 321804; BASS; cyclo[N(Me)Leu-D-OVal-N(Me)Leu-D-OVal-N(Me)Leu-D-OVal-N(Me)Leu-D-OVal]; cyclo[N-methyl-L-leucyl-N-oxa-D-valyl-N-methyl-L-leucyl-N-oxa-D-valyl-N-methyl-L-leucyl-N-oxa-D-valyl-N-methyl-L-leucyl-N-oxa-D-valyl] |
Storage | Store at -20°C |
IUPAC Name | (3S,6R,9S,12R,15S,18R,21S,24R)-4,10,16,22-tetramethyl-3,9,15,21-tetrakis(2-methylpropyl)-6,12,18,24-tetra(propan-2-yl)-1,7,13,19-tetraoxa-4,10,16,22-tetrazacyclotetracosane-2,5,8,11,14,17,20,23-octone |
Canonical SMILES | CC(C)CC1C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N1C)C(C)C)CC(C)C)C)C(C)C)CC(C)C)C)C(C)C)CC(C)C)C)C(C)C |
InChI | InChI=1S/C48H84N4O12/c1-25(2)21-33-45(57)61-38(30(11)12)42(54)50(18)35(23-27(5)6)47(59)63-40(32(15)16)44(56)52(20)36(24-28(7)8)48(60)64-39(31(13)14)43(55)51(19)34(22-26(3)4)46(58)62-37(29(9)10)41(53)49(33)17/h25-40H,21-24H2,1-20H3/t33-,34-,35-,36-,37+,38+,39+,40+/m0/s1 |
InChI Key | QVZZPLDJERFENQ-NKTUOASPSA-N |
Source | Beauveria bassiana |
Properties
Appearance | White Solid |
Antibiotic Activity Spectrum | Parasites |
Boiling Point | 1015.6±65.0°C (Predicted) |
Density | 1.012±0.06 g/cm3 (Predicted) |
Solubility | Soluble in Chloroform |
Reference Reading
1. The Toxins of Beauveria bassiana and the Strategies to Improve Their Virulence to Insects
Hui Peng, Peng Cheng, Wenjuan Li, Haiyang Wang, Maoqing Gong Front Microbiol . 2021 Aug 26;12:705343. doi: 10.3389/fmicb.2021.705343.
The long-term and excessive usage of pesticides is an enormous burden on the environment, which also increases pest resistance. To overcome this problem, research and application of entomopathogenic fungi, which are both environmentally friendly and cause lower resistance, have gained great momentum. Entomopathogenic fungi have a wide range of prospects. Apart fromBacillus thuringiensis,Beauveria bassianais the most studied biopesticide. After invading insect hosts,B. bassianaproduces a variety of toxins, which are secondary metabolites such as beauvericin, bassianin, bassianolide, beauverolides, tenellin, oosporein, and oxalic acid. These toxins helpB. bassianato parasitize and kill the hosts. This review unequivocally considers beauveria toxins highly promising and summarizes their attack mechanism(s) on the host insect immune system. Genetic engineering strategies to improve toxin principles, genes, or virulent molecules ofB. bassianahave also been discussed. Lastly, we discuss the future perspective ofBeauveriatoxin research, including newly discovered toxins.
2. Biosynthesis of the cyclooligomer depsipeptide bassianolide, an insecticidal virulence factor of Beauveria bassiana
Patricia Espinosa-Artiles, A A Leslie Gunatilaka, S Patricia Stock, E M Kithsiri Wijeratne, Rousel Orozco, István Molnár, Yuquan Xu Fungal Genet Biol . 2009 May;46(5):353-64. doi: 10.1016/j.fgb.2009.03.001.
Beauveria bassiana is a facultative entomopathogen with an extremely broad host range that is used as a commercial biopesticide for the control of insects of agricultural, veterinary and medical significance. B. bassiana produces bassianolide, a cyclooligomer depsipeptide secondary metabolite. We have cloned the bbBsls gene of B. bassiana encoding a nonribosomal peptide synthetase (NRPS). Targeted inactivation of the B. bassiana genomic copy of bbBsls abolished bassianolide production, but did not affect the biosynthesis of beauvericin, another cyclodepsipeptide produced by the strain. Comparative sequence analysis of the BbBSLS bassianolide synthetase revealed enzymatic domains for the iterative synthesis of an enzyme-bound dipeptidol monomer intermediate from d-2-hydroxyisovalerate and l-leucine. Further BbBSLS domains are predicted to catalyze the formation of the cyclic tetrameric ester bassianolide by recursive condensations of this monomer. Comparative infection assays against three selected insect hosts established bassianolide as a highly significant virulence factor of B. bassiana.
3. Aspergillus niger is a superior expression host for the production of bioactive fungal cyclodepsipeptides
Roderich D Süssmuth, Vera Meyer, David Schirmer, Lutz Adam, Lennart Richter, Simon Boecker, Daniel Petras, Tabea Schütze, Stefan Grätz, Dennis Kerwat Fungal Biol Biotechnol . 2018 Mar 2;5:4. doi: 10.1186/s40694-018-0048-3.
Background:Fungal cyclodepsipeptides (CDPs) are non-ribosomally synthesized peptides produced by a variety of filamentous fungi and are of interest to the pharmaceutical industry due to their anticancer, antimicrobial and anthelmintic bioactivities. However, both chemical synthesis and isolation of CDPs from their natural producers are limited due to high costs and comparatively low yields. These challenges might be overcome by heterologous expression of the respective CDP-synthesizing genes in a suitable fungal host. The well-established industrial fungusAspergillus nigerwas recently genetically reprogrammed to overproduce the cyclodepsipeptide enniatin B in g/L scale, suggesting that it can generally serve as a high production strain for natural products such as CDPs. In this study, we thus aimed to determine whether other CDPs such as beauvericin and bassianolide can be produced with high titres inA. niger, and whether the generated expression strains can be used to synthesize new-to-nature CDP derivatives.Results:The beauvericin and bassianolide synthetases were expressed under control of the tuneable Tet-on promoter, and titres of about 350-600 mg/L for bassianolide and beauvericin were achieved when using optimized feeding conditions, respectively. These are the highest concentrations ever reported for both compounds, whether isolated from natural or heterologous expression systems. We also show that the newly established Tet-on based expression strains can be used to produce new-to-nature beauvericin derivatives by precursor directed biosynthesis, including the compounds 12-hydroxyvalerate-beauvericin and bromo-beauvericin. By feeding deuterated variants of one of the necessary precursors (d-hydroxyisovalerate), we were able to purify deuterated analogues of beauvericin and bassianolide from the respectiveA. nigerexpression strains. These deuterated compounds could potentially be used as internal standards in stable isotope dilution analyses to evaluate and quantify fungal spoilage of food and feed products.Conclusion:In this study, we show that the product portfolio ofA. nigercan be expanded from enniatin to other CDPs such as beauvericin and bassianolide, as well as derivatives thereof. This illustrates the capability ofA. nigerto produce a range of different peptide natural products in titres high enough to become industrially relevant.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳