Neocarzinostatin

Neocarzinostatin chromophore[1]
Structural formula of neocarzinostatin
Space-filling model of the neocarzinostatin molecule
Names
IUPAC name
(1aS,5R,6R,6aE)-6-{[(2R,3R,4R,5R,6R)-4,5-Dihydroxy-6-methyl-3-(methylamino)tetrahydro-2H-pyran-2-yl]oxy}-1a-(2-oxo-1,3-dioxolan-4-yl)-2,3,8,9-tetradehydro-1a,5,6,9a-tetrahydrocyclopenta[5,6]cyclonona[1,2-b]oxiren-5-yl 2-hydroxy-7-methoxy-5-methyl-1-naphthoate
Identifiers
79633-18-4 Neocarzinostatin chromophore N
9014-02-2 Neocarzinostatin N
3D model (Jmol) Interactive image
ChemSpider 394601 N
PubChem 447545
Properties
C35H33NO12
Molar mass 659.64 g/mol
Pharmacology
Pharmacokinetics:
Renal
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Neocarzinostatin (NCS) is a macromolecular chromoprotein enediyne antitumor antibiotic secreted by Streptomyces macromomyceticus.

It consists of two parts, a labile chromophore (the non-protein molecular entity shown at right) and a 113 amino acid protein to which the chromophore is tightly and non-covalently bound with high affinity (Kd ~ 10−10 M). The non-protein component is a very potent DNA-damaging agent; However it is extremely unstable and the role of the protein is to protect it and release it to the target DNA. Opening of the epoxide under reductive conditions present in cells creates favorable conditions for a Bergman cyclization, that leads to formation of benzyne, Followed by DNA strand cleavage. Another important member of the chromoprotein group of natural products is kedarcidin.

As a medicine it is among the most potent, and in Japan only it has been used against liver cancer clinically.

Biosynthesis of NCS Chromophore

A schematic outline of stepwise synthesis of NCS Chromophore

The biosynthesis of Neocarzinostatin Chromophore takes place through a convergence of the activities of a gene cluster, which includes, two separate iterative type I polyketide synthase (PKS) and deoxy sugar biosynthetic pathways. The first type I PKS gene NcsE codes for the enediyne moiety. The second type I PKS gene NcsB codes for the naphthoic acid moiety. Additionally, a cluster of NcsC genes are responsible for coding enzymes for the synthesis of the deoxyamino sugar moiety of NCS chromophore.[2] The biosynthesis of NCS Chromophore can be divided into three stages:

1.Synthesis of deoxyaminosugar moiety: This part is carried out by the enzymes encoded by a cluster of seven genes, named NcsC through Ncs6. Since, these enzymes have similarity to dNDP-D-mannose synthases, it has been proposed that, the synthesis starts from D-mannose-1-phosphate. Since the C-2 hydroxyl group (-OH) is ultimately eliminated, the possibility of having D-glucose-1-phosphate cannot also be ruled out. However, additional studies indicate that, D-mannose-1-phosphate is the more likely starting point.

2.Synthesis of naphthoic acid moiety: A group of four genes, namely, NcsB, NcsB1, NcsB2 and NcsB3 encode enzymes for the synthesis of the naphthoic acid moiety. Although, from the aromatic structure of naphthoic acid moiety, it might appear that it is synthesized by a type II PKS, the NcsB enzymes in fact constitute an iterative type I PKS. This is similar to other enediyne natural products.[3] The methyl group on the phenol group is added by SAM.

3.Synthesis of enediyne moiety and convergent assembly: The enediyne is synthesized by 14 enzymes encoded by NcsE to NcsE11 plus NcsF1 and NcsF2. NcsE to NcsE11 constitute another iterative type I PKS, while NcsF1 and NcsF2 have epoxides hydrolase activity. Finally, the building blocks are assembled in a convergent fashion. Ncs6 glycosyltransferase catalyzes the coupling between the enediyne core and the dNDP-deoxyaminosugar. The naphthoyl group is attached to the enediyne core by the enzyme NcsB2 CoA Ligase. There is an additional carbonate functionality added, probably originating from CO2 (or bicarbonate), however, it is not clear whether that step is enzymatic.

References

  1. ↑ Shoji Kobayashi; Makiko Hori; Guang Xing Wang & Masahiro Hirama (2006). "Formal Total Synthesis of Neocarzinostatin Chromophore". J. Org. Chem. 71 (2): 636–644. doi:10.1021/JO052031O. PMID 16408974.
  2. ↑ Liu, W; Nonaka, K; Christenson, SD; Shen, B (25 Mar 2005). "The neocarzinostatin biosynthetic gene cluster from Streptomyces carzinostaticus ATCC 15944 involving two iterative type I polyketide synthases". Chem Biol. 12: 293–302. doi:10.1016/j.chembiol.2004.12.013. PMID 15797213.
  3. ↑ Horsman, GP; Chen, Y; Thorson, JS; Shen, B (Jun 22, 2010). "Polyketide synthase chemistry does not direct biosynthetic divergence between 9- and 10-membered enediynes". Proc Natl Acad Sci U S A. 107 (25): 11331–5. doi:10.1073/pnas.1003442107. PMC 2895059Freely accessible. PMID 20534556.
This article is issued from Wikipedia - version of the 7/31/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.