Menendez, N., Nur-e-Alam, M., Brana, A.F., Rohr, J.A. and Mendez, C. (2004) Tailoring Modification of Deoxysugars during Biosynthesis of the Antitumour Drug Chromomycin A3 by Streptomyces griseus ssp. Griseus. Molecular Microbiology, 53, 903-915.
http://dx.doi.org/10.1111/j.1365-2958.2004.04166.x

has been cited by the following article:

• TITLE: Spectroscopic and Calorimetric Approach to Understand the Molecular Basis of Self-Association of Aureolic Acid Antibiotic, Chromomycin A3

  AUTHORS: Shreyasi Dutta, Shibojyoti Lahiri, Dipak Dasgupta

  KEYWORDS: Oligomer; Neutral; Anionic; Circular Dichroism; Enthalpy; NMR Spectroscopy

  JOURNAL NAME: Open Journal of Biophysics, Vol.4 No.2, April 8, 2014

  ABSTRACT: Chromomycin A3 (CHR, pKa = 7.0), an aureolic acid group of antitumor antibiotic, undergoes self-association in aqueous solution in neutral and anionic forms. Self-association processes of neutral and anionic CHR have been studied in pH 5.0 and pH 9.0, respectively using different spectroscopic methods such as absorbance, fluorescence, CD, NMR and isothermal titration calorimetry (ITC). Results from these studies reveal that at low concentration (2 + CHR (CHR)3 and (CHR)3 + CHR (CHR)4. Analysis of NMR spectra of 100 μM and 1 mM CHR indicates that the self-association of CHR (neutral and anionic form) is most likely to happen via hydrophobic interaction involving the sugar moieties and surrounding water molecules. Calorimetric studies indicate that self-association of both anionic and neutral CHR is entropy driven. These observations imply that sugar substituents play a major role in their state of aggregation after biosynthesis from a gene cluster. The self-association features of the antibiotic have been compared with those of Mithramycin, an antibiotic of the same group.