Copper(II)-based metal affinity chromatography for the isolation of the anticancer agent bleomycin from Streptomyces verticillus culture

被引:20
作者
Gu, Jiesi
Codd, Rachel [1 ]
机构
[1] Univ Sydney, Sch Med Sci Pharmacol, Sydney, NSW 2006, Australia
关键词
Metal affinity chromatography; Bleomycin; Copper complexes; Green chemistry; ACTIVATED BLEOMYCIN; ANTIBIOTIC NC0604; CRYSTAL-STRUCTURE; COMPLEX; DNA; BINDING; SPECTROSCOPY; TALLYSOMYCIN; PEROXIDE; LIGANDS;
D O I
10.1016/j.jinorgbio.2012.01.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The glycopeptide-based bleomycins are structurally complex natural products produced by Streptomyces verticillus used in combination therapy against testicular and other cancers. Bleomycin has a high affinity towards a range of transition metal ions with the 1:1 Fe(II) complex relevant to its mechanism of action in vivo and the 1:1 Cu(II) complex relevant to its production from culture. The affinity between Cu(II) and bleomycin was the underlying principle for using Cu(II)-based metal affinity chromatography in this work to selectively capture bleomycin from crude S. verticillus culture. A solution of standard bleomycin was retained at a binding capacity of 300 nmol mL(-1) on a 1-mL bed volume of Cu(II)-loaded iminodiacetate (IDA) resin at pH 9 via the formation of the heteroleptic immobilized complex [Cu(IDA)(bleomycin)]. Bleomycin was eluted from the resin at pH 5 as the metal-free ligand under conditions where pK(a) (IDA) < pH< pK(a)beta-hydroxyhistidine amide (bleomycin). Bleomycin was captured on a Cu(II)-loaded IDA resin at pH 9 in 50% yield from bleomycin-containing S. verticillus culture that was pre-processed using XAD-2 resin to remove endogenously bound Cu(II). The approximate 25-fold purification of bleomycin from complex culture supernatant under aqueous conditions in a single step demonstrates the potential of Cu(II)-based metal affinity chromatography as a green chemistry platform for streamlined access to this high-value therapeutic agent. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:198 / 203
页数:6
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