Covalent structure of mutacin 1140 and a novel method for the rapid identification of lantibiotics

被引:41
作者
Smith, L
Novák, J
Rocca, J
McClung, S
Hillman, JD
Edison, AS
机构
[1] Univ Florida, Coll Med, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Neurosci, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Med, Inst Brain, Gainesville, FL 32610 USA
[4] Univ Florida, Coll Med, Interdisciplinary Ctr Biol Res Prot Chem Core, Gainesville, FL 32610 USA
[5] Univ Florida, Coll Dent, Dept Oral Biol, Gainesville, FL 32610 USA
[6] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2000年 / 267卷 / 23期
关键词
bacteriocin; double-labeling; mass spectrometry; NMR; structure determination;
D O I
10.1046/j.1432-1033.2000.01777.x
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 primary structure of the Streptococcus mutans lantibiotic mutacin 1140 was elucidated by NMR spectroscopy, mass spectrometry, and chemical sequencing. The structure is in agreement with other closely related lantibiotics, such as epidermin. A novel method was developed in which mutacin 1140 was chemically modified with sodium borohydride followed by ethanethiol, allowing the differentiation of the thioether-containing residues from the dehydrated residues. This double-labeling strategy provides a simple method to reliably identify all modified lantibiotic residues with a minimal amount of material. While NMR spectroscopy is still required to obtain thioether bridging patterns and thus the complete covalent structure, the double-labeling technique, along with mass spectrometry, provides most of the information in a fraction of the time required for a complete NMR analysis. Thus, with these new techniques lantibiotics can be rapidly characterized.
引用
收藏
页码:6810 / 6816
页数:7
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