Purification and biochemical characterization of mutacin I from the group I strain of Streptococcus mutans, CH43, and genetic analysis of mutacin I biosynthesis genes

被引:77
作者
Qi, FX [1 ]
Chen, P [1 ]
Caufield, PW [1 ]
机构
[1] Univ Alabama Birmingham, Sch Dent, Dept Oral Biol, Birmingham, AL 35294 USA
关键词
D O I
10.1128/AEM.66.8.3221-3229.2000
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Previously, we reported isolation and characterization of mutacin III: and genetic analysis of mutacin III biosynthesis genes from the group III strain of Streptococcus mutans, UA787 (F. Qi, P. Chen, and P. W. Caufield, Appl. Environ. Microbiol. 65:3880-3887, 1999). During the same process laf isolating the mutacin III structural gene, we also cloned the structural gene for mutacin I. In this report, we present purification and biochemical characterization of mutacin I from the group I strain CH43 and compare mutacin I and mutacin III biosynthesis genes. The mutacin I biosynthesis gene locus consists of 14 genes in the order mutR, -A, -A', -B, C, -D, -P, -T, -F, -E, -G, orfX, orfY, orfZ. mutA is the structural gene for mutacin I, while mutA' is not required for mutacin I activity. DNA and protein sequence analysis revealed that mutacins I and In are homologous to each other, possibly arising from a common ancestor. The mature mutacin I is 24 amino acids in size and has a molecular mass of 2,364 Da. Ethanethiol modification and peptide sequencing of mutacin I revealed that it contains six dehydrated serines, four of which are probably involved with thioether bridge formation. Comparison of the primary sequence of mutacin I with that of mutacin III and epidermin suggests that mutacin I likely has the same bridging pattern as epidermin.
引用
收藏
页码:3221 / 3229
页数:9
相关论文
共 38 条
[1]   EPIDERMIN - SEQUENCING OF A HETERODET TETRACYCLIC 21-PEPTIDE AMIDE ANTIBIOTIC [J].
ALLGAIER, H ;
JUNG, G ;
WERNER, RG ;
SCHNEIDER, U ;
ZAHNER, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 160 (01) :9-22
[2]   ROLE OF THE LEADER AND STRUCTURAL REGIONS OF PRELANTIBIOTIC PEPTIDES AS ASSESSED BY EXPRESSING NISIN-SUBTILIN CHIMERAS IN BACILLUS-SUBTILIS-168, AND CHARACTERIZATION OF THEIR PHYSICAL, CHEMICAL, AND ANTIMICROBIAL PROPERTIES [J].
CHAKICHERLA, A ;
HANSEN, JN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23533-23539
[3]  
Chen P, 1999, APPL ENVIRON MICROB, V65, P1356
[4]  
CREIGHTON TE, 1983, PROTEINS STRUCTURE M, P235
[5]   Functional analysis of promoters in the nisin gene cluster of Lactococcus lactis [J].
deRuyter, PGGA ;
Kuipers, OP ;
Beerthuyzen, MM ;
vanAlenBoerrigter, I ;
deVos, WM .
JOURNAL OF BACTERIOLOGY, 1996, 178 (12) :3434-3439
[6]   MATURATION PATHWAY OF NISIN AND OTHER LANTIBIOTICS - POSTTRANSLATIONALLY MODIFIED ANTIMICROBIAL PEPTIDES EXPORTED BY GRAM-POSITIVE BACTERIA [J].
DEVOS, WM ;
KUIPERS, OP ;
VANDERMEER, JR ;
SIEZEN, RJ .
MOLECULAR MICROBIOLOGY, 1995, 17 (03) :427-437
[7]   STRUCTURE OF NISIN [J].
GROSS, E ;
MORELL, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1971, 93 (18) :4634-+
[8]  
GROSS E, 1968, Febs Letters, V2, P61, DOI 10.1016/0014-5793(68)80101-2
[9]   ORGANIZATION OF THE FIMBRIAL GENE REGION OF BACTEROIDES-NODOSUS - CLASS-I AND CLASS-II STRAINS [J].
HOBBS, M ;
DALRYMPLE, BP ;
COX, PT ;
LIVINGSTONE, SP ;
DELANEY, SF ;
MATTICK, JS .
MOLECULAR MICROBIOLOGY, 1991, 5 (03) :543-560
[10]   CLONING OF THE GENE ENCODING STREPTOCOCCIN A-FF22, A NOVEL LANTIBIOTIC PRODUCED BY STREPTOCOCCUS-PYOGENES, AND DETERMINATION OF ITS NUCLEOTIDE-SEQUENCE [J].
HYNES, WL ;
FERRETTI, JJ ;
TAGG, JR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (06) :1969-1971