Distribution of microbes producing antimicrobial ε-poly-L-lysine polymers in soil microflora determined by a novel method

被引:107
作者
Nishikawa, M [1 ]
Ogawa, K [1 ]
机构
[1] RIBS, Okayama 7161241, Japan
关键词
D O I
10.1128/AEM.68.7.3575-3581.2002
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 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
We developed a simple and sensitive screening method to investigate the distribution of microbes producing an antimicrobial poly(amino acid), epsilon-poly-L-lysine (epsilon-PL), in microflora. An acidic dye, Poly R-478, incorporated in an agar plate detected epsilon-PL producers by electrostatic interaction with the secreted basic polymers. All epsilon-PL producers, isolated after careful and sufficient screening of soil microflora, belonged exclusively to two groups of bacteria of the family Streptomycetaceae and ergot fungi. They were characterized based on the density and diameter of the concentric zone formed by the secreted polymers. The density depended on each isolate. The increase in the diameter of the concentric zone per unit of time varied among isolates and was negatively correlated with the molecular weight. Although the distribution of epsilon-PL producers was extremely limited, their products were structurally varied. The molecular masses of the secreted polymers among the isolates ranged from 0.8 to 2.0 kDa. There were also isolates producing unknown polymers inconsistent with the correlation or producing a mixture of polymers with original and modified structures. A chemically modified polymer was an epsilon-PL derivative, as determined by mass spectrometry. Since the structural variations had no relation to the phylogenetic position of the isolates, it is possible that enzymes involved in the synthesis diversified after putative horizontal transfers of relevant genes.
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页码:3575 / 3581
页数:7
相关论文
共 14 条
[1]
A poly-γ-glutamate synthetic system of Bacillus subtilis IFO 3336:: Gene cloning and biochemical analysis of poly-γ-glutamate produced by Escherichia coli clone cells [J].
Ashiuchi, M ;
Soda, K ;
Misono, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 263 (01) :6-12
[2]
The C-terminal region of nisin is responsible for the initial interaction of nisin with the target membrane [J].
Breukink, E ;
vanKraaij, C ;
Demel, RA ;
Siezen, RJ ;
Kuipers, OP ;
deKruijff, B .
BIOCHEMISTRY, 1997, 36 (23) :6968-6976
[3]
DEFENSINS PROMOTE FUSION AND LYSIS OF NEGATIVELY CHARGED MEMBRANES [J].
FUJII, G ;
SELSTED, ME ;
EISENBERG, D .
PROTEIN SCIENCE, 1993, 2 (08) :1301-1312
[4]
Hiraki J, 1998, SEIBUTSU-KOGAKU KAIS, V76, P487
[5]
INFLUENCE OF CULTURE PARAMETERS ON LIGNIN METABOLISM BY PHANEROCHAETE-CHRYSOSPORIUM [J].
KIRK, TK ;
SCHULTZ, E ;
CONNORS, WJ ;
LORENZ, LF ;
ZEIKUS, JG .
ARCHIVES OF MICROBIOLOGY, 1978, 117 (03) :277-285
[6]
Occurrence of ε-polu-L-lysine-degrading enzyme in ε-poly-L-lysine-tolerant Sphingobacterium multivorum OJ10:: purification and characterization [J].
Kito, M ;
Onji, Y ;
Yoshida, T ;
Nagasawa, T .
FEMS MICROBIOLOGY LETTERS, 2002, 207 (02) :147-151
[7]
KITO M, 2001, P ANN M SOC BIOSC BI, P142
[8]
MOLECULAR CHARACTERIZATION AND PROTEIN-ANALYSIS OF THE CAP REGION, WHICH IS ESSENTIAL FOR ENCAPSULATION IN BACILLUS-ANTHRACIS [J].
MAKINO, S ;
UCHIDA, I ;
TERAKADO, N ;
SASAKAWA, C ;
YOSHIKAWA, M .
JOURNAL OF BACTERIOLOGY, 1989, 171 (02) :722-730
[9]
PHYSICOCHEMICAL DETERMINANTS FOR THE INTERACTIONS OF MAGAININS-1 AND MAGAININS-2 WITH ACIDIC LIPID BILAYERS [J].
MATSUZAKI, K ;
HARADA, M ;
FUNAKOSHI, S ;
FUJII, N ;
MIYAJIMA, K .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1063 (01) :162-170
[10]
POLY-L-LYSINE PRODUCED BY STREPTOMYCES .2. TAXONOMY AND FERMENTATION STUDIES [J].
SHIMA, S ;
SAKAI, H .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1981, 45 (11) :2497-2502