New antibiotics produced by Bacillus subtilis strains

被引:5
作者
Malanicheva, I. A. [1 ]
Kozlov, D. G. [1 ]
Efimenko, T. A. [1 ]
Zenkova, V. A. [1 ]
Katrukha, G. S. [1 ]
Reznikova, M. I. [1 ]
Korolev, A. M. [1 ]
Borshchevskaya, L. N. [2 ]
Tarasova, O. D. [2 ]
Sineokii, S. P. [2 ]
Efremenkova, O. V. [1 ]
机构
[1] Russian Acad Med Sci, Gause Res Inst New Antibiot, Moscow, Russia
[2] Res Inst Genet & Select Ind Microorganisms, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
Bacillus subtilis; basidiomycetes; polypeptides; polyenes; antibiotic resistance in bacteria; MRSA; resistance to glycopeptide antibiotics;
D O I
10.1134/S0026261714040110
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Two Bacillus subtilis strains isolated from the fruiting body of a basidiomycete fungus Pholiota squarrosa exhibited a broad range of antibacterial activity, including those against methicillin-resistant Staphylococcus aureus INA 00761 (MRSA) and Leuconostoc mesenteroides VKPM B-4177 resistant to glycopeptide antibiotics, as well as antifungal activity. The strains were identified as belonging to the "B. subtilis" complex based on their morphological and physiological characteristics, as well as by sequencing the 16S rRNA gene fragments. Both strains (INA 01085 and INA 01086) produced insignificant amounts of polyene antibiotics (hexaene and pentaene, respectively). Strain INA 01086 also produced a cyclic polypeptide antibiotic containing Asp, Gly, Leu, Pro, Tyr, Thr, Trp, and Phe, while the antibiotic of strain INA 01085 contained, apart from these, two unidentified nonproteinaceous amino acids. Both polypeptide antibiotics were new compounds efficient against gram-positive bacteria and able to override the natural bacterial antibiotic resistance.
引用
收藏
页码:352 / 356
页数:5
相关论文
共 14 条
[1]   Diversity and applications of Bacillus bacteriocins [J].
Abriouel, Hikmate ;
Franz, Charles M. A. P. ;
Ben Omar, Nabil ;
Galvez, Antonio .
FEMS MICROBIOLOGY REVIEWS, 2011, 35 (01) :201-232
[2]   ANTIBIOTIC IDENTIFICATION - COMPUTERIZED DATA-BASE SYSTEM [J].
BOSTIAN, M ;
MCNITT, K ;
ASZALOS, A ;
BERDY, J .
JOURNAL OF ANTIBIOTICS, 1977, 30 (07) :633-634
[3]   Drug discovery from natural sources [J].
Chin, Young-Won ;
Balunas, Marcy J. ;
Chai, Hee Byung ;
Kinghorn, A. Douglas .
AAPS JOURNAL, 2006, 8 (02) :E239-E253
[4]  
Egorov N. S., 1999, Antibiotiki i Khimioterapiya, V44, P33
[5]   DIGESTION OF RHIZOCTICINS TO (Z)-L-2-AMINO-5-PHOSPHONO-3-PENTENOIC ACID - REVISION OF THE ABSOLUTE-CONFIGURATION OF PLUMBEMYCIN-A AND PLUMBEMYCIN-B [J].
FREDENHAGEN, A ;
ANGST, C ;
PETER, HH .
JOURNAL OF ANTIBIOTICS, 1995, 48 (09) :1043-1045
[6]   STRUCTURAL CHARACTERIZATION OF BACITRACIN COMPONENTS BY FRIT-FAST ATOM BOMBARDMENT (FAB) LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY (LC/MS) [J].
IKAI, Y ;
OKA, H ;
HAYAKAWA, J ;
HARADA, K ;
SUZUKI, M .
JOURNAL OF ANTIBIOTICS, 1992, 45 (08) :1325-1334
[7]   BACITRACIN - A NEW ANTIBIOTIC PRODUCED BY A MEMBER OF THE B-SUBTILIS GROUP [J].
JOHNSON, BA ;
ANKER, H ;
MELENEY, FL .
SCIENCE, 1945, 102 (2650) :376-377
[8]  
Patrick F., 2012, AM J BIOCH BIOTECHNO, V8, P40, DOI [DOI 10.3844/AJBBSP.2012.40.46, 10.3844/ajbbsp.2012.40.46, 10.3844/ajbbsp.2012.38.43, DOI 10.3844/AJBBSP.2012.38.43]
[9]   Natural functions of lipopeptides from Bacillus and Pseudomonas: more than surfactants and antibiotics [J].
Raaijmakers, Jos M. ;
de Bruijn, Irene ;
Nybroe, Ole ;
Ongena, Marc .
FEMS MICROBIOLOGY REVIEWS, 2010, 34 (06) :1037-1062
[10]  
Rea MC, 2011, PROKARYOTIC ANTIMICROBIAL PEPTIDES: FROM GENES TO APPLICATIONS, P29, DOI 10.1007/978-1-4419-7692-5_3