Diversity of Endophytic Actinomycetes Isolated from Roots and Root Nodules of Pueraria candollei Grah. ex Benth. and the Analyses of Their Secondary Metabolites

被引:0
作者
Boonsnongcheep, Panitch [1 ]
Nakashima, Takuji [2 ]
Takahashi, Yoko [2 ]
Prathanturarug, Sompop [1 ]
机构
[1] Mahidol Univ, Fac Pharm, Dept Pharmaceut Bot, 447 Sri Ayuthaya Rd, Bangkok 10400, Thailand
[2] Kitasato Univ, Kitasato Inst Life Sci, Minato Ku, 5-9-1 Shirokane, Tokyo 1088641, Japan
来源
CHIANG MAI JOURNAL OF SCIENCE | 2017年 / 44卷 / 01期
关键词
endophytes; actinomycetes; physicochemical screening; secondary metabolites; S-ADENOSYLMETHIONINE; CULTURE BROTH; MICROMONOSPORA; BACTERIA; METHYLTRANSFERASES; FERMENTATION; ENUMERATION; INHIBITORS; ANALOGS;
D O I
暂无
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pueraria candollei Grah. ex Benth. is a Thai herb that contributes to many phytoestrogenic-related pharmacological activities. In this study, the diversity of endophytic actinomycetes from roots and root nodules of P. candollei and actinomycetes from rhizospheric soils were investigated. Moreover, the secondary metabolites production of these isolated actinomycetes was investigated. A total of 85 isolates were obtained from roots, root nodules and rhizospheric soils, 32 from the roots of P. candollei var. candollei, 26 from the root nodules of P. candollei var. mirifica and 27 from rhizospheric soil samples. Partial 16S rRNA sequence data revealed that the isolated actinomycetes were distributed among 7 genera including, Streptomyces, Micromonospora, Verrucosispora, Microbispora, Nonomuraea, Plantactinospora and Shimazuella. The majority of isolates from plant sources were members of the genus Micromonospora. Broth extracts of these isolates were analyzed using LC/UV and LC/MS. The physicochemical properties of 10 selected peaks were searched in the database. The physicochemical properties of some peaks were matched with known microbial metabolites. The structure of an unknown compound was elucidated using spectroscopic data. The NMR data indicated the presence of N-acetylhomocysteine moiety and the compound was determined to be S-adenosyl-N-acetylhomocysteine. This compound was isolated from Micromonospora for the first time. In conclusion, this work contributed to the known information on the diversity of actinomycetes associated with P. candollei and their capability for secondary metabolite production.
引用
收藏
页数:14
相关论文
共 29 条
[1]   METHIONINE METABOLISM IN APPLE TISSUE - IMPLICATION OF S-ADENOSYLMETHIONINE AS AN INTERMEDIATE IN CONVERSION OF METHIONINE TO ETHYLENE [J].
ADAMS, DO ;
YANG, SF .
PLANT PHYSIOLOGY, 1977, 60 (06) :892-896
[2]  
Bérdy J, 2012, J ANTIBIOT, V65, P385, DOI [10.1038/ja.2012.27, 10.1038/ja.2012.54]
[3]   POTENTIAL INHIBITORS OF S-ADENOSYLMETHIONINE-DEPENDENT METHYLTRANSFERASES .1. MODIFICATION OF AMINO-ACID PORTION OF S-ADENOSYLHOMOCYSTEINE [J].
BORCHARDT, RT ;
WU, YS .
JOURNAL OF MEDICINAL CHEMISTRY, 1974, 17 (08) :862-868
[4]   WINOGRADSKY SALTS SOLUTION AS A DILUTING MEDIUM FOR PLATE-COUNT OF OLIGOTROPHIC BACTERIA IN SOIL [J].
DABEKSZRENIAWSKA, M ;
HATTORI, T .
JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY, 1981, 27 (06) :517-518
[5]   Endophytic actinobacteria of medicinal plants: diversity and bioactivity [J].
Golinska, Patrycja ;
Wypij, Magdalena ;
Agarkar, Gauravi ;
Rathod, Dnyaneshwar ;
Dahm, Hanna ;
Rai, Mahendra .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2015, 108 (02) :267-289
[6]  
Govindasamy V., 2014, ADV ENDOPHYTIC RES, P27, DOI DOI 10.1007/978-81-322-1575-2_2
[7]  
Hall T. A., NUCL ACIDS S SER, V41, P95, DOI DOI 10.1021/BK-1999-0734.CH008
[8]   The Hidden World within Plants: Ecological and Evolutionary Considerations for Defining Functioning of Microbial Endophytes [J].
Hardoim, Pablo R. ;
van Overbeek, Leonard S. ;
Berg, Gabriele ;
Pirttila, Anna Maria ;
Compant, Stephane ;
Campisano, Andrea ;
Doering, Matthias ;
Sessitsch, Angela .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2015, 79 (03) :293-320
[9]  
Hasegawa S., 2006, Actinomycetologia, V20, P72, DOI DOI 10.3209/SAJ.20.72
[10]   SYNTHESIS OF INHIBITORS OF METHYLTRANSFERASES - ANALOGS OF S-ADENOSYL HOMOCYSTEINE [J].
HILDESHEIM, J ;
HILDESHEIM, R ;
LEDERER, E .
BIOCHIMIE, 1971, 53 (10) :1067-+