

FOLLOWUS
1. State Key Laboratory of Marine Environmental Science Xiamen University
2. College of Ocean and Earth Sciences Xiamen University
网络首发:2013-05-08,
纸质出版:2013
Scan QR Code
Antimicrobial activities of novel cultivable bacteria isolated from marine sponge Tedania anhelans[J]. 海洋湖沼学报(英文), 2013,31(3):581-590.
Zeng, Z., Zhao, J., Ke, C. et al. Antimicrobial activities of novel cultivable bacteria isolated from marine sponge Tedania anhelans, ., Chin. J. Ocean. Limnol. 31, 581–590 (2013). https://doi.org/10.1007/s00343-013-2223-y
Antimicrobial activities of novel cultivable bacteria isolated from marine sponge Tedania anhelans[J]. 海洋湖沼学报(英文), 2013,31(3):581-590. DOI: 10.1007/s00343-013-2223-y.
Zeng, Z., Zhao, J., Ke, C. et al. Antimicrobial activities of novel cultivable bacteria isolated from marine sponge Tedania anhelans, ., Chin. J. Ocean. Limnol. 31, 581–590 (2013). https://doi.org/10.1007/s00343-013-2223-y DOI:
Marine sponge Tedania anhelans distributes throughout the intertidal zone of Fujian
southeastern China
and is a potential source of natural bioactive products. The sponge harbors a large number of bacterial groups that have been identified using various techniques
including fluorescent in situ hybridization (FISH). Fractionation of dissociated sponge allowed isolation of 25 bacterial species. Based on 16S rRNA gene sequencing
phylogenetic analysis attributed most of these eubacteria to α-Proteobacteria
γ-Proteobacteria
Cytophaga / Flavobacterium / Bacteroidetes (CFB group)
and the family Bacillaceae of Gram-positive bacteria. In sequence similarity
five putatively novel species were identified with less than 98% similarity to other strains in the NCBI database. Tests for antimicrobial activities were performed against Gram-positive bacteria
Gram-negative bacteria
fungi
antitumor indicators Escherichia coli 343/591 (with DNA repair deficiency)
regular E. coli 343/636 (with different DNA repair capacity)
and 10 bacterial isolates exhibited inhibitory bioactivities. Among these strains
three isolates were detected involving function gene NRPS-A domains
which were most closely related to the amino acid sequences of linear gramicidin synthetase and pyoverdine synthetase. These results contribute to our knowledge of the microbes associated with marine sponges and further reveal novel bacterial resources for the screening of bioactive marine natural products.
Amann R I, Krumholz L, Stahl D A. 1990. Fluorescentoligonucleotide probing of whole cells for determinative, phylogenetic, and environmental studies in microbiology. J. Bacterial., 172: 762–770.
Blunt J W, Copp B R, Munro M H G, Northcote P T, Prinsep M R. 2003. Marine natural products. Nat. Prod. Rep., 20: 1–48.
Brinkhoff T, Giebel H A, Simon M. 2008. Diversity, ecology, and genomics of the Roseobacter clade: a short overview. Arch. Microbiol., 189: 531–539.
Budzikiewicz H. 1993. Secondary metabolites from fluorescent pseudomonads. FEMS Microbiol. Lett., 104: 209–228.
Chun J, Lee J H, Jung Y, Kim M, Kim S, Kim B K, Lim Y W. 2007. EzTaxon: a web-based tool for the identification of prokaryotes based on 16S ribosomal RNA gene sequences. Int. J. Syst. Evol. Microbiol., 57: 2 259–2 261.
DeLong E F. 1992. Archaea in coastal marine environments. Proc. Natl. Acad. Sci. USA, 89: 5 685–5 689.
Devi P, Wahidullah S, Rodrigues C, Souza L D. 2010. The sponge-associated bacterium Bacillus licheniformis SAB1: a source of antimicrobial compounds. Mar. Drugs, 8: 1 203–1 212.
El Sayed K A, Kelly M, Kara U A K, Ang K K H, Katsuyama T, Dumbar D C, Khan A A, Hamann M T. 2001. New manzamine alkaloids with potent activity against infectious diseases. J. Am. Chem. Soc., 123: 1 804–1 808.
Eric W S, Carole A B, D J F. 1998. Theopalauamide, a bicyclic glycopeptide from filamentous bacterial symbionts of the lithistid sponge Theonella swinhoei from Palau and Mozambique. J. Org. Chem. 63: 1 254–1 258.
Erin A G, William F, Paul R J. 2007. Phylogenetic diversity of gram-positive bacteria cultured from marine sediments. Appl. Environ. Microbiol., 73: 3 272–3 282.
Faulkner D J, He H Y, Unson M D, Bewley C A, Garson M J. 1993. New metabolites from marine sponges: are symbionts important? Gazzetta. Chimica. Italiana, 123: 301–307.
Flemer B, Kennedy J, Margassery L M, Morrissey J P, O’Gara F, Dobson A D W. 2012. Diversity and antimicrobial activities of microbes from two Irish marine sponges, Suberites carnosus and Leucosolenia sp. J. Appl. Microbiol., 112: 289–301.
Flowers A E, Garson M J, Webb R I, Dumdei E J, Charan R D. 1998. Cellular origin of chlorinated diketopiperazines in the dictyoceratid sponge Dysidea herbacea (Keller). Cell Tissue. Res., 292: 597–607.
Gontang E A, Fenical W, Jensen P R. 2007. Phylogenetic diversity of gram-positive bacteria cultured from marine sediments. Appl. Environ. Microbiol., 73: 3 272–3 282.
Gram L, Melchiorsen J, Bruhn J B. 2010. Antibacterial activity of marine culturable bacteria collected from a global sampling of ocean surface waters and surface swabs of marine organisms. Mar. Biotechnol., 12: 439–451.
Hathout Y, Ho Y P, Kyzho V, Demirev P, Fenselau C. 2000. Knrstakins: a new class of lipopeptides isolated from Bacillus thruringiensis. J. Nat. Prod., 63: 1 492–1 496.
Jesper B B, Lone G, Robert B. 2007. Production of antibacterial compounds and biofilm formation by Roseobacter species are influenced by culture conditions. Appl. Environ. Microbiol., 73: 442–450.
Kennedy J, Baker P, Piper C, Cotter P D, Walsh M, Mooij M J, Bourke M B, Rea M C, O’Connor, P M, Ross R P, Hill C, O’Gara F, Marchesi J R, Dobson A D. 2009. Isolation and analysis of bacteria with antimicrobial activities from the marine sponge Haliclona simulans collected from Irish waters. Mar. Biotechnol., 11: 384–396.
Lebbadi M, Galvez A, Maqueda M, Martinez-Bueno M, Valdivia E. 1994. Fungicin M4: a narrow spectrum peptide antibiotic from Bacillus lichenformis M-4. J. Appl. Bacteriol., 17: 49–53.
Lee O O, Wang Y, Yang J, LafiF F, Al-Sawailem A, Qian P Y. 2011. Pyrosequencing reveals highly diverse and speciesspecific microbial communities in sponges from the Red Sea. ISME J., 5: 650–664.
Li Z Y, He L M, Miao X L. 2007. Cultivable bacterial community from South China Sea sponge as revealed by DGGE fingerprinting and 16S rDNA phylogenetic analysis. Curr. Microbiol., 55: 465–472.
Manuel M G, Marta D V, Gerhard W, Alfonso R E, Josefa A. 2007. Microbial community associated with the colonial ascidian Cystodytes dellechiajei. Environ. Microbiol., 9: 521–534
Marinho P R, Moreira A P B, Pellegrino FLPC, Muricy G, Bastos M C F, dos Santos K R N, Giambiagi-deMarval M, Laport M S. 2009. Marine Pseudomonas putida: a potential source of antimicrobial substances against antibiotic-resistant bacteria. Mem. Inst. Oswaldo. Cruz., Rio. De. Janeiro., 104: 678–682.
Meyer B, Kuever J. 2008. Phylogenetic diversity and spatial distribution of the microbial community associated with the Caribbean deep-water sponge Polymastia cf. corticata by 16S rRNA, aprA, and amoA gene analysis. Microb. Ecol., 56: 306–321.
Michael W T, Regina R, Doris S, Michael W. 2007. Spongeassociated microorganisms: evolution, ecology and biotechnological potential. Microbiol. Mol. Biol. R., 71: 295–347.
Moffitt M C, Neilan B A. 2001. On the presence of peptide synthetase and polyketide synthase genes in the cyanobacterial genus Nodularia. FEMS Microbiol. Lett., 196: 207–214.
Mosmann F. 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assay. J. Immunol. Methods, 65: 55–65.
Muramatsu Y, Uchino Y, Kasai H, Suzuki K, Nakagawa Y. 2007. Ruegeria mobilis sp. nov., a member of the Alphaproteobacteria isolated in Japan and Palau. Int. J. Syst. Evol. Microbiol., 57: 1 304–1 309.
Neilan B A, Dittmann E, Rouhiainen L, Bass R A, Schaub V, Sivonen K, Borner T. 1999. Nonribosomal peptide synthesis and toxigenicity of cyanobacteria. J. Bacterial., 181: 4 089–4 097.
Newman D J, Hill R T. 2006. New drugs from marine microbes: the tide is turning. J. Ind. Microbiol. Biotechnol., 33: 539–544.
Pabel C T, Vater J, Wilde C, Franke P, Hofemeister J, Adler B, Bringmann G, Hacker J, Hentschel U. 2003. Antimicrobial activities and matrix-assisted laser desorption/ionization mass spectrometry of Bacillus isolates from the marine sponge Aplysina aerophoba. Mar. Biotechnol., 5: 424–434.
Parameswaran P S, Naik C G, Vinod R H. 1997. Secondary metabolites from the sponge Tedania anhelans: isolation and characterization of two novel pyrazole acids and other metabolites. J. Nat. Prod., 60: 802–803.
Phelan R W, Clarke C, Morrissey J P, Dobson A D, O’Gara F, Barbosa T M. 2011. Tetracycline resistance-encoding plasmid from Bacillus sp. #24, isolated from the marine sponge Haliclona simulans. Appl. Environ. Microbiol., 77: 327–329.
Piel J. 2004. Metabolites from symbiotic bacteria. Nat. Prod. Rep., 21: 519–538.
Piel J, Hui D, Wen G, Butzke D, Matthias P, Fusetani N, Matsunaga S. 2004. Antitumor polyketide biosynthesis by an uncultivated bacterial symbiont of the marine sponge Theonella swinhoei. PNAS, 46: 16 222–16 227.
Pitcher D G, Saunders N A, Owen R J. 1989. Rapid extraction of bacterial genomic DNA with guanidium thiocyanate. Lett. Appl. Microbiol., 8: 151–156.
Roller C M, Wagner R, Amann W, Ludwig W, Schleifer K H. 1994. In situ probing of gram-positive bacteria with high DNA G+C content using 23S rRNA-targeted oligonucleotides. Microbiol., 140: 2 849–2 858.
Schmitz F J, Gunasekhera S P, Yalamanchii G, Hossain M B, Vanderhelm D. 1984. Tedanolide: a potent cytotoxic macrolide from the Caribbean sponge Tedania ignis. J. Am. Chem. Soc., 106: 7 251–7 252.
Silby M W, Cerdeno-Tarraga A M, Vernikos G S, Giddens S R, Jackson R W, Preston G. M, Zhang X X, Moon C D, Godfrey S A C, Knight C G, Malone J G, Robinson Z, Spiers A J, Harris S, Challis G. L, Yaxley A M, Harris D, Seeger K, Murphy L, Rutter S, Squares R, Saunders E, Mavromatis K, Brettin T S, Bentley S D, Thomson N R. 2009. Genomic and genetic analyses of diversity and plant interactions of Pseudomonas fluorescens. Genome Biology, 10: 1–16.
Taylor M W, Radax R, Steger D, Wagner M. 2007. Sponge associated microorganisms: evolution, ecology and biotechnological potential. Microbiol. Mol. Biol. Rev., 71: 295–347.
Thomas T R A, Kavlekar D P, LokaBharathi P A. 2010. Marine drugs from sponge-microbe association-a review. Mar. Drugs, 8: 1 417–1 468.
Webster N S, Hill R T. 2001. The culturable microbial community of the Great Barrier Reef sponge Rhopaloeides odorabile is dominated by an α-proteobacterium. Mar. Biol., 138: 843–851.
Webster N S, Watts J E M, Hill R T. 2001a. Detection and phylogenetic analysis of novel Crenarchaeote and Euryarchaeote 16S ribosomal RNA gene sequences from a Great Barrier Reef sponge. Mar. Biotechnol, 3: 600–608.
Webster N S, Wilson K J, Blackall L L, Hill R T. 2001b. Phylogenetic diversity of bacteria associated with the marine sponge Rhopaloeides odorabile. Appl. Environ. Microbiol., 67: 434–444.
Xu W X, Peng J, Wang J C, Chen X H, Qian P L. 2001. A novel and simple model for screening of antitumor agents. Chin. J. Antibiot., 1: 15–18.
Yoon B J, You H S, Lee D H. 2011. Aquimarina spongiae sp. nov., isolated from marine sponge Halichondria oshoro. Int. J. Syst. Evol. Microbiol., 61: 417–421.
Zhao J, Yang N, Zeng R Y. 2008. Phylogenetic analysis of type I polyketide synthase and nonribosomal peptide synthetase genes in Antarctic sediment. Extremophiles, 1 2: 97–105.
0
浏览量
3
Downloads
10
CSCD
关联资源
相关文章
相关作者
相关机构

京公网安备11010802024621