胶州湾沉积物可培养细菌的多样性及其抑菌活性
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天津市海洋局蓬莱19-3油田溢油事故生态修复项目(19-3BC2014-03)


Diversity and antimicrobial activities of cultivable bacteria isolated from Jiaozhou Bay
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    摘要:

    [目的] 海洋微生物在活性物质开发方面具有巨大的应用前景。为了研究胶州湾微生物的多样性和抑菌活性,选取胶州湾9个观测站点的沉积物进行了细菌多样性及抑菌活性分析。[方法] 采用YPD和Z2216E培养基分离细菌,通过16S rRNA基因测序对分离菌株进行分类鉴定,继而采用牛津杯法考察分离菌株对7株指示菌的抑菌活性,最后用PCR方法筛选16株代表菌的PKSINRPSCYPPhzEdTGD基因。[结果] 从胶州湾沉积物中共分离出76株细菌,通过对16S rRNA序列分析,将其归为8个科11个属:节杆菌属、考克氏菌属、微球菌属、微杆菌属、假交替单胞菌属、Oceanisphaera、海单胞菌属、葡萄球菌属、芽孢杆菌属、硫胺素芽孢杆菌属和短芽孢杆菌属,其中分离细菌中有34株至少对1种指示菌有抑菌活性。所选取的16株菌均能检测到一种功能基因,且其中5株菌能同时检测到3种以上的功能基因。[结论] 以上研究表明胶州湾海域有丰富的微生物资源,在生物活性次级代谢产物合成上有较大潜力。

    Abstract:

    [Objective] Marine microorganisms have a great potential in producing biologically active secondary metabolites. In order to study the diversity and antimicrobial activity, we explored 9 sediment samples in different observation sites of Jiaozhou bay.[Methods] We used YPD and Z2216E culture medium to isolate bacteria from the sediments; 16S rRNA was sequenced for classification and identification of the isolates. Then, we used Oxford cup method to detect antimicrobial activities of the isolated bacteria against 7 test strains. Lastly, we selected 16 representatives to detect secondary-metabolite biosynthesis genes:PKSI, NRPS, CYP, PhzE, dTGD by PCR specific amplification.[Results] A total of 76 bacterial strains were isolated from Jiaozhou bay; according to the 16S rRNA gene sequence analysis. These strains could be sorted into 11 genera belonging to 8 different families:Aneurinibacillus, Brevibacillus, Microbacterium, Oceanisphae, Bacillus, Marinomonas, Staphylococcus, Kocuria, Arthrobacters, Micrococcus and Pseudoalteromonas. Of them 34 strains showed antimicrobial activity against at least one of the tested strains. All 16 strains had at least one function genes, 5 strains possessed more than three function genes.[Conclusion] Jiaozhou bay area is rich in microbial resources with potential in providing useful secondary metabolites.

    参考文献
    [1] Blair JMA,Webber MA,Baylay AJ,Ogbolu DO,Piddock LJV.Molecular mechanisms of antibiotic resistance.Nature Reviews Microbiology,2015,13(1):42-51.
    [2] Chopra I.The 2012 garrod lecture:discovery of antibacterial drugs in the 21st century.Journal of Antimicrobial Chemotherapy,2013,68(3):496-505.
    [3] Bose U,Hewavitharana AK,Ng YK,Shaw PN,Fuerst JA,Hodson MP.LC-MS-based metabolomics study of marine bacterial secondary metabolite and antibiotic production in Salinispora arenicola.Marine Drugs,2015,13(1):249-266.
    [4] Song YX,Liu GF,Li J,Huang HB,Zhang X,Zhang H,Ju JH.Cytotoxic and antibacterial angucycline-and prodigiosin-analogues from the deep-sea derived Streptomyces sp.SCSIO 11594.Marine Drugs,2015,13(3):1304-1316.
    [5] Phelan RW,Barret M,Cotter PD,O'Connor PM,Chen R,Morrissey JP,Dobson ADW,O'Gara F,Barbosa TM.Subtilomycin:a new lantibiotic from Bacillus subtilis strain MMA7 isolated from the marine sponge haliclona simulans.Marine Drugs,2013,11(6):1878-1898.
    [6] Mathew BP,Nath M.Recent approaches to antifungal therapy for invasive mycoses.ChemMedChem,2009,4(3):310-323.
    [7] Du LC,Lou LL.PKS and NRPS release mechanisms.Natural Product Reports,2010,27(2):255-278.
    [8] McDonald M,Mavrodi DV,Thomashow LS,Floss H.Phenazine biosynthesis in Pseudomonas fluorescens:branchpoint from the primary shikimate biosynthetic pathway and role of phenazine-1,6-dicarboxylic acid.Journal of the American Chemical Society,2001,123(38):9459-9460.
    [9] Oh TJ,Mo SJ,Yoon YJ,Sohng JK.Discovery and molecular engineering of sugar-containing natural product biosynthetic pathways in actinomycetes.Journal of Microbiology and Biotechnology,2007,17(12):1909-1921.
    [10] Stockmann M,Piepersberg W.Gene probes for the detection of 6-deoxyhexose metabolism in secondary metabolite-producing streptomycetes.FEMS Microbiology Letters,1992,90(2):185-190.
    [11] Zhu P,Zheng L,Lin J,Shao JZ,Yan XJ.Screening and characterization of marine bacteria with antibacterial and cytotoxic activities,and existence of PKSI and NRPS genes in bioactive strains.Acta Microbiologica Sinica,2007,47(2):228-234.(in Chinese)朱鹏,郑立,林晶,邵健忠,严小军.抗菌和细胞毒活性海洋细菌的筛选及其次生代谢基因证据.微生物学报,2007,47(2):228-234.
    [12] Schneemann I,Wiese J,Kunz AL,Imhoff JF.Genetic approach for the fast discovery of phenazine producing bacteria.Marine Drugs,2011,9(5):772-789.
    [13] Lee MY,Myeong JS,Park H J,Han K,Kim ES.Isolation and partial characterization of a cryptic polyene gene cluster in Pseudonocardia autotrophica.Journal of Industrial Microbiology and Biotechnology,2006,33(2):84-87.
    [14] Du Y,Li TB,Wang YG,Xia HZ.Identification and functional analysis of dTDP-glucose-4,6-dehydratase gene and its linked gene cluster in an aminoglycoside antibiotics producer of Streptomyces tenebrarius H6.Current Microbiology,2004,49(2):99-107.
    [15] Zhang XY,Han XX,Chen XL,Dang HY,Xie BB,Qin QL,Shi M,Zhou BC,Zhang YZ.Diversity of cultivable protease-producing bacteria in sediments of Jiaozhou bay,China.Frontiers in Microbiology,2015,6:1021.
    [16] Xiong ZQ,Wang JF,Hao YY,Wang Y.Recent advances in the discovery and development of marine microbial natural products.Marine Drugs,2013,11(3):700-717.
    [17] Hornung A,Bertazzo M,Dziarnowski A,Schneider K,WelzelK,Wohlert SE,Holzenkmpfer M,Nicholson GJ,Bechthold A,Süssmuth RD,Vente A,Pelzer S.A genomic screening approach to the structure-guided identification of drug candidates from natural sources.ChemBioChem,2007,8(7):757-766.
    [18] Chen FF,Lin L,Wang L,Tan Y,Zhou HX,Wang YG,Wang Y,He WQ.Distribution of dTDP-glucose-4,6-dehydratase gene and diversity of potential glycosylated natural products in marine sediment-derived bacteria.Applied Microbiology and Biotechnology,2011,90(4):1347-1359.
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王怡婷,张传波,齐麟,贾晓强,卢文玉. 胶州湾沉积物可培养细菌的多样性及其抑菌活性[J]. 微生物学报, 2016, 56(12): 1892-1900

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  • 收稿日期:2016-04-03
  • 最后修改日期:2016-05-24
  • 在线发布日期: 2016-11-29
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