海南西海岸四种真红树根系土壤放线菌物种多样性及其延缓衰老活性初筛

为更好地开发利用海洋微生物资源积累丰富的放线菌菌种,该文以海南西海岸潮间带区域四种真红树根系土壤为研究对象,分析了红树林根系放线菌物种多样性组成及其代谢产物活性。该研究以9种不同培养基为分离介质,采用纯培养方法和三区划线法分离纯化菌株,结合放线菌形态学特征及其16S rRNA基因序列结果开展多样性分析。放线菌发酵液经乙酸乙酯萃取,利用秀丽隐杆线虫(Caenorhabditis elegans)测试其延缓衰老活性。结果表明:(1)共分离获得22株放线菌,隶属于4目7科9属,其中链霉菌属(Streptomyces)为优势菌群,并初步确认IMDGX 6012、IMDGX 6028、IMDGX 6118、IMDGX 6326、IMDGX 6119 5株放线菌可能为潜在的新物种。(2)发酵产物延缓衰老研究结果表明,8株放线菌的代谢产物可显著延长线虫寿命(P0.05);其中,IMDGX 6028和IMDGX 6118作为拟无枝酸菌属(Amycolatopsis)和短小杆菌属(Curtobacterium)的潜在新物种,具有极显著延缓衰老活性(P 0. 01),与空白组比较,可分别延长线虫寿命的22.2%和26.6%。综上结果表明海南西海岸真红树根系土壤具有丰富的可培养放线菌资源,具有发现放线菌新物种和延缓衰老活性菌株的潜力。     

海南西海岸真红树内生细菌多样性及其延缓衰老活性研究

该文设计9种分离培养基,采用稀释涂布法从14份真红树植物的46份组织样品中分离纯化内生细菌。并基于菌株形态学特征和16S rRNA基因序列确定分离菌株的种属及分析其物种多样性,采用秀丽隐杆线虫模型筛选菌株延缓衰老活性。结果表明:(1)通过基因序列去重复后从46份真红树植物组织样品中获得32株海洋细菌,基于菌株16S rRNA基因序列信息分析,覆盖12科17属,其中芽孢杆菌属(Bacillus)为优势菌属,并获得1株疑似橙单胞菌属(Aurantimonas)新种,16S rRNA基因序列相似性低于97%;(2)经过秀丽隐杆线虫粗筛发现3株海洋细菌具有显著延缓线虫衰老的活性(P0.05)。以上结果表明海南西海岸真红树内生细菌具有物种多样性,部分菌株具有延缓线虫衰老活性。     

海南西海岸真红树内生放线菌多样性及其延缓衰老活性初筛

为了发掘红树林内生放线菌资源和进行新型海洋药物研究,该文选择海南西海岸14种真红树的根、茎、叶、花、胚轴为研究对象,采用9种不同分离培养基[改良的高氏培养基(AGG)、海藻糖-天冬酰胺培养基(M4)、海藻糖-脯氨酸培养基(M5)、改良ISP5培养基(M7)、精氨酸-天冬酰胺培养基(M9)、改良淀粉-水解酪素培养基(M10)、酪氨酸-天冬酰胺培养基(P7)、燕麦培养基(P3)、棉籽糖-组氨酸培养基(M11)],结合稀释涂布法和三线划线法从真红树组织中分离菌株,基于菌株16S rRNA基因序列信息等分子生物学鉴定方法对获得的海洋放线菌进行多样性分析,并使用模式生物秀丽隐杆线虫对所得内生放线菌的延缓衰老活性进行研究。结果表明:(1)从46份真红树组织中共获得24株放线菌,隶属于7科11属,其中9株菌株为链霉菌属(Streptomyces),且IMDGX 6270、IMDGX 6137和IMDGX 6173为3株疑似潜在新菌株。(2)秀丽隐杆线虫模型筛选发现4株放线菌(IMDGX 6157、IMDGX 6182、IMDGX 6248、IMDGX 6360)具有延缓衰老的活性,与空白组比较,生存时间分别延长17.16%、28.11%、29.05%、27.10%。综上结果说明海南西海岸区域真红树植物中可能含有较丰富的放线菌资源,能够为延缓衰老药物的研发提供新来源。     

根结线虫放线菌及其生物防治活性研究

从感染植物根部的根结线虫卵和雌虫中,分离得到放线菌20株。形态、细胞壁氨基酸组分和16S rRNA基因序列分析表明:分离菌株分属于链霉菌属(Streptomyces)、诺卡氏菌属(Nocardia)和假诺卡氏菌属(Pseudonocardia),其中链霉菌占80.0%。分离菌株对根结线虫Meloidogynespp.卵的平均寄生率、卵的孵化率、幼虫死亡率分别为54.1%、40.4%和26.2%。根据体外测试的结果,选择具有高致病力的3株链霉菌(1-17,2-6,9-47)和1株诺卡氏菌(5-1)进行温室番茄防效测试,其生防效率分别为31.4%、37.7%、56.4%和42.4%。     

塔里木盆地荒漠盐碱生境土壤放线菌的初步研究

采用常规方法研究了新疆塔里木盆地荒漠盐碱生境土壤放线菌区系、放线菌的耐盐、碱性及对植物病原真菌的拮抗性。结果表明:土壤放线菌区系较单一,仅分离到链霉菌属和拟诺卡氏菌属,其中以链霉菌属为主(98.57%),链霉菌可分10个类群,以白孢类群为优势类群。土壤含盐量愈高,链霉菌组成愈简单。放线菌的最适生长盐浓度多集中在6%~8%,最适生长pH集中在7~8。24株供试放线菌中,有4株中度嗜盐放线菌对供试靶标菌有拮抗性,占供试菌的16.67%。     

三江源地区不同退化程度草地的土壤放线菌区系

用不同分离方法,对三江源地区不同退化程度草地土壤放线菌的数量和多样性进行了比较.从5份土样中共分离放线茵178株,根据表型特征和16S rRNA基因序列分析,分别归入7个已知属:小单孢菌属(Micromonospora)、原小单孢菌属(Promicromonospora)、诺卡氏菌属(Nocardia)、假诺卡氏菌属(Pseudonocardia)、游动放线菌属(Actinoplanes)、韩国生工茵属(Kribbella)和链霉菌属(Streptomyces).其中链霉菌属分离菌株可归入7个表型类群.发现轻度退化高寒草原的土壤放线菌数量,丰度和多样性高于重度退化高寒草原;针茅高寒草原的土壤放线菌数量和多样性高于蒿草高寒草甸,而其中链霉菌的种类低于后者.表明高寒草地的退化程度与其中土壤放线茵的数量和多样性呈负相关.     

从红树植物根际土壤选择性分离小双孢菌

从海南文昌采集23种红树植物的根际土壤, 采用GA、HV作为选择性分离培养基, 添加复合维生素、放线菌酮、制霉菌素和重铬酸钾, 结合适当的预处理: 干热120°C 60 min或干热100°C 60 min及1% 氯胺-T处理30 min, 平板稀释涂布法(10-1、10-2、10-3)分离其中的小双孢菌。共分离得到199株放线菌, 通过培养特征及显微形态观察, 发现其中有链霉菌147株、非链霉菌52株。选择7株链霉菌和28株非链霉菌进行了16S rRNA基因序列分析, 结果显示19株菌属于小双孢菌属, 7株属于链霉菌属, 4株属于野野村菌属, 2株属于小单孢菌属, 1株属于链孢囊菌属, 1株属于阿萨诺氏菌属, 1株属于小单孢菌科。结果表明红树林根际土壤中蕴含着丰富的小双孢菌资源。     

广西沿海地区红树林根系土壤中放线菌的分离与鉴定

本研究通过分离纯培养,从广西北海及防城港红树林根系土壤中分离出放线菌并提取其总DNA,用放线菌通用引物对获得菌株的16S rDNA进行PCR扩增,对获得的扩增产物进行DNA序列测定及菌株鉴定.研究结果表明,从红树林根系土壤样品中分离出15株典型放线菌菌株.16S rDNA测序比对鉴定结果显示,15株典型放线菌菌株中有12株属于链霉菌属(Streptomyces),是常见菌属;3株属于拟诺卡氏菌属(Nocardiopsis),为稀有放线菌.本研究分离纯化获得15株典型放线菌,初步揭示了广西沿海地区红树林土壤中放线菌的多样性.     

山西运城盐湖放线菌区系研究

从山西运城盐湖分离到中、高温嗜碱或耐碱放线菌120株,对其进行了分类鉴定。根据形态和分类特征（细胞壁化学成分）,分别归入拟诺卡氏菌属（Nocardiopsis）、诺卡氏菌科（Nocediaceae）、小多孢菌属（Micromonospora）、马杜拉放线菌属（Actinomadura）及链霉菌属（Streptomyces）,并将链霉菌归入了11个类群。     

热带药用植物根际放线菌的分离、鉴定及生物活性分析

从海南热带植物园采集12种药用植物的根际土样,采用选择性分离方法,分离得到400株根际放线菌。使用5种活性筛选模型对分离菌株进行生物活性评价,154株放线菌在一个或多个活性筛选模型中显示为阳性,菌株初筛阳性率达38.5%;根据菌株形态特征并结合代谢产物的生物活性,从中挑选出28株菌进行16S rRNA基因序列分析,发现其分属于链霉菌属、诺卡氏菌属、小单孢菌属和野野村菌属。     

北部湾徐闻海域红树内生细菌物种多样性及其杀线虫活性研究

为发掘红树植物内生细菌资源和寻找新型微生物杀虫剂,该研究从北部湾徐闻海域采集7种红树植物共16份样品,设计10种分离培养基,使用稀释涂布法分析红树植物内生细菌的分布特征,通过16S rRNA分子生物学方法对内生细菌进行多样性分析,并利用秀丽隐杆线虫模型,通过杀线虫活性实验测试内生细菌乙酸乙酯提取物的杀线虫活性。结果表明:(1)从16份红树植物各组织器官中获得33株内生细菌,分布于19个科23个属。其中,芽孢杆菌属(Bacillus)为优势菌属,并发现了10株潜在的新种或新属。(2)筛选到具有显著杀线虫活性的菌株IMDGX 4725和IMDGX 4744,半数致死浓度(LC_(50))分别为61.58、100.89mg·mL~(-1)。研究结果证实了徐闻海域红树具有多样性丰富的内生细菌,同时部分细菌具有较强的杀线虫活性,具有发现新型微生物杀虫剂的潜力。     

Investigation of anti-inflammatory and toxicity effects of mangrove-derived Streptomyces rochei strain VITGAP173

Mangrove ecosystems generate the major biodiversity hotspots of actinobacteria. Among the actinobacteria, Streptomyces species are the prolific producers of bioactive natural products. In this study, with research efforts to discover biopotential compounds from marine actinobacteria, 41 actinobacterial strains were isolated from sediment soil sample of Indian mangrove regions. The phylogeny prediction using the 16S rRNA gene sequences revealed that the isolates were related to Streptomyces. Isolates were further screened based on a two-step process wherein the first step, around nine strains, unveiled the presence of type 1 polyketide synthase gene and dTDP-glucose 4,6-dehydratase gene through polymerase chain reaction. As the second step of the screening process, cell viability assay was performed in RAW264.7 cells to assess the toxicity of extracts. Among all the isolates, Streptomyces rochei strain VITGAP173 was subjected to further analysis. To explore the bioactivities, the organic solvent extraction method was utilized to extract the broth culture of VITGAP173. Inhibition of nitric oxide and cyclooxygenase enzymes upon lipopolysaccharide-induced inflammation were utilized to evaluate the anti-inflammatory efficacy, and the results showed the potency of VITGAP173 in a dose-dependent manner. The extract significantly suppressed the messenger RNA levels of the inflammatory mediators such as tumor necrosis factor-α and interleukin-6 induced by lipopolysaccharide in RAW264.7 macrophages. The presence of several chemical constituents was identified through gas chromatography-mass spectrometry analysis of VITGAP173 extract. To achieve the toxicity analysis, oral administration of VITGAP173 extract in Wistar albino rats was carried out to investigate the biochemical parameters, histopathology which revealed its nontoxic nature.     

Streptomyces associated with a marine sponge Haliclona sp.; biosynthetic genes for secondary metabolites and products

Terrestrial actinobacteria have served as a primary source of bioactive compounds; however, a rapid decrease in the discovery of new compounds strongly necessitates new investigational approaches. One approach is the screening of actinobacteria from marine habitats, especially the members of the genus Streptomyces. Presence of this genus in a marine sponge, Haliclona sp., was investigated using culture‐dependent and ‐independent techniques. 16S rRNA gene clone library analysis showed the presence of diverse Streptomyces in the sponge sample. In addition to the dominant genus Streptomyces, members of six different genera were isolated using four different media. Five phylogenetically new strains, each representing a novel species in the genus Streptomyces were also isolated. Polyphasic study suggesting the classification of two of these strains as novel species is presented. Searching the strains for the production of novel compounds and the presence of biosynthetic genes for secondary metabolites revealed seven novel compounds and biosynthetic genes with unique sequences. In these compounds, JBIR‐43 exhibited cytotoxic activity against cancer cell lines. JBIR‐34 and ‐35 were particularly interesting because of their unique chemical skeleton. To our knowledge, this is the first comprehensive study detailing the isolation of actinobacteria from a marine sponge and novel secondary metabolites from these strains.     

Culturable Actinobacteria from the Marine Sponge Hymeniacidon perleve: Isolation and Phylogenetic Diversity by 16S rRNA gene-RFLP Analysis

A total of 106 actinobacteria associated with the marine sponge Hymeniacidon perleve collected from the Yellow Sea, China were isolated using eight different media. The number of species and genera of actinobacteria recovered from the different media varied significantly, underlining the importance of optimizing the isolation conditions. The phylogenetic diversity of the actinobacteria isolates was assessed using 16S rRNA gene amplification–restriction fragment length polymorphism (RFLP) analysis of the 106 strains with different morphologies. The RFLP fingerprinting of selected strains by HhaI-digestion of the 16S rRNA genes resulted in 11 different patterns. The HhaI-RFLP analysis gave good resolution for the identification of the actinobacteria isolates at the genus level. A phylogenetic analysis using 16S rRNA gene sequences revealed that the isolates belonged to seven genera of culturable actinobacteria including Actinoalloteichus, Micromonospora, Nocardia, Nocardiopsis, Pseudonocardia, Rhodococcus, and Streptomyces. The dominant genus was Streptomyces, which represented 74% of the isolates. Three of the strains identified are candidates for new species.     

定殖植物根内和根围放线菌的分离鉴定及其体外抑菌促生效应

【目的】旨在分离、筛选并鉴定体外具抑菌促生作用的定殖于植物根内和根围的放线菌,以期丰富放线菌种质资源,为研制植物病害生防菌剂提供技术依据。【方法】采用稀释涂布平板法分离盐碱地、湿地、工业污染土壤中优势植物根内及其根围中的放线菌;通过平板对峙试验筛选具有抑菌效应的菌株,进而采用Salkowski比色法、CAS平板检测法和无氮源培养法进一步检测抑菌菌株的促生作用;通过形态观测、生理生化特性检测及16SrRNA基因序列分析鉴定菌种。【结果】共分离到链霉菌属(Streptomyces)、诺卡氏菌属(Nocardia)和小单孢菌属(Micromonospora) 3属共283株定殖于植物根内和根围的放线菌,3个采样地中湿地数量最多,均为根围土根内;其中链霉菌属占总数的77%,可分为10个类群。经筛选获得7株抑菌活性和促生效应较强的菌株,其中菌株H6-1抑菌效应最大,其无菌发酵液对尖孢镰刀菌(Fusariumoxysporum)、禾谷镰刀菌(Fusariumgraminearum)、灰葡萄孢菌(Botrytis cinerea)、立枯丝核菌(Rhizoctoniasolani)、轮纹大茎点霉(Macrophomakawatsukai)和瓜类炭疽菌(Colletotrichumorbiculare)的抑制率分别为32.3%、42.6%、48%、72.2%、58.1%和60.5%;而D11-4菌株的促生作用最强,能产吲哚乙酸(22.3 mg/L)、产铁载体(晕圈直径25.2 mm)和固氮。经鉴定这7株放线菌是吸水链霉菌变种(Streptomyces angustmyceticus) H4-6、娄彻氏链霉菌(Streptomyces rochei) S2-2、浑圆链霉菌(Streptomycesglobosus)H6-1、(Streptomycesiakyrus)GD8-4、波卓链霉菌(Streptomyces bottropensis) GH8-6、(Streptomyces paradoxus) H8-2和(Streptomyces coralus) D11-4。【结论】三个生境中定殖于植物根内和根围的放线菌类群丰富且所筛选获得的7株放线菌具有生防潜力,值得进一步研发。     

Marine <Emphasis Type="Italic">Streptomyces</Emphasis> as a novel source of bioactive substances

Marine actinobacteria are the most economically as well as biotechnologically valuable prokaryotes. Representative genera of marine actinobacteria include Actinomadura, Aeromicrobium, Dietzia, Gordonia, Marinophilus, Micromonospora, Nonomuraea, Rhodococcus, Saccharomonospora, Saccharopolyspora, Salinispora, Streptomyces, Solwaraspora, Williamsia, Verrucosispora and several others. Among the genera of marine actinobacteria, the genus Streptomyces is represented in nature by the largest number of species and varieties, which differ greatly in their morphology, physiology, and biochemical activities. Marine Streptomyces occur in different biological sources such as fishes, molluscs, sponges, seaweeds and mangroves, besides seawater and sediments. In this review an evaluation is made on the present state of research on marine Streptomyces and its perspectives. The highlights include the production of metabolites such as antibiotics, anticancer compounds, enzymes, enzyme inhibitors and pigments by marine Streptomyces and their application as single cell protein and as probiotics in aquaculture. The marine environment contains a wide range of distinct Streptomyces that are not present in the terrestrial environment. With increasing advancement in science and technology, there would be greater demands in future for new bioactive compounds synthesised by Streptomyces from various marine sources.     

Production and Purification of a Bioactive Substance Inhibiting Multiple Drug Resistant Bacteria and Human Leukemia Cells from a Salt-Tolerant Marine Actinobacterium sp. Isolated from the Bay of Bengal

Four marine actinobacteria tolerant to 200 g NaCl l⁻¹ were screened for antibacterial activity against eight patient-derived multiple drug resistant (MDR) bacteria. The active compound (MW 300.2, predicted molecular formula C₂₀H₂₈O₂) from an actinobacterium, was inhibitory to three Gram-positive and three Gram-negative MDR bacteria, seven non-clinical Gram-positive, four Gram-negative bacteria and five fungi (MIC: 3.5–4.0 µg ml⁻¹). Also, 54% of human leukemia (HL-60) cells were killed by the compound at 0.05 µg ml⁻¹. Bioreactor production demonstrated unusual primary metabolite kinetics. Molecular phylogenetic analysis showed this typical intertidal inhabitant to be a member of the Streptomyces genus and distinct from other salt-tolerant actinobacteria. As no compound was found to match the properties in several electronic databases, our screening strategy should increase the possibility of discovering bioactive molecules from rare actinobacteria.     

Research on marine actinobacteria in India

Marine actinobacteriology is one of the major emerging areas of research in tropics. Marine actinobacteria occur on the sediments and in water and also other biomass (mangrove) and substrates (animal). These organisms are gaining importance not only for their taxonomic and ecological perspectives, but also for their unique metabolites and enzymes. Many earlier studies on these organisms were confined only to the temperate regions. In tropical environment, investigations on them have gained importance only in the last two decades. So far, from the Indian peninsula, 41 species of actinobacteria belonging to 8 genera have been recorded. The genus, Streptomyces of marine origin has been more frequently recorded. Of 9 maritime states of India, only 4 have been extensively covered for the study of marine actinobacteria. Most of the studies conducted pertain to isolation, identification and maintenance of these organisms in different culture media. Further, attention has been focused on studying their antagonistic properties against different pathogens. Their biotechnological potentials are yet to be fully explored.