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海洋放线菌胞外多糖发酵工艺及其条件研究 总被引:1,自引:0,他引:1
以具有明显海洋特性的、产胞外免疫活性多糖的链霉菌2305菌株作为发酵菌种,对其胞外多糖的发酵工艺及其条件进行了研究,考察了不同碳源、氮源、水质、培养基初始pH值、发酵温度、通气量等因素对发酵菌种的生物量及胞外多糖产量等的影响,建立和优化了胞外多糖摇瓶发酵培养基配方、发酵工艺及发酵条件,胞外多糖产量达到4.58g/L,转化率达到6.90%。研究了发酵过程中菌体生物量、底物糖残余量、pH值、产物多糖积累量等的动态变化,分析讨论了2305菌株胞外多糖发酵的动力学类型。 相似文献
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紫球藻胞外多糖抗氧化和免疫调节活性的研究 总被引:1,自引:0,他引:1
采用密闭微波法降解紫球藻胞外多糖。通过测定多糖对羟自由基OH·、超氧阴离子O2-·和二苯代苦味酰基自由基DPPH·的清除效果及对小鼠单核-巨噬细胞RAW264.7和淋巴细胞的增殖效果,考察低分子量紫球藻多糖的体外抗氧化活性和免疫调节活性。结果表明,在一定的浓度范围内,降解后的紫球藻多糖对OH·、O2-·和DPPH·的清除能力与浓度呈正相关性,它们的半抑制率IC50分别为0.619,0.114和0.015mg/mL,表明紫球藻胞外多糖具有体外抗氧化活性。溶液浓度在50~200μg/mL的多糖都表现出体外免疫促进作用,与对照组相比,100μg/mL的多糖对巨噬细胞RAW264.7的促进作用最大,其增值指数为1.72。200μg/mL的多糖对脾淋巴细胞的增值指数为2.11。 相似文献
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营养盐水平对四种海洋浮游硅藻胞外多糖产量的影响 总被引:10,自引:0,他引:10
4种海洋浮游硅藻(牟勒氏角毛藻、海链藻、三角褐指藻和新月菱形藻)培养在改进的f/2培养基中,研究了不同氮、磷和硅营养水平对它们胞外多糖产量的影响.结果表明,硅藻胞外多糖的生产和释放具有种间特异性,角毛藻和海链藻胞外多糖的生产和释放主要在静止期,而三角褐指藻和新月菱形藻在指数生长期前期和静止期都能生产和分泌较高的胞外多糖;培养液中低浓度磷减少了4种硅藻在静止期胞外多糖的产量,但增加了角毛藻在生长期前期胞外多糖的产量;氮浓度的降低增加了三角褐指藻在指数生长前期胞外多糖的产量,但减少了其他3种藻类胞外多糖的产量;硅浓度的降低对4种硅藻胞外多糖的产量影响不大,在一定程度上还促进了静止期胞外多糖的生产.本研究表明,营养盐水平对硅藻胞外多糖生产的影响因种类和细胞所处生长期不同而存在着很大的差异. 相似文献
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海洋动植物共附生放线菌抗真菌活性菌株的生态分布 总被引:4,自引:0,他引:4
对分离自台湾海峡厦门海域的鹧鸪菜,海仙人掌等8种海洋动植物共附生放线菌,以4种常见的致病真菌黑曲霉(Aspergillus nige),弯孢霉(Curvularia sp),镰刀菌(Fusarium sp),木霉(Trichoderma sp)作为抗真菌药物的筛选指示菌,进行了抗真菌活性菌株的生态分布研究。结果表明,供测的149株放线菌,19株具有抗真菌活性,占总供测菌株的12.8%;鹧鸪菜共附生放线菌抗真菌活性菌株比例最高,达40.9%;高抗菌株主要分布于鹧鸪菜,海仙人掌和沙菜上,其中以鹧鸪菜最高,占供测菌株的31.8%。 相似文献
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采用苯酚硫酸法和醇沉淀法,从600余株南极微生物中筛选得到10株胞外多糖产量较高的菌株.分子鉴定与系统发育分析表明,9株菌株属于假交替单胞菌属(Pseudoalteromonas),1株属于嗜冷杆菌属(Psych robacter).对10株菌株进行发酵培养,发酵液经醇沉、除蛋白、冷冻干燥后得到粗胞外多糖.其中菌株3-3-1-2的胞外多糖产量达0.6 g/L.对粗多糖产量较高的4株菌所产的胞外多糖进行免疫活性试验,粗胞外多糖20#3在注射3d时,实验组AKP活性比对照组增加了39%,CAT活性比对照组增加了24%,二者均差异显著(P<0.05),注射5d时,ACP活性比对照组增加了20%,差异显著(P<0.05),总超氧化物歧化酶(T-SOD)活性比对照组增加了14%,差异极显著(P<0.01);粗胞外多糖33-1-2在注射3d时,实验组AKP活性比对照组增加了12%,差异不显著(P>0.05),注射5d时,酸性磷酸酶(ACP)活性比对照组增加了24%,过氧化氢酶(CAT)活性比阳性对照组增加了5%,二者均差异显著(P<0.05).研究结果表明,菌株20#3与3-3-12产生的胞外多糖对大菱鲆(Scophthalmus maxoimus)具有显著的免疫促进作用.由此可知,筛选出的极地细菌胞外多糖20#3和3-31-2可显著提高大菱鲆非特异性免疫力,可作为水产饲料添加剂应用于大菱鲆的生产养殖. 相似文献
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Isolation and phylogenetic assignation of actinomycetes in the marine sediments from the Arctic Ocean 总被引:2,自引:0,他引:2
Actinomycetes in five marine sediments collected from the Arctic Ocean at depths of 43 to 3 050 m were cultivated using a variety of media. A total of 61 actinomycete colonies with substrate mycelia only were observed, and no colonies with aerial mycelia were observed under aerobic conditions at 15 ℃. From these colonies, 28 were selected to represent different morphological types.Denaturing gradient gel electrophoresis (DGGE) was used to check the purity of isolates and select representatives for subsequent sequencing. Phylogentic analyses based on nearly full-length 16S ribosomal RNA gene (rDNA) sequences indicated that the actinomycetes isolated were accommodated within genus Rhodococcus of family Nocardiaceae, genus Dietzia of family Dietziaceae,genera Janibacter and Terrabacter of family Instrasporangiaceae and genera Kocuria and Arthrobacter of family Micrococcaceae. One of the strains (P27-24) from the deep-sea sediment at depth of 3 050 m was found to be identical in 16S rDNA sequence(1474/1474)with the radiation-resistant Kocuria rosea ATCC 187T isolated from air. More than halfofthe isolates showed the similarities ranging from 99.5% to 99.9% in 16S rDNA sequence to dibenzofran-degrading, butyl 2-ethylhexanoate-hydrolysising and nitrile-metabolizing actinomycetes. All the strains isolated were psychrotolerant bacteria and grew better on the media prepared with natural seawater than on the media prepared with deionized water. Three of them (Dietzia sp. P27-10, Rhodococcus sp. S11-3 and Rhodococcus sp.P11-5)had an obligate growth requirement for salt, confirming that these strains are indigenous marine actinomycetes. 相似文献
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In exploring new sources for economically important products, marine environment draws particular attention because of its remarkable diversity and extreme conditions; it is known to produce metabolic products of great value. It represents untapped source for the discovery of novel secondary metabolites with varying potential such as antibiotic, anti-tumor, antifouling and cytotoxic properties. Marine actinomycetes distributed throughout the marine environment from shallow to deep sea sediments have proved to be a finest source for this discovery. Secondary metabolites derived from marine actinomycetes have proved their worth in industries based on the research on their properties and wide range applications. Spotlight of the review is range of marine based actinomycetes products and significant research in this field. This shows the capability of marine actinomycetes as bioactive metabolite producers. Additionally, the present review addresses some effective and novel approaches of procuring marine microbial compounds utilizing the latest screening strategies of drug discovery from which traditional resources such as marine actinobacteria has decreased due to declining yields. The aim is in the context of promoting fruitful and profitable results in the near future. The recent surfacing of new technologies for bioprospection of marine actinomycetes are very promising, resulting in high quality value added products, and will be de? ning a new era for bioactive compounds with medical and biotechnological applications. 相似文献
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产碱性纤维素酶海洋细菌的筛选、鉴定及酶学性质研究 总被引:3,自引:1,他引:3
用CMC平板筛选方法,从青岛近海海域海水中分离出一株产碱性纤维素酶的海洋菌株QM11,经16S rDNA鉴定,该菌株为Cytophaga fucicola.对该菌的生物学特性研究表明,其最适生长温度为27℃,生长温度范围为4~48℃,为耐冷菌;在pH7.0~8.0、含3.0%NaC1的培养基条件下,最适宜菌株生长和产酶;QM11所产碱性纤维素酶最适反应温度为40℃,最适反应pH为9.0,在碱性条件下具有较高的酶活性和较好的稳定性.Mn2+、Fe3+对酶反应具有促进作用,Cu2+、Pb2+对酶反应具有抑制作用. 相似文献
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采用稀释涂板法研究了南麂岛海域沉积物中海洋放线菌的分离技术,分析了真空干燥处理、热处理、海水浓度、培养基种类等因素对分离效果的影响;首次将羧甲基纤维素钠(CMC)溶液应用于海洋沉积物样品的预处理,探讨了不同浓度的CMC对海洋沉积物样品中放线菌分离结果的影响。结果表明:海洋沉积物经干燥处理、50℃热处理20 min均能有效地减少细菌数量,利于海洋沉积物中放线菌的分离;60%的海水配制的培养基对海洋放线菌的分离效果优于纯海水所配培养基,并且培养基中添加海泥浸出液能有效地增加海洋放线菌的出菌率;以质量浓度为2 g/L的CMC为分散剂时,不仅能良好地分散沉积物样品中的放线菌孢子,而且能明显地增加海洋放线菌的检出量及稀有放线菌的数量。 相似文献
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群体感应抑制剂(Quorum Sensing Inhibitors, QSIs)可以通过干扰群体感应(Quorum Sensing, QS)而有效降低病菌的感染性和毒力, 并且不会胁迫致病菌使其产生耐药性, 是具有前景的抗生素替代品。海洋微生物是新型QSIs的潜在来源。本研究利用紫色杆菌(Chromobacterium violaceum 026, CV026)模型评价QS抑制活性, 在来源于南海中西部和印度洋深海沉积物样品的放线菌中筛选QS抑制活性菌株, 并且根据形态学特征和16S rRNA基因序列鉴定活性菌株。通过筛选获得了菌株SCSIO 53717, 其提取物在CV026模型中能够显著降低指示菌株的紫色菌素产量, 并且在0~1000mg·mL-1的有效浓度范围内不影响紫色杆菌的生长。菌株SCSIO 53717被鉴定为Kocuria属, 是首次报道的具有QS抑制活性的Kocuria属菌株, 因而具有进一步深入研究的价值。 相似文献
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探究了南大西洋深海沉积物中可培养放线菌的多样性,筛选药源活性次级代谢产物产生菌,为后续资源开发奠定基础.采用3种预处理方法及8种选择性培养基对南大西洋3个深海沉积物样品中的放线菌菌株进行选择性分离鉴定;利用兼并引物扩增法,选取代表菌株进行聚酮合酶(PKSⅠ、PKSⅡ)基因和非核糖体多肽合成酶(NRPS)基因的检测;以4株细菌为指示菌检测代表菌株的抑菌活性.共分离得到132株放线菌纯菌株,分布于放线菌亚纲的6个目、13个科、19个属中,其中有5个属为较新或较稀有种属,有2株为潜在新种.34株化合物合成基因检测菌中PKSⅠ基因、PKSⅡ基因呈阳性的比率均为17.64%,NRPS基因呈阳性的则为52.94%.抗枯草芽孢杆菌(Bacillus subtilis)和抗副溶血性弧菌(Vibrio parahaemolyticus)的菌株分别有47.06%和7.82%.南大西洋深海沉积物中放线菌资源丰富,存在较多潜在新分类单元,筛选到的活性菌株可用于后续药源活性次级代谢产物的分离. 相似文献