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1.
异形胞分化相关基因在点形念珠藻厚壁孢子中的转录表达   总被引:1,自引:0,他引:1  
点形念珠藻(Nostoc punctiforme)ATCC29133是一种丝状固氮蓝藻,能分化产生异形胞、厚壁孢子、藻殖段等细胞类型。异形胞是一种提供微氧条件以进行固氮作用的特化细胞,厚壁孢子是在逆境下产生的能耐受干旱、冰冻等恶劣环境的细胞1。与异形胞相似,厚壁孢子的外被也具有多糖和糖脂成分2,3。厚壁孢子在某些蓝藻藻丝    相似文献   

2.
在实验室条件下, 首次发现了带形蜈蚣藻(Grateloupia turuturu)盘状体产生的丝状体能够形成孢子, 暂命名为“盘丝体孢子”。研究详细观察了该盘丝体孢子的形成过程, 并探讨了不同温度6、12、16、20、24和30℃及不同光照强度10、30、45、60、90和120 μmol/(m2·s)对盘丝体孢子放散的影响。结果表明: (1) 带形蜈蚣藻雌配子体的囊果释放果孢子, 果孢子发育形成盘状体, 盘状体经过诱导再生出单列细胞的丝状体, 丝状体形成多室孢子囊, 并放散出大量盘丝体孢子; (2) 温度和光照强度均对丝状体中盘丝体孢子的放散产生显著影响。在温度为16℃、光照强度为60 μmol/(m2·s)时盘丝体孢子放散量有最大值; (3) 在温度低于12℃或高于24℃时, 盘丝体孢子的放散受到影响, 数量明显减少; (4) 在光照强度低于30 μmol/(m2·s)或高于90 μmol/(m2·s)时, 盘丝体孢子的放散明显受到抑制。研究结果补充了带形蜈蚣藻无性繁殖过程, 为其种质保存、人工育苗及养殖提供更为丰富的理论依据, 为探讨带形蜈蚣藻的起源与演化提供新思路。  相似文献   

3.
丝状体蓝藻藻殖段的分化及其调节机制   总被引:1,自引:0,他引:1  
钟泽璞  施定基 《植物学报》2000,17(3):204-210
本文介绍了丝状体蓝藻(亦称蓝细菌) 的藻殖段的分化及其调节机制。藻殖段与正常藻丝体的区别在于细胞形状、细胞内存有气囊和可移动的短而直的藻丝链等。本文对许多环境因子包括光和营养因素等促进或抑制藻殖段的分化进行了讨论;还介绍了念珠藻(Nostoc) ,单歧藻(Tolypothrix) 和眉藻(Calothrix)所具有复杂的细胞发育过程,即具气囊又可移动的藻殖段分化,异形胞分化以及营养细胞的补偿性色适应。这三种细胞类型的适应形成取决于两种不同的光受体系统。藻殖段和异形胞两者的分化可能取决于光合电子传递链;而营养细胞的补偿性色适应则受光敏色素的调节。此外,谷酰胺合成酶合成和活性调节的PII蛋白,在协同藻殖段分化、异形胞分化及营养细胞的补偿色适应中起重要作用。由于蓝藻藻殖段分化及其调节机制是一个新的研究领域,关于它的知识尚不完整,亟待人们加强研究。  相似文献   

4.
均匀设计法优化发菜细胞悬浮培养条件   总被引:2,自引:0,他引:2  
通过摇瓶发酵实验研究了培养温度、光照强度等培养条件对发菜细胞悬浮培养生物量和代谢产物发菜多糖累积的影响,通过均匀设计试验对培养条件进行了优化。结果表明:在培养温度24℃、培养基初始pH8.0、光照强度60μmol/(m2.s)、转速150r/min的条件下培养20d,发菜细胞生物量(细胞质量浓度)达到1.34g/L,胞外多糖产量达到208.32mg/L;与优化前相比,发菜细胞生物量和胞外多糖产量分别提高27.3%、111.17%。  相似文献   

5.
丝状体蓝藻藻殖段的分化及其调节机制   总被引:4,自引:0,他引:4  
本文介绍了丝状体蓝藻(亦称蓝细菌)的藻殖段的分化及其调节机制。藻殖段与正常藻丝体的区别在于细胞开状、细胞内存有气囊和可移动的短而真的藻丝链等。本文对许多环境因子包括光和营养因素等促进或抑制藻殖段的分化进行一讨论;还介绍了含球藻(Nostoc),单歧藻(Tolypothrix)和眉藻(Calothrix)所具有复杂的细胞发育过程,即具气囊又可移动的藻殖段分化,异形胞分化以及营养细胞的被偿性色适应。这  相似文献   

6.
发状念珠藻藻殖段的分化及其光合特性的研究   总被引:6,自引:0,他引:6  
发状念珠藻 (NostocflagelliformeBorn .etFlah .)存在着两个重要而明显的个体发育阶段 ,即营养藻丝体和藻殖段。采用弱光 (铺垫砂粒遮光 ) ,红光或在白光下向培养基中加入DCMU (3,4_dichlorophenyl_1,1_dimethylurea)等方法 ,可促进营养藻丝体转变成藻殖段。用可见光吸收光谱、低温荧光发射光谱和光合放氧活性表示发状念珠藻藻丝体与藻殖段的光合特性 ,表明营养藻丝体和藻殖段的可见光吸收光谱和色素含量差别不大。而两者在不同光强范围 (110~ 12 0 0 μmol·m-2 ·s-1)和不同温度 (15~ 45℃ )下的光合放氧活性 ,表明发状念珠藻的藻殖段比营养藻丝体可能更适合在低光强下和较高的温度下生长。从荧光发射光谱可以看出 ,在光合能量传递中营养藻丝体比藻殖段在两个光系统之间的光能分配上更加均衡 ;但是藻殖段中藻胆体吸收光能向两个光系统的传递比营养藻丝体的更加有效。可以认为藻殖段的形成对光合作用的结构与功能产生影响。  相似文献   

7.
钝顶螺旋藻在不同光照条件下的放氧特性   总被引:1,自引:0,他引:1  
钝顶螺旋藻在持续照光和中等频率 (0.01~20 Hz) 的光/暗交替照光下的放氧特性对光生物反应器的设计和操作具有重要意义。构建了一套可实现光/暗交替的光生物反应器系统对此进行研究,结果显示:根据与放氧速率的关系,可以将光强分为4个区:光限制区 (0~335 μmol/(m2·s)),过渡区 (335~875 μmol/(m2·s)),光饱和区 (875~2 775 μmol/(m2·s)) 以及光抑制区 (2 775 μmol/(m2·s)以上)。提高光/暗频率能否提高微藻光合速率取决于所采用的光强和  相似文献   

8.
食用蓝藻——地木耳的开发   总被引:1,自引:0,他引:1  
地木耳隶属原核生物界、蓝藻门、念珠藻属,是植物界最原始的类群之一,因其形似木耳的胶质片状而得名。显微镜下的地木耳是由许多丝状体无规则地集合于一个公共胶鞘中。细胞圆形,排成一列,如念珠串的丝状体。丝状体中有一些比营养细胞略大的异形胞,将丝状体分成许多藻殖段,  相似文献   

9.
以丝状绿藻枝鞘藻(Oedocladium sp.)为实验材料,研究在100、300μmol·m-2·s-1和双侧300μmol·m-2·s-13种光强以及1、3、9、18 mmol/L 4种初始氮浓度下,两步法培养(第12 d时实验组分别更换为无氮培养基及加盐培养基)对枝鞘藻生长、油脂和虾青素积累的影响。结果显示:枝鞘藻最大生物量在双侧300μmol·m-2·s-1光强,18 mmol/L初始氮浓度更换为无氮培养基的条件下达到,为9.61 g/L;最高虾青素含量和最高油脂含量在双侧300μmol·m-2·s-1光强,3 mmol/L初始氮浓度更换为加盐培养基条件下达到,分别达到干重的1.62%和51.19%。研究结果表明高光条件有利于枝鞘藻的生长,双侧高光条件下低氮浓度更换为加盐培养基最有利于枝鞘藻虾青素和油脂的积累。  相似文献   

10.
温、光、盐对硅藻STR01生长、总脂、脂肪酸的影响   总被引:1,自引:0,他引:1  
为了优化新分离STR01的生态培养条件, 采用单因子试验和正交试验研究了不同温度、光照强度、盐度和温、光、盐三因素三水平对该藻的生长、总脂和脂肪酸组成影响。结果表明: 温、光、盐对STR01的生长、总脂和脂肪酸组成影响显著(P<0.05)。生长的适宜温度为15—35℃, 最适25—30℃(K值达0.679—0.682), 总脂含量积累的最适温度是25℃(总脂可达17.23%), 温度20℃时有利于该藻PUFA的积累, 可达34.23%。STR01生长的适宜光照强度为40—120 μmol/(m2·s), 最适光强为60 μmol/(m2·s), 光照强度40 μmol/(m2·s)有利于该藻的PUFA积累, 可达34.29%。STR01生长的适宜盐度为10—35, 最适盐度25, 盐度25时PUFA含量较高(43.42%)。正交试验结果表明温度对STR01的平均相对生长速率和总脂含量影响显著, 生长的最优组合: 温度30℃、光照强度60 μmol/(m2·s)、盐度25, 该组合下的生长速率达0.756; 总脂含量积累的最优组合: 温度30℃、光照强度60 μmol/(m2·s)、盐度20, 该组合下的总脂含量为20.00%。PUFA的最优组合: 温度25℃、光照强度60 μmol/(m2·s)、盐度20, 该组合下PUFA的含量为35.37%。综上所述: 该藻生长迅速, 总脂含量较高, PUFA丰富, 是一种可开发利用的耐高温浮游硅藻。  相似文献   

11.
内蒙古四子王旗地区发菜的分布   总被引:12,自引:0,他引:12       下载免费PDF全文
本文论述了内蒙古四子王旗地区发菜的分布和生态特性。本区发菜由南至北随年平均降水量的减少和海拔高度的降低而增多。在南部典型草原区和中部荒漠草原区发菜呈零星分布;在北部以珍珠柴、红沙为建群种或优势种的小半灌木荒漠区发菜集中分布。发菜对干旱的环境条件适应能力极强,具有耐干旱高温、耐盐碱贫瘠、可以有效地利用低光强的弱光,但不耐长期水湿的生态特性。钙元素和发菜生长关系密切,钙质土是发菜生长和分布的土壤条件。最后,对保护和开发利用野生发菜资源,提出了一些看法。  相似文献   

12.
The terrestrial cyanobacterium Nostoc flagelliforme Berk. et M. A. Curtis has been a popular food and herbal ingredient for hundreds of years. To meet great market demand and protect the local ecosystem, for decades researchers have tried to cultivate N. flagelliforme but have failed to get macroscopic filamentous thalli. In this study, single trichomes with 50 to 200 vegetative cells were induced from free-living cells by low light and used to investigate the morphogenesis of N. flagelliforme under low UV-B radiation and periodic desiccation. Low-fluence-rate UV-B (0.1 W m(-2)) did not inhibit trichome growth; however, it significantly increased the synthesis of extracellular polysaccharides and mycosporine-like amino acids and promoted sheath formation outside the trichomes. Under low UV-B radiation, single trichomes developed into filamentous thalli more than 1 cm long after 28 days of cultivation, most of which grew separately in liquid BG11 medium. With periodic desiccation treatment, the single trichomes formed flat or banded thalli that grew up to 2 cm long after 3 months on solid BG11 medium. When trichomes were cultivated on solid BG11 medium with alternate treatments of low UV-B and periodic desiccation, dark and scraggly filamentous thalli that grew up to about 3 cm in length after 40 days were obtained. In addition, the cultivation of trichomes on nitrogen-deficient solid BG11 medium (BG11(0)) suggested that nitrogen availability could affect the color and lubricity of newly developed thalli. This study provides promising techniques for artificial cultivation of N. flagelliforme in the future.  相似文献   

13.
Nostoc flagelliforme Born. et Flah. is one of the terrestrial cyanobacteria naturally distributed in arid and semi-arid areas in the Northern and the North-western parts of China. The cyanobacterium is an edible delicacy with special medical value. However, commercial N. flagelliforme has nov been collected from the field only. For cultivation of this valuable cyanobacterium, it is necessary to understand how it grows and how it adapts to the environment.The experimental material was collected in Siziwangqi of Nei Monggol. The effects of light intensity, temperature, pH, salinity, length of thallus and rewetting on photosynthesis and respiration of N. fiagelli[orme were measured using an oxygen electrode. The results were as follows: The photosynthetic light compensation point was around 40–90μmol photons·m-2·s-1, the light saturation point was 1200μmol photons·m-2·s-1, and no photoinhibition appeared when the light intensity was increased to 1800μmol photons· m-2·s-1. N. fiagelliforme exhibited its photosynthetic and respiratory activities in the temperature range of 5–45℃. The optimum temperature for its photosynthesis was 25℃ and that for respiration was 35--40℃. Between pH range of 4.5–9.5 N. flagelliforme had photosynthetic activity and respiratory activity at pH range of 4-10, with optimum pH for photosynthesis at 7.5 and for respiration at 7.5–8.0. N. flagelliforme exhibited maximum net photosynthesis in 0.15mol/L of NaC1 in BG-11 medium. When the salinity was increased to 0.9 mol/L the net photosynthesis dropped down to zero. Respiration decreased concordantly with the increasing salinity as well. Maxima photosynthesis and respiration was also detected when the thallus of N. flagelliforme reached a length of 0.5cm and aftewords the more the length the less the activities. The recovery time attaining to the maximum photosynthesis and respiration activities after rewetting was dependent on storage time in dryness. The cyanobacterial mats after being reserved for 3 months, attained its maximum photosynthesis by 0.5h after rewetting, and that being reserved for 18 months needed 3.5h after rewetting. For respiration, the mats reserved for 3 months and 18 months required 5 minutes and lh after rewetting, respectively to attain its maximum. Under scanning electron microscope, cells of N. flagelliforme were wrapped up within a gluey sheath, and usually attached closely to each other in pairs and the filaments were uni-trichome with branches in some cases. The surface of thallus tip was rougher than other parts which meant that the tip portion had greater surface area beneficial to water absorption and cell growth.  相似文献   

14.
The terrestrial cyanobacterium Nostoc flagelliforme , inhabiting arid areas, withstands prolonged periods of dehydration. How dehydration and occasional wetting affect inorganic C acquisition in this organism is not well known. As inorganic C acquisition in cyanobacteria often involves carbonic anhydrases (CA), we studied the effect of cycles of hydration and dehydration on the extracellular and intracellular CA activities, at the pH values presumably associated with dew or rain wetting. The external CA of N. flagelliforme (or of the microorganismal consortium of which N. flagelliforme is the main component) is activated by hydration, especially at low pH, and it may facilitate inorganic C acquisition when N. flagelliforme colonies are wetted by dew. Internal CA is present in dry colonies and is rapidly inactivated upon rehydration, therefore an anaplerotic role for this enzyme is proposed.  相似文献   

15.
发菜的生态条件及其规律分析   总被引:5,自引:0,他引:5       下载免费PDF全文
 本文研究了甘肃永登和内蒙阿拉善左旗的发菜生态条件,发现了发菜生长中的水分节律现象。 发菜生于干燥的高原荒漠草原地带,属大陆性气候。其年平均气温为4.5—8℃,≥10℃积温为2231—2800℃·年,年温差大,昼夜温差明显。年平均降水量为201—290mm,集中在6—8月。年平均相对湿度为46—58%,有露水的天气约80天。土壤主要是由第三纪红土母质发育而来的棕钙土,营养贫乏,石灰质沉积明显,呈强碱性反应。年日照时数3000±300小时,辐射强烈。发菜在结构和生理上表现出强烈的旱生生态适应性,包括它的耐旱,耐贫瘠,嗜阳、嗜碱以及对温度变化的适应性强。 发菜生长中具有明显的水分节律现象。在5—10月,在暂短的降雨和露水后,藻体迅速吸取水分而得以生长。尔后,水分又很快被蒸发,藻体变干,生长停滞。发菜在这种湿润⇌干燥的反复节律中得到不断的断续生长和积累,从而完成发菜在干燥条件下的年生长过程。  相似文献   

16.
高压冷冻和低温替代技术制备的发菜营养细胞的超微结构   总被引:2,自引:0,他引:2  
祝建  王俊 《Acta Botanica Sinica》1998,40(10):901-905
应用高压冷冻和低温替代技术系统研究了发菜(NostocflageliformeBorn.etFlah.)营养细胞的超微结构并与常规方法进行了比较。结果显示:在化学固定、脱水和包埋后,细胞结构出现一些人为的改变。而应用高压冷冻和低温替代技术,细胞和胶质鞘之间不会出现大的间隙并且细胞质也很少收缩。细胞内各种膜结构清晰可见。有关大量细菌位于发菜的胶质鞘中以及细胞中具有大的液泡是首次报道。  相似文献   

17.
对野生发菜(Nostocflagelliforme Bom.et Flab)的膜脂(主要成分为类囊体膜脂)及其脂肪酸组成进行了测定分析.发菜的膜脂由单半乳糖甘油二酯(MGDG)、双半乳糖甘油二酯(DGDG)、磷酯酰甘油(PG)和硫代异鼠李糖甘油二酯(SQDG)组成,其酯酰基连接有棕榈酸(16:0)、十六碳烯酸(16:1)、硬脂酸(18:0)、油酸(18:1)、亚油酸(18:2)和亚麻酸(18:3)6种脂肪酸.发菜的不饱和脂肪酸含量可达总脂的73%,特别是16:1和18:3分别高达29%和34%,远远高于已报道的其他蓝藻,说明了发菜类囊体膜具有较强的抗逆性特点.同时还对复水30 min和复水后生长24 h的发菜膜脂及其脂肪酸组成进行了分析.结果表明,复水对野生发菜的膜脂及其脂肪酸组成没有显著影响,说明发菜的膜脂和脂肪酸组成在干燥-吸水过程中能保持很高的稳定性.  相似文献   

18.
Nostoc flagelliforme Born. et Flah is highly adapted to drought stress, cold and light stresses, and suitable for growing in the unfavorable areas. This paper presents the results of the analysis of the membrane (mainly thylakoid membrane) lipids from N. flagelliforme in order to investigate the relationship between membrane lipid composition and stress resistance to this cyanobacteria. The membrane lipids are composed of monogalactosyl diacylglycerol (MGDG), digalactosyl diacylglycerol (DGDG), sulfoquinovosyl diacylglycerol (SQDG) and phosphatidylglycerol (PG). The major fatty acids in these lipids are palmitic (16∶0), palmitoleic (16∶1), stearic (18∶0), oleic (18∶1), linoleic (18∶2) and linolenic (18∶3) acids. In N. flagelliforme, polyunsaturated fatty acids account for 73% of the total fatty acids, much higher than that of the other cyanobacteria reported so far. Among which 16∶1 and 18∶3 are as high as 28.9% and 34.3% respectively. The high resistance of N. flagelliforme to abnormal conditions may be associated with the extent of unsaturation of fatty acids. In addition, the wild N. flagelliforme treated with water for 30 min and cultured for 24 h and the lipid and fatty acid composition were found to be not affected by water-absorption.  相似文献   

19.
发菜(Nostoc flagelliforme)是一种陆生固氮蓝藻,具有强烈的旱生生态适应性.运用双向电泳技术、凝胶图像分析、MALDI-TOF-TOF/MS质谱鉴定和数据库检索,发现发菜Ferritin在干旱胁迫条件下表达量逐渐降低.根据鉴定的Ferritin已知氨基酸序列设计简并性引物克隆该基因,获得了长度为540 bp的DNA,GenBank登陆号为HM854287.序列比较显示该基因具有较高的保守性,蛋白质二级结构主要由α螺旋和随机卷曲构成.RT-PCR分析表明,Ferritin mRNA在干旱胁迫条件下表达量逐渐降低,与Ferritin的表达趋势一致.将Ferritin基因在大肠杆菌中表达,获得符合预期的外源重组蛋白(22.4 kD).实验结果可为进一步研究发菜耐旱的分子机理及探讨发菜对极端干旱环境的适应和保护机制奠定基础.  相似文献   

20.
glmM编码的磷酸葡糖胺变位酶是肽聚糖合成前体的关键酶。为探究发菜glmM响应干旱胁迫的表达调控机制及明确其分子信息,本研究对干旱胁迫条件下发菜glmM在转录水平的差异表达进行了分析,并对glmM的表达水平、磷酸化修饰、乙酰化修饰和琥珀酰化修饰水平进行了检测,克隆了发菜glmM,进行了序列分析和原核表达。结果表明,干旱胁迫条件下,发菜glmM在转录水平上的表达量先增加后减少,glmM上调表达,glmM的磷酸化修饰水平逐渐增加,乙酰化修饰水平相对稳定,琥珀酰化修饰水平有明显变化。设计特异性引物克隆glmM基因,获得全长1416 bp发菜glmM基因,与肺衣(5183)glmM的核苷酸序列同源性为95%,氨基酸同源性为97%。将glmM在大肠杆菌中表达,获得一个51.45 kD的外源蛋白,MALDI-TOF-TOF/MS分析证明该蛋白为磷酸葡糖胺变位酶。研究结果为深入研究发菜glmM的分子信息、生物学功能及其响应干旱胁迫的分子机制提供帮助。  相似文献   

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