CO_2浓度变化对两种淡水绿藻的显微结构和超微结构的影响(英)

为了探讨淡水绿藻在适应CO2 浓度变化过程中细胞形态和结构的变化 ,通过普通显微镜和电子显微镜观察了在不同CO2 浓度培养下的莱因衣藻 (ChlamydomonasreinhardtiiDang)和斜生栅藻 (ScenedesmusobliquusK櫣ｔｚ)细胞。结果表明 ,CO2 浓度变化对莱因衣藻细胞体积没有明显的影响 ,但斜生栅藻在低浓度CO2 培养下细胞体积明显增大 ,并可见细胞内含有大量颗粒。两种绿藻细胞的超微结构显示 ,在低浓度CO2 培养下 ,细胞内叶绿体数目明显减少 ,并可见明显的淀粉盘包围的蛋白核 ;细胞内还可见大量的淀粉粒。而在高浓度CO2 培养下 ,这两种绿藻细胞内均未见明显的蛋白核和大量淀粉粒出现。     

CO2浓度变化对两种淡水绿藻的显微结构和超微结构的影响

为了探讨淡水绿藻在适应CO2党旗变化过程中细胞形态和结构的变化,通过普通显微镜和电子显微镜观察了在不同CO2浓度培养下的莱因衣藻（Chlamydomonas reinhardtii Dang）和斜生栅藻（Scenedesmus obliquus Kuetz）细胞。结果表明,CO2浓度变化对莱因衣藻细胞体积没有明显的影响,但斜生栅藻在低浓度CO2培养下细胞体积明显增大,并可见细胞内含有大量颗粒,两种绿藻细胞的超微结构显示,在低浓度CO2培养下,细胞内叶绿体数目明显减少,并可见明显的淀粉盘包围的蛋白核;细胞内还可见大量的淀粉粒。而在高浓度CO2培养下,这两种绿藻细胞内均未见明显的蛋白核和大量淀粉粒出现。     

极高CO2胁迫对被甲栅藻(Scenedesmus armatus)生理活性和细胞结构影响

以被甲栅藻(Scenedesmus armatus)为材料研究极高浓度CO2对其生理活性和细胞结构的影响.研究表明,被甲栅藻能在60%的CO2浓度下快速生长,在5%、20%、40%、60%、80%、100% CO2浓度下的平均增长率分别是1.228、0.925、0.741、0.305、0.042、0.001 g·L-1·d-1 DW.通入极高浓度CO2(20%、40%)后,被甲栅藻细胞的光系统II(PSII)最大光化学效率(Fv/Fm)在24 h内明显下降,对PSII抑制作用较明显;其后,随培养时间的增长而逐渐恢复正常.显微结构和亚显微结构显示极高CO2浓度下培养了6 d的藻细胞体积稍膨大、颗粒化,色素体结构相对不完整,类囊体膜结构略显松散,蛋白核消失,细胞内的液泡数目增多.     

6种微藻对氯霉素和硫酸新霉素敏感性研究

目的:探讨3种真眼点藻(点状魏氏藻(Visderia punctata)、波氏真眼点藻(Eustigmatos polyphem)、魏氏真眼点藻(Eustigmatos vischeri))和3种绿藻(栅藻(Scnedesmus sp.)、斜生栅藻(Scenedesmus obliqulis)、爪哇栅藻(Scenedesmus jaoaensis))对2种抗生素的敏感性.方法:采用藻液细胞计数法和藻细胞固体平板培养法研究了氯霉素和硫酸新霉素对6种微藻生长的影响.结果:液体培养,3种绿藻对氯霉素敏感性均高于硫酸新霉素,10μg·mL-1氯霉素即可明显抑制3种绿藻的生长(P＜0.05),而硫酸新霉素在浓度为200 μg·mL-1时才显示出明显抑制作用:3种真眼点藻对2种抗生素都不敏感.固体培养,除波氏真眼点藻外,其它5种微藻对氯霉素的致死浓度均为50μg·mL-1;波氏真眼点藻、栅藻、斜生栅藻和爪哇栅藻对硫酸新霉素的致死浓度分别为100 μg·mL-1、200μg· mL-1、50μg·mL-1和50μg·mL-1.结论:氯霉素可作为选育6种微藻抗性突变株的筛选剂.     

梭鱼草化感物质丁二酸对微囊藻和栅藻生长及竞争的影响

为了解梭鱼草(Pontederia cordata)根茎有机酸类化感物质对铜绿微囊藻(Micro-cystis aeruginosa,M)和斜生栅藻(Scenedesmus obliquus,S)生长和竞争关系的影响,将不同浓度丁二酸作用于两种藻的单种培养和共培养,即铜绿微囊藻与斜生栅藻初始比例为1∶0(100%M)、1∶1(50%M+50%S)、2∶3(40%M+60%S)、3∶2(60%M+40%S)、0∶1(100%S)。结果表明:丁二酸对铜绿微囊藻和斜生栅藻均有抑制作用,抑制能力与浓度呈正相关;无化感物质作用下,单种培养和共培养中铜绿微囊藻生长能力均强于斜生栅藻; 60mg·L-1丁二酸处理下,40%M+60%S、50%M+50%S培养组中β(斜生栅藻对铜绿微囊藻的抑制参数)0,60%M+40%S培养组中β0,表明藻类初始比例影响蓝绿藻之间竞争;丁二酸可改变蓝绿藻之间竞争关系,低浓度(20、40 mg·L-1)作用下,表现为铜绿微囊藻抑制斜生栅藻,斜生栅藻促进铜绿微囊藻,高浓度(60、80 mg·L-1)作用下,表现为两者相互抑制,表明两种藻之间竞争加强。     

斜生栅藻对振荡和磷胁迫的生理生化响应

为了探讨水文条件的变化对常见绿藻水华发生的潜在影响,实验以斜生栅藻为材料,研究了不同水流状态及磷浓度对其生长及磷利用策略的影响。实验分别设置静止条件(0 r/min)、低振荡条件(90 r/min)和高振荡条件(120 r/min),同时设置磷限制(0.2 mg/L)和磷充足(2 mg/L)两组磷浓度,整个实验过程为3周。实验过程测定的指标为:比生长速率、胞外碱性磷酸酶活性、叶绿素a含量以及磷吸收动力学参数。实验结果表明:(1)同静止条件相比,低振荡和高振荡条件均能显著降低斜生栅藻的比生长速率,但是两种不同磷浓度下其比生长速率却无显著性差异。(2)在实验第21天时,振荡条件培养下,斜生栅藻的胞外碱性磷酸酶活性显著高于静止条件培养,与此相反,胞内磷浓度却显著高于静止条件。(3)在磷限制条件下斜生栅藻的叶绿素a含量显著降低,同时两种振荡条件培养均使其在磷充足条件下叶绿素a含量降低。(4)通过磷吸收动力学参数的比较,静止条件培养的斜生栅藻对磷的亲和力高于其在振荡条件下。由此可见,斜生栅藻适应于静止无扰动且磷营养丰富的水体,随着水体中磷浓度进一步升高,静止和水流缓慢的水体存在导致像斜生栅藻这一类绿藻发生水华的风险。       

重金属铅与两种淡水藻的相互作用

为了研究重金属铅与淡水藻类之间的相互作用,采用不同Pb2+浓度处理铜绿微囊藻(Microcysis aeruginosa Kutz.)和斜生栅藻[Scenedesmus obliquus(Turp.)Kutz.],分别对两种藻的生物量、藻液电导率、O-·2含量、过氧化物酶(POD)、过氧化氢酶(CAT)活性以及藻对Pb2+的吸收作用等进行了测定,并通过扫描电镜观察了不同Pb2+浓度处理下两种藻细胞的表面结构。结果显示:(1)Pb2+浓度低于3 mg/L促进铜绿微囊藻生长,高于9 mg/L抑制其生长;但在3—12 mg/L范围内,Pb2+均明显抑制了斜生栅藻的生长,说明斜生栅藻对Pb2+毒性的敏感程度要高于铜绿微囊藻。(2)受到铅离子的胁迫,两种藻细胞膜通透性均有一定改变,扫描电子显微镜的照片观察,两种藻细胞表面的絮状物随着Pb2+的升高而增多,尤其是斜生栅藻细胞结构改变明显,多数细胞变形破裂;同时,O-·2含量升高,POD、CAT活性早期均可随Pb2+的增加而上升,表明氧自由基的产生增多以及由其引起的细胞生理生化改变可能是铅离子作用于藻细胞的主要机制。(3)两种淡水藻对Pb2+均有吸收作用,单位量藻细胞内,斜生栅藻对Pb2+的吸收能力好于铜绿微囊藻。所有结果提示:斜生栅藻不仅可以作为对重金属敏感的指示生物来监测水体Pb2+污染程度;同时由于斜生栅藻比铜绿微囊藻具有更好的Pb2+吸收能力,因此还可以利用斜生栅藻作为处理水体Pb2+的生物材料。     

斜生栅藻对不同形态锑胁迫的响应及抗性研究

该研究以斜生栅藻(Scenedesmus obliquus)为研究对象,研究不同浓度的Sb(Ⅲ)、Sb(Ⅴ)胁迫下对斜生栅藻生长速率、叶绿素a、抗氧化酶活性和细胞表面结构的影响,以探讨重金属胁迫下斜生栅藻的抗性机理。结果表明:(1)在高浓度Sb(Ⅲ)、Sb(Ⅴ)胁迫处理中,斜生栅藻生长对Sb(Ⅲ)胁迫的响应更加迅速;随着Sb(Ⅲ)、Sb(Ⅴ)胁迫浓度增加,斜生栅藻体内叶绿素a含量呈下降趋势,且对Sb(Ⅲ)胁迫浓度的变化反应更为敏感。(2)在800μmol/L Sb(Ⅲ)和Sb(Ⅴ)胁迫下,斜生栅藻体内丙二醛(MDA)含量及超氧化物歧化酶(SOD)活性分别在胁迫第7~8天和第6~7天时变化更为明显;过氧化氢酶(CAT)活性在胁迫处理的第4~5天就迅速增加,对Sb胁迫响应比SOD更为迅速。(3)在高浓度Sb(Ⅲ)、Sb(Ⅴ)胁迫下,斜生栅藻细胞结构受到严重损伤,而且Sb(Ⅲ)对斜生栅藻细胞的损伤更加明显。研究发现,Sb(Ⅲ)、Sb(Ⅴ)对斜生栅藻生长、叶绿素a及细胞结构表现出不同程度的抑制和破坏作用,其细胞受到的影响程度与Sb(Ⅲ)、Sb(Ⅴ)的处理浓度及处理时间均密切相关,但斜生栅藻依靠自身抗氧化酶系统在一定程度上能够缓解Sb胁迫的不利影响。     

水芹水浸提液对斜生栅藻的化感效应研究

采用栅藻在不同浓度的水芹水浸提液中纯培养的方法,研究了水芹水浸提液对斜生栅藻细胞数、叶绿素含量及藻细胞超微结构的影响。结果显示,10 g·L^-1水芹水浸提液对斜生栅藻的生长和叶绿素含量的增加具有明显的促进效应;20 g·L^-1水芹水浸提液对藻细胞数和叶绿素含量的增加持续到第3 d,3 d后出现显著的抑制效应;高浓度（30~50 g·L^-1）水芹水浸提液对藻细胞数和叶绿素含量的明显抑制在第2 d始现,随时间延长而加剧,并具有浓度效应;40 g·L^-1水芹水浸提液处理后,斜生栅藻细胞壁断裂甚至消失,细胞中叶绿体片层肿胀甚至解体,核膜破裂,核质外渗。水芹水浸提液对斜生栅藻具有化感效应,低浓度促进生长,高浓度抑制。     

栅列藻细胞核的铁矾醋酸-洋红染色

栅列藻(Scenedesmus sp.)是一种很重要的单细胞或群体绿藻,因其生长繁殖快,生活周期短,易于培养,故在近代藻类培养和生理生化研究中为各国学者所广泛应用. 栅列藻的细胞个体极小,长度一般小于10微米.在自然水体中常以2或4或8或16个细胞排列成定形群体而存在.人工培养时,细胞分散成单个.栅列藻的细胞壁厚且致密加之细胞内含量丰富的叶绿素,对细胞核有很大的遮掩性,因此,栅列藻细胞核的染色一直存在着     

高浓度CO2培养条件下极大螺旋藻光抑制研究

以极大螺旋藻作为实验材料,研究了不同CO2浓度培养对螺旋藻光抑制和恢复的影响,结果表明由光抑制导致的光合速率下降,高浓度CO2比低浓度CO2培养程度小,在高浓度CO2条件下培养的极大螺旋藻,虽然在强光下也表现出光抑制,但与低浓度CO2相比,光合速率下降得较慢。这种现象在强光与弱光培养均存在,但强光培养时更明显。光抑制后的恢复实验表明,不同CO2浓度培养的极大螺旋藻,光系统光化学活性(Fv/Fm)在弱光下恢复较好,高光强、高浓度CO2培养的藻,恢复速度稍快;而在黑暗中,几乎没有恢复;在弱光和含氯霉素的条件下Fv/Fm均下降。由此可见,高CO2浓度可减轻极大螺旋藻的光抑制,但对其光抑制后的恢复影响不大。       

Impacts of Elevated CO2 Concentration on Biochemical Composition,Carbonic Anhydrase, and Nitrate Reductase Activity of Freshwater Green Algae

To investigate the biochemical response of freshwater green algae to elevated CO2 concentrations,Chlorella pyrenoidosa Chick and Chlamydomonas reinhardtii Dang cells were cultured at different CO2concentrations within the range 3-186 μmol/L and the biochemical composition, carbonic anhydrase (CA),and nitrate reductase activities of the cells were investigated. Chlorophylls (Chl), carotenoids, carbonhydrate,and protein contents were enhanced to varying extents with increasing CO2 concentration from 3-186μmol/L. The CO2 enrichment significantly increased the Chl a/Chl b ratio in Chlorella pyrenoidosa, but not in Chlamydomonas reinhardtii. The CO2 concentration had significant effects on CA and nitrate reductase activity. Elevating CO2 concentration to 186 μmol/L caused a decline in intracellular and extracellullar CA activity. Nitrate reductase activity, under either light or dark conditions, in C. reinhardtii and C. pyrenoidosa was also significantly decreased with CO2 enrichment. From this study, it can be concluded that CO2enrichment can affect biochemical composition, CA, and nitrate reductase activity, and that the biochemical response was species dependent.     

高浓度CO_2培养条件下极大螺旋藻光抑制研究

以极大螺旋藻作为实验材料 ,研究了不同 CO2 浓度培养对螺旋藻光抑制和恢复的影响 ,结果表明由光抑制导致的光合速率下降 ,高浓度 CO2 比低浓度 CO2 培养程度小 ,在高浓度 CO2 条件下培养的极大螺旋藻 ,虽然在强光下也表现出光抑制 ,但与低浓度 CO2 相比 ,光合速率下降得较慢。这种现象在强光与弱光培养均存在 ,但强光培养时更明显。光抑制后的恢复实验表明 ,不同 CO2 浓度培养的极大螺旋藻 ,光系统 光化学活性 (Fv/Fm)在弱光下恢复较好 ,高光强、高浓度 CO2 培养的藻 ,恢复速度稍快 ;而在黑暗中 ,几乎没有恢复 ;在弱光和含氯霉素的条件下 Fv/Fm均下降。由此可见 ,高 CO2 浓度可减轻极大螺旋藻的光抑制 ,但对其光抑制后的恢复影响不大。     

CO2 limitation induces specific redox-dependent protein phosphorylation in Chlamydomonas reinhardtii

Acclimation of the green alga Chlamydomonas reinhardtii to limiting environmental CO2 induced specific protein phosphorylation at the surface of photosynthetic thylakoid membranes. Four phosphopeptides were identified and sequenced by nanospray quadrupole TOF MS from the cells acclimating to limiting CO2. One phosphopeptide originated from a protein that has not been annotated. We found that this unknown expressed protein (UEP) was encoded in the genome of C. reinhardtii. Three other phosphorylated peptides belonged to Lci5 protein encoded by the low-CO2-inducible gene 5 (lci5). The phosphorylation sites were mapped in the tandem repeats of Lci5 ensuring phosphorylation of four serine and three threonine residues in the protein. Immunoblotting with Lci5-specific antibodies revealed that Lci5 was localized in chloroplast and confined to the stromal side of the thylakoid membranes. Phosphorylation of Lci5 and UEP occurred strictly at limiting CO2; it required reduction of electron carriers in the thylakoid membrane, but was not induced by light. Both proteins were phosphorylated in the low-CO2-exposed algal mutant deficient in the light-activated protein kinase Stt7. Phosphorylation of previously unknown basic proteins UEP and Lci5 by specific redox-dependent protein kinase(s) in the photosynthetic membranes reveals the early response of green algae to limitation in the environmental inorganic carbon.     

CO metabolism of Desulfovibrio vulgaris strain Madison: physiological function in the absence or presence of exogeneous substrates

Abstract Trace amounts of carbon monoxide were produced and subsequently consumed during the growth of Desulfovibrio vulgaris on organic electron donors. D. vulgaris also utilized carbon monoxide as the sole electron donor for growth and sulfate reduction. Growth of D. vulgaris on CO, H₂ or organic electron donors was inhibited at ≥4.5% CO in the culture headspace. At lower CO concentrations, hydrogen was produced as a consequence of CO consumption and consumed when the CO partial pressure was decreased. The rate of CO consumption was ten-fold higher in D. vulgaris grown on either CO, lactate or pyruvate than when cells were grown on H₂ as electron donor. The physiological function of CO metabolism and a CO-dependent hydrogen cycle in D. vulgaris is discussed.     

CO_2加富对UV-B辐射胁迫下亚心形扁藻光合作用和膜脂过氧化以及抗氧化酶活性的影响(英文)

在CO2浓度分别为当今CO2浓度(360 mL/L)和加富浓度(5 000 mL/L)条件下,研究了UV-B胁迫对亚心形扁藻(Platymonas subcordiformis (Wille) Hazen)的光合作用、膜脂过氧化和抗氧化酶活性的影响。实验结果表明:(1) UV-B单独作用下,亚心形扁藻的干重、光合速率、叶绿素a (Chl a)和类胡萝卜素(Car.)含量显著降低,CO2加富单独作用下,亚心形扁藻的干重和光合速率显著升高,叶绿素a和类胡萝卜素含量与对照相比没有显著变化,而UV-B与CO2共同作用则使亚心形扁藻的干重和光合速率与对照相比没有显著变化,叶绿素a和类胡萝卜素含量显著降低。(2) UV-B单独作用和CO2加富单独作用都使可溶性蛋白含量显著降低,UV-B与CO2共同作用下的可溶性蛋白含量比UV-B单独作用的要高。高CO2对藻的可溶性蛋白含量的变化在很大程度上归因于Rubisco蛋白的降低。(3)UV-B单独作用下,O2-. 产生速率、H2O2 含量和MDA含量显著升高,而CO2加富单独作用下,O2-. 产生速率、H2O2 含量和MDA含量显著降低,与UV-B单独作用相比,UV-B与CO2共同作用使O2-. 产生速率、H2O2 含量和MDA含量显著降低。说明CO2加富可以减少活性氧对亚心形扁藻的氧化胁迫,同时减少UV-B对亚心形扁藻的膜脂过氧化伤害。(4) UV-B单独作用下,SOD、POD、CAT、GR和GPX活性显著升高,高CO2     

Degradation by Streptomyces viridosporus T7A of plant material grown under elevated CO2 conditions

The biodegradability of plant material derived from wheat grown under different concentrations of atmospheric CO2 was investigated using the lignocarbohydrate solubilising actinomycete, Streptomyces viridosporus. Growth of S. viridosporus and solubilisation of lignocarbohydrate were highest when wheat grown at ambient CO2 concentrations (350 ppm) was used as C-source. Growth of S. viridosporus and solubilisation were reduced when the plant material was derived from wheat grown at 645 ppm CO2. The results suggest that modifications in plant structure occur when wheat is grown under conditions of elevated atmospheric CO2 which make it more resistant to microbial digestion.     

Identification and regulation of high light-induced genes in Chlamydomonas reinhardtii

We have used restriction fragment differential display for isolating genes of the unicellular green alga Chlamydomonas reinhardtii that exhibit elevated expression on exposure of cells to high light. Some of the high light-activated genes were also controlled by CO2 concentration. Genes requiring both elevated light and low CO2 levels for activation encoded both novel polypeptides and those that function in concentrating inorganic carbon (extracellular carbonic anhydrase, low CO2-induced protein, ABC transporter of the MRP subfamily). All the genes in this category were shown to be under the control of Cia5, a protein that regulates the responses of C. reinhardtii to low-CO2 conditions. Genes specifically activated by high light, even under high-CO2 conditions, encoded a 30 kDa chloroplast membrane protein, a serine hydroxymethyltransferase, a nuclease, and two proteins of unknown function. Experiments using DCMU, an inhibitor of photosynthetic electron transport, and mutants devoid of either photosystem I or photosystem II activity, showed aberrant expression of all the genes regulated by both CO2 and high light, suggesting that redox plays a role in controlling their expression. In contrast, there was little effect of DCMU or lesions that block photosynthetic electron transport on the activity of genes that were specifically controlled by high light.     

Increasing carbon dioxide from five percent to ten percent improves rabbit blastocyst development from cultured zygotes.

One-cell rabbit zygotes were cultured at 39 degrees C in basal synthetic medium II (BSM-II) with 5%, 10%, or 15% CO2 and humidified air to determine the effect of CO2 concentration on development in vitro. After 4 days in culture, 37% of the embryos grown in 10% or 15% CO2 had reached the hatching blastocyst stage, but only 10% of the embryos were hatching when cultured under 5% CO2 (P = 0.01). Over all blastocysts, cell numbers were 207, 246, and 205 for the 5%, 10%, and 15% CO2 treatments, respectively. In a second experiment to determine if there was a beneficial effect, particularly at the blastocyst stage, of a higher concentration of CO2, embryos were cultured 4 days in either 5% or 10% CO2 or for 2 days in 5% CO2 followed by 2 days in 10% CO2. The numbers of blastomeres per embryo and embryo diameter were greater (P < 0.05) in embryos cultured continuously in 10% CO2 or in 10% CO2 only during days 3 and 4 of culture than in embryos cultured continuously in 5% CO2. In a third experiment, one-cell rabbit zygotes were cultured with 5% or 10% CO2 in a defined, protein-free medium consisting of 1:1 RPMI 1640 and Dulbecco's modified Eagle's medium. The proportion of embryos hatching and cell counts were significantly greater (P < 0.01) when cultured in the presence of 10% CO2. These data indicate that a 10% CO2 atmosphere exerts a beneficial effect on the development of zygotes into expanding and hatching rabbit blastocysts in vitro.