有被膜的

基本解释 (translations)

tunicate  ·  incapsuled

与有被膜的相关的网络例句 [注：此内容来源于网络，仅供参考]

The patterns of amyloplast proliferation behaved "amyloplast envelop dilating, evaginating, and budding to form new amyloplast","amyloplast envelop constricting to form new amyloplast","form new amyloplast as the middle clapboard" and "amyloplast envelope dilating and invaginating to form new amyloplast".

玉米胚乳细胞淀粉质体增殖有"被膜出泡、外凸，以出芽方式形成淀粉质体"、"淀粉质体被膜缢缩形成淀粉质体"、"以中间隔板形式形成淀粉质体"及"淀粉质体被膜向内出泡，在淀粉质体内形成新的淀粉质体"等几种方式。

The patterns of amyloplast proliferation behaved "amyloplast envelop dilating, evaginating, and budding to form new amyloplast","amyloplast envelop constricting to form new amyloplast","form new amyloplast as the middle clapboard" and "amyloplast envelope dilating and invigilating to form new amyloplast".

玉米胚乳细胞淀粉质体增殖有被膜出泡、外凸，以出芽方式形成淀粉质体；淀粉质体被膜缢缩形成淀粉质体；以中间隔板形式形成淀粉质体；淀粉质体被膜向内出泡，在淀粉质体内形成新的淀粉质体等几种方式。

The double membrane vesicle, which was produced by budding of the outer membrane of amyloplast, accumulated starch to form new amyloplast. The double membranes of amyloplast invaginated and the inner membrane dilated to form new amyloplast in the amyloplast.

淀粉质体增殖产生新淀粉质体有多种方式：出芽增殖、缢缩增殖、中间隔板增殖、被膜向内出泡或内陷增殖、被膜形成双层膜小泡再积累淀粉增殖，它们均是淀粉质体被膜的一种膜行为。

Under normal temperature.the Ca2+-ATPase activity was found on the innerside of the PM.on the vacuole envelope and the chloroplast envelope,and theenzyme activity declined upon heat stress.The Ca2+-ATPase activity on the vacuoleenvelope,PM.and the chloroplast envelope in both Ca2+-and oxalate-treated peppermesophyll cells was higher than that in the control under the same condition.TheCa2+-ATPase was also found at the granum lamella,and it was activatedsignificantly by exogenous Ca2+ and oxalate treatments.Under heat stress.the Ca2+-ATPase activity declined slowly in both Ca2+- and oxalate-treated mesophyll cells.But La3+ treatment inhibited the enzyme activity under both normal condition andheat stress.

常温下生长的叶肉细胞，在质膜、液泡膜、叶绿体被膜等处有Ca2+-ATPase活性，热胁迫后酶活性下降；外源Ca2+和草酸预处理对辣椒叶肉细胞各种膜上Ca2+-ATPase活性具有促进作用，特别是定位于液泡膜、质膜和叶绿体被膜上的酶活性明显比对照提高；在叶绿体基粒和基质片层上也有酶活性，并且Ca2+和草酸预处理对该部位上的酶活性激活作用更明显；La3+处理的作用与Ca2+和草酸处理的效果相反。

Protease treatment of the plasma membranes could abolish the binding but NaIO_4 and glycosidase could not, indicating that nsLTP144 bound to plasma membranes protein without carbohydrate moiety. Using the homobifunctional cross-linking regent bissuberate (BS~3) and rice plasma membranes incubated with ~(125)I-Trx-nsLTP144, we identified, after SDS-polyacrylamide gel electrophoresis and autoradiography, a putative protein receptor on the rice plasma membranes with the molecular mass around 60 kDa. NsLTP144 can not trigger extracelluar alkalization in arabidopsis, but can abolish the extracellular alkalization effect of phytopathogen elicitor cryptogein, suggesting that cryptogein and nsLTP144 may bind to the same membrane protein. In vitro pull-down assay showed that nsLTP144 interacted with OsCaM1, a possible extracellular calmodulin, implying that nsLTP144 and OsCaM1 could function in the same signal transduction pathway. These results shed light on revealing the roles of nsLTP in vivo and make it promising to finally characterize the plasma membranes receptor of nsLTP.

发现~(125)I-Trx-nsLTP144、~(125)I-Trx-nsLTP110与水稻细胞质膜均具有特异性结合，而且结合是饱和性的、可被竞争的，符合配体-受体结合的典型特征，同时用于对照实验的蛋白质~(125)I-Thioredoxin没有此特性，表明水稻细胞质膜上存在nsLTP的受体；利用可氧化糖基的NaIO_4和水解糖基的N\'-糖苷酶F处理水稻细胞质膜，再进行结合实验，结合活性几乎不受影响；而利用胰蛋白酶处理细胞膜则使得结合能力几乎完全丧失，表明其受体为没有经过糖基化修饰的蛋白质；利用交联剂BS~3交联配体一受体后，再进行SDS-PAGE分离和放射自显影，结果显示水稻细胞质膜上的nsLTP受体中有一个60kDa的蛋白质可以与nsLTP144发生特异性的结合，可能是其受体；细胞外碱化实验表明，nsLTP144不能促使拟南芥原生质体细胞培养液的细胞外碱化反应，却能猝灭来自植物病原菌的激发子Cryptogein刺激拟南芥原生质体产生的细胞外碱化反应，表明nsLTP和Cryptogein结合细胞膜上相同的位点，保护了植物细胞免受Cryptogein导致的细胞程序性死亡，并诱导系统获得性抗性的产生；体外Pull-down实验表明，nsLTP144和水稻的OsCaM1具有相互作用，暗示了nsLTP144和OsCaM1可能同在一个信号通路上起作用。

Grew on the normal temperature, it was shown that the deposits of calcium antimonate being the indicator for Ca(superscript 2+) localization mainly concentrated within the vacuoles and intercellular spaces and there was also some Ca(superscript 2+) deposits in cell walls. But when Garyota urens L. was treated by the temperature of 2℃ for 48 h, the level of Ca(superscript 2+) increased in cytoplasm and plasma membrane, but decreased in vacuoles and intercellular spaces considerably. At the same time, the ultrastructure of chloroplasts suffered from chilling: the membrane of chloroplasts had been damaged, the layer of thylakoids was exiguous and unclear, the photosynthetic rate decreased evidently. And when Garyota urens L. was treated by the temperature of 2℃ for 120 h, the deposits of Ca(superscript 2+) mainly concentrated within the cytoplasm, nucleus and plasma membrane and there was also some Ca(superscript 2+) deposits in vacuoles, and the ultrastructure of some cells was simultaneously damaged severely: Chloroplasts structure, vacuole membrane and nuclear membrane had been damaged fully, the structure within the cell had become unclear, and the cell only have respiration.

研究结果表明，未经低温处理的董棕幼苗叶肉细胞，焦锑酸钙沉淀颗粒大量出现在液泡和细胞间隙中，细胞壁中也可见少量沉淀，而细胞基质中则看不到焦锑酸钙沉淀；经2℃ 48 h低温处理后，细胞基质和细胞膜上焦锑酸钙沉淀增加，而液泡和细胞间隙中的焦锑酸钙沉淀则显著减少，并且超微结构已初步显示出寒害的特徵，叶绿体外膜部分破损，类囊体片层稀疏且排列不规则，光合速率明显下降等；经2℃ 120 h低温处理后，细胞间隙内的焦锑酸钙沉淀极少，有的也紧贴在细胞外壁上，而细胞基质和细胞膜上则分布有非常多的焦锑酸钙沉淀，在核基质和液泡中也可见到少量的焦锑酸钙沉淀，并且超微结构遭到了显著破坏，叶绿体结构完全被破坏，核膜与液泡膜严重破损，内部结构模糊，细胞只表现为呼吸作用，不进行光合作用。

The micelle granules were accumulated in the guttate structure. Both liquid crystal phase and isotropic phase coexisted here. With the volatilization of solvent, the structures can change from disc or hexagon to cube with the variation of environment and interior reciprocity.

结果表明，在该薄膜中有被冻结的液晶滴状结构，随着溶剂的挥发，膜体系内氢键的种类和数目发生改变，壳聚糖胶束颗粒聚集成圆盘或六角状，体现为同心环堆积，一定时间后转变为立方环状结构。

The sex pheromone-producing gland of Ancylis.sativa Liu is amodified intersegmental membrane as a dorsal bag between eighth and ninthabdominal segments.

对枣粘虫雌蛾性信息素腺体的扫描和透射电镜观察表明，枣粘虫性信息素腺体是由第八、九腹节间的节间膜特化而成，是位于背部的一个囊状结构，它由两部分构成，前部的方形囊状体和后部的三角形囊状体，二者之间有一突起的脊；雌蛾静止时，腺体随第八和第九腹节一起嵌缩于第七腹节内，求偶时，腹部末端外伸，腺体细胞表皮外露，释放性信息素；腺体细胞呈方形，其表面覆盖几丁质表皮，表皮顶端无孔；细胞核很大，呈椭圆形，由双层核膜包被，位于细胞中下部，内有丰富的染色质；细胞质内有丰富的内质网，其内还有大量的大小不等的脂肪滴，以及线粒体和溶酶体等细胞器。

The patterns of amyloplast proliferation behaved "amyloplast envelop dilating, evaginating, and budding to form new amyloplast","amyloplast envelop constricting to form new amyloplast","form new amyloplast as the middle clapboard" and "amyloplast envelope dilating and invaginating to form new amyloplast".

玉米胚乳细胞淀粉质体增殖有&被膜出泡、外凸，以出芽方式形成淀粉质体&、&淀粉质体被膜缢缩形成淀粉质体&、&以中间隔板形式形成淀粉质体&及&淀粉质体被膜向内出泡，在淀粉质体内形成新的淀粉质体&等几种方式。

We hypothesize that a transition from lysines to arginines such as that observed in tunicates (30), in conjunction with a loss of the core region, could have resulted in the differentiation of the arginine-rich protamines of the P type.

我们假定从离氨酸到 arginines 的一个转变如此的当做观察在有被膜的(30)，连同核心区域的一个损失，可能造成 arginine 的区别-p 类型的富有 protamines。

与有被膜的相关的网络解释 [注：此内容来源于网络，仅供参考]

basement membrane：基底膜

如透明角质颗粒、被膜颗粒、张力原纤维等. 这些成分中任何一种如有缺乏,均可影响角质的形成. 由于角质上层细胞间的桥粒逐渐消失,使它们能有规律的脱落,保持表皮的正常厚度. (六)基底膜 基底膜(Basement membrane)是真皮和表皮的交界,在

decapod：十足类/有十脚的

decapitator /断头器/ | decapod /十足类/有十脚的/ | decapsulation /无套模/被膜剥脱术/

polisher：抛光机

参加对象:可以很好的进行汽车空军1号车漆被膜操作,有过用抛光机(polisher)操作的经验. 因为掌握汽车空军1号车漆被膜的基本操作是参加的基本条件之一,所以我们在培训前将对参加者的技术水平进行确认.

tunica：膜

tungstyl /钨氧基/ | tunica /膜/ | tunicate /有被膜的/有被囊的/

tunicate：有被膜的

tunic 束腰外衣 | tunicate 有被膜的 | tunicle 法衣

tunicate：有被囊的

有被膜的tunicate | 有被囊的tunicate | 有壁细胞lepocyte

tunicate：有被膜的/有被囊的

tunica /膜/ | tunicate /有被膜的/有被囊的/ | tunicle /法衣/

tunicle：法衣

tunicate 有被膜的 | tunicle 法衣 | tuning fork 音叉

mesorchium：睾丸系膜

睾丸被腹膜的褶襞所包裹,覆盖其表面的部分形成生殖上皮,与腹腔壁连结的部分形成睾丸系膜(mesorchium). 在哺乳类生殖上皮的下面,有结实的结缔组织的白膜(tunica albuginea),睾丸实体被睾丸小隔(sep-tula)分隔成许多小叶.

encapsulated ending：有被末梢

encapsulated 有膜的 | encapsulated ending 有被末梢 | encapsulated larva 被囊蚴