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31.
32.
利用我们研制的厌氧培养皿及管,共检验了39份牙髓炎及牙周炎标本,分离出厌氧菌59株,标本中厌氧菌分离的阳性率为100%。其中类杆菌28株,消化链球菌9株,消化球菌7株,韦荣氏球菌5株,真杆菌2株,梭形杆菌8株。在类杆菌中产黑素类杆菌21株,占类杆菌总数的75%。结果表明使用厌氧培养皿及管研究厌氧菌简便、有效、经济,适于基层单位应用。 相似文献
33.
作者采用简单的螺胚生长抑制法,证明软体动物细胞具有DNA复制后修复功能,并受咖啡碱抑制。在没有其他诱变剂的参与下,咖啡碱并不损伤DNA,但也没有保护作用。 相似文献
34.
蚕豆根端细胞核中微核仁的研究 总被引:1,自引:0,他引:1
以蚕豆(Vicia faba)根端分生组织细胞为材料研究了微核仁的超微结构和细胞化学特点。结果表明;微核仁是直径0.3—0.5μm 的卵圆形或球形结构。常规染色时,微核仁与集缩染色质的电子密度相仿,但两者之间在结构上没有任何联系。细胞化学研究指出,微核仁含有 RNA 和蛋白质,其结构成分主要是与核仁颗粒组分十分相似的 RNP 颗粒。报道了植物细胞核中微核仁发生于核仁的过程并对微核仁的本质和功能进行了讨论。 相似文献
35.
云南西部狭臀蚤属四新种记述:蚤目:多毛蚤科 总被引:2,自引:1,他引:1
本文报告云南西部狭臀蚤属Steni(?)chia 4新种:1)金氏狭臀蚤,新种 S.chini sp.nov.与锐额狭臀蚤 S.angustifrontalis Xie et Gong接近;2)李氏狭臀蚤,新种 S.liae sp.nov.与金氏狭臀蚤新种和锐额狭臀蚤接近;3)柳氏狭臀蚤,新种 S.liui sp.nov.与李氏狭臀蚤新种和高山狭臀蚤S.montanis xie et Gong接近。4)吴氏狭臀蚤,新种 S.wui sp.nov.与卢氏狭臀蚤 S.lewis Smit接近。本文认论了李氏狭臀蚤新种与金氏狭臀蚤新种的形态分类及本属蚤类的宿主等生态问題,并编制本属14种的检索表。 相似文献
36.
Summary P-protein and the changes it undergoes after wounding of sieve tubes of secondary phloem in one- to two-year old shoots ofHevea brasiliensis has been studied using electron microscopy. The P-protein in the form of tubules with a diameter of 8–9 nm and a lumen of 2–2.5 nm occurred in differentiating sieve elements and appeared as compact bodies which consisted of small aggregates of the tubules. As the sieve elements matured, these P-protein bodies dispersed with a disaggregation of the tubules before they turned into striated fibrils, 10–11 nm in diameter. In wounding experiments, as the mature sieve elements collapsed after cutting, their striated P-protein converted into tubules. These tubules were the same in ultrastructure as the tubules in differentiating sieve elements and they often were arranged in crystalline aggregates. 相似文献
37.
38.
Targeting of glycoprotein I (gE) of varicella-zoster virus to the trans-Golgi network by an AYRV sequence and an acidic amino acid-rich patch in the cytosolic domain of the molecule. 总被引:10,自引:9,他引:1
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Previous studies suggested that varicella-zoster virus (VZV) envelope glycoproteins (gps) are selectively transported to the trans-Golgi network (TGN) and that the cytosolic domain of gpI (gE) targets it to the TGN. To identify targeting signals in the gpI cytosolic domain, intracellular protein trafficking was studied in transfected cells expressing chimeric proteins in which a full-length or mutated gpI cytosolic domain was fused to the gpI transmembrane domain and interleukin-2 receptor (tac) ectodomain. Expressed protein was visualized with antibodies to tac. A targeting sequence (AYRV) and a second, acidic amino acid-rich region of the gpI cytosolic domain (putative signal patch) were each sufficient to cause expressed protein to colocalize with TGN markers. This targeting was lost when the tyrosine of the AYRV sequence was replaced with glycine or lysine, when arginine was replaced with glutamic acid, or when valine was substituted with lysine. In contrast, tyrosine could be replaced by phenylalanine and valine could be substituted with leucine. Mutation of alanine to aspartic acid or deletion of alanine abolished TGN targeting. Exposure of transfected cells to antibodies to the tac ectodomain revealed that the TCN targeting of expressed tac-gpI chimeric proteins occurred as a result of selective retrieval from the plasmalemma. These data suggest that the AYRV sequence and a second signaling patch in the cytosolic domain of gpI are responsible for its targeting to the TGN. The observations also support the hypothesis that the TGN plays a critical role in the envelopment of VZV. 相似文献
39.
A study was undertaken to develop a protoplast regeneration system for pinellia. A yield of 19 29 x 105 protoplasts/g F. W. could be obtained from cell suspension cultures incubated in a digestion enzyme solution with 2% cellulase Onzuka R-10, 10% pectinase (Sigma), 0.01% pectolyase Y23. K8P and modified MS media were used to culture protoplasts in: a) liquid, b) liquid-solid double layer, or c) agarose embedded protoplast culture. The former two were conducive to colony formation from protoplast-derived cells. The frequency of cell division was about 8% after 3 days in culture. Gradually adding fresh medium of lower osmotic pressure into the medium for protoplast culture favored cell division. Calli (1–2 mm in diameter) formed after 30–40 days in culture. The calli transferred onto medium supplemented with KT (0.5 mg 1–1) and NAA (0.2 mg 1)–1) could regenerate plants after 40–50 days. Of 47 plantlets transplanted into plots, 29 flowered and were fertile.Abbreviations 2,4-D
2,4-dichlorophenoxyacetic acid
- NAA
-naphthaleneacetic acid
- KT
kinetin
- CH
casein hydrolysate 相似文献
40.
大鼠肝癌模型CBRH—3的建立及其生物学特性 总被引:8,自引:0,他引:8
用DENA诱发近交系Wistar大鼠,经三个月后得原发性肝癌,移植于同品系幼鼠,从而建立了 一株染色体众数正常,AEP阳性的大鼠移植性肝癌模型,命名为CBRH-3,病理鉴定为肝细胞型肝 癌。至今已传至60余代,目前生长稳定。 相似文献