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The thread-like apparatus and its movement are observed clearlywith a phase contrast microscope, as shown in the photomicrographs.When caffeine solution is used as a medium, the thread-likeapparatus and the tannin vacuole have a precipitation in them.There is some degree of caffeine reaction in these threads. A part of the thread-like apparatus assumes a bead-like formor a small mass, and the rest of the thread becomes long andslender. Tiny granules are observed near thread-like apparatuseswith a phase contrast microscope, but these granules cannotbe revealed with vital staining. The vermiculation of the thread-like apparatus is slower nearthe nucleus than in the vicinity of chloroplasts. Generallyspeaking, the movement of the thread within the living cellcan be said to be marked.
1Dedicated to Prof, Hajime MATSUURA and Prof. Yukio YAMADA celebratingtheir sexagenary birthdays. Contribution No. 32 from the BiologicalSection, Tokyo Woman's Christian College. (Received May 14, 1960; ) 相似文献
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Benzyladenine (BA) was applied to intact bean (Phaseolus vulgaris) leaves at different stages of their growth. Changes in the amounts of cellular constituents resulting from the different treatments were followed and compared. RNA, protein, and chlorophyll contents, dry weight, fresh weight, and leaf area per single leaf continued increasing when leaves were treated with BA from an early stage, whereas in untreated leaves all these values levelled off or declined with advancing age. Besides these changes, BA treatment induced an increase in the DNA content. Changes in RNA content was more remarkable in response to application or deprival of BA treatment than the corresponding ones in protein and chlorophyll contents. The pattern of response to BA varied greatly according to the age at which the leaf received the treatment. As leaves aged, they lost the ability to increase their area and fresh weight in response to BA. However, continuous treatment with BA from an early stage kept the leaves young and able to respond. 相似文献
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Sperm-egg interaction during normal fertilization in the sea urchins, Strongylocentrotus intermedius and Hemicentrotus pulcherrimus, was studied by scanning and transmission electron microscopy. Several seconds after insemination, acrosome-reacted spermatozoa were found attached to the surface of the vitelline coat on each egg. Soon, several bulges of the vitelline coat appeared surrounding the fertilizing spermatozoon. These bulges then spread over the surface increasing in number, while they became fewer and disappeared around the sperm head. Thin sections of the bulging areas revealed discharging cortical granules. As the bulging vitelline coat was elevated, the sperm head was incorporated into the perivitelline space, passing through a small hole in the coat that resulted from penetration of the sperm acrosomal process immediately before fusion of the gametes. When the spermatozoon disappeared beneath the fertilization membrane, a hole was left in the membrane and the cortical reaction had finished on the other hemispheric surface. Mechanical removal of the membrane at that time exposed a spermatozoon protruding perpendicularly from the egg plasma membrane surface. The anterior tip of the sperm head was smoothly connected with the egg surface, and neither microvillous projections nor cytoplasmic covering of the egg cytoplasm could be found around the spermatozoon. 相似文献
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MASAHIRO FUJISHIMA HIDEO DOHRA MIKI KAWAI 《The Journal of eukaryotic microbiology》1997,44(6):636-642
ABSTRACT. The Gram-negative bacterium Holospora obrusa is a macronucleus-specific symbiont of the ciliate Paramecium caudatum. The infectious form of this bacterium infects the host macronucleus through digestive vacuoles and differentiates into the reproductive form two days after the infection in the nucleus. The monoclonal antibodies IF-3–1 and IF-3–2 reacted with 39 and 1S kDa periplasmic proteins, respectively, that were specific for the infectious form of H. obrusa. Because the antigens were not detected in the reproductive form of the bacterium, it appears that expression of the proteins decreases during or soon after the infection. Using these antibodies, quantitative changes in the antigens in the early infection process were examined by immunoblotting and immunogold electron microscopy. Immunoblotting showed that the amounts of both antigens were reduced within 1 h after the bacteria were engulfed into the digestive vacuoles of the paramecia, but that the amounts of IF-3–2 antigens declined earlier than the IF-3–1 antigen. Immunogold labeling showed that the level of IF-3–2 antigens became very low in the bacteria in the host digestive vacuoles, whereas there was no similar decrease in amount of IF-3–1 antigens. Possible functions of the antigens are discussed. The IF-3–1 antigens decrease in concentration in parallel with the decrease in the periplasmic region. 相似文献
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The blastomeres isolated from urodelan blastulae continued to divide without aggregating of daughter cells when inoculated with Ca2+-free neutral Holtfreter solution into glass culture dishes coated with agar. When standard Holtfreter solution with pH 8.2 was used as a culture medium, Ca2+ content from 1/40 to 1/20 of the original strength was essential for the purpose of the present observations; other divalent cations such as Mg2+, Ba2+ or Mn2+ replaced Ca2+. Under these experimental conditions, cell pedigrees were obtained during the incubation period. The greatest number of cell divisions so far observed in vitro was 8 for Hynobius lichenatus, and 9 for Cynops pyrrhogaster. Some related observations on the behavior of isolated blastomeres are also presented. 相似文献
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KAORU NIKI KATSUTOSHI YOSHIZATO HIDEO NAMIKI SAKAÈ KIKUYAMA 《Development, growth & differentiation》1984,26(4):329-338
DERBY successfully maintained the tail of tadpole ( Rana pipiens) in vitro over a period of 2 weeks in a physiological salt solution (1). When we tried to apply DERBY'S methods of the tissue culture to tadpoles of bullfrog, Rana catesbeiana , it was found that the tissue regressed spontanously without stimulation of thyroid hormone. Several different media were examined in order to select a better culture medium for the bullfrog tadpole tissues. RPMI-1640 medium supplemented with insulin and transferrin was found to be satisfactory for this aim. With this improved medium, the interaction between the epidermis and the mesenchyme has been investigated during the hormone-induced tadpole tail regression and the epidermal dependence of the mesenchyme regression was demonstrated by the following three experiments. (i) Some of surgically prepared mesenchymes regressed in responce to thyroid hormone. In these cases the mesenchymes were revealed to be contaminated with the remaining epidermal cells. (ii) Complete removal of the epidermis was accomplished by the chemical treatment. The mesenchyme thus obtained ("nude tail fin") was insensible to thyroid hormone. (iii) "Skin conditioned medium" (SCM) was prepared by culturing the skin in the presence and absence of thyroid hormone. Nude tail fin regressed when cultured in the SCM containing thyroid hormone. 相似文献
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Primary leaves of intact bean plants (Phaseolus vulgaris L.) were treated with benzyladenine (BA) at different stages during growth. Changes in DNase, RNase, and proteas activities in the leaves were followed. Unlike the case of various excised tissues, cytokinin raised the activities of these hydrolases in intact bean leaves. Because BA elevated the levels of DNA, RNA, and protein in intact leaves, it may stimulate both synthesis and decomposition of these cellular constituents. The hydrolase activities showed differential responses to BA according to the age at which the leaf received the hormone treatment. 相似文献
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<Emphasis Type="Italic">In vitro</Emphasis> Synthesis of tRNA<Superscript>Tyr</Superscript> Precursors and their Conversion to 4S RNA 总被引:3,自引:0,他引:3
HIDEO IKEDA 《Nature: New biology》1971,234(50):198-201
Three bacterial-specific RNA messengers, transcribed in vitro from phage ?80psu3 DNA, contain the nucleotide sequence corresponding to the tRNATyr gene carried by this phage. As there is only one copy of this gene in the phage genome, there are thought to be three promoter sites on the DNA template. 相似文献