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51.
52.
Summary Spermatozoa from fertile and infertile human ejaculates were observed under the scanning electron microscope. A parallel study of sections was performed by transmission electron microscope.The normal head shows under the scanning electron microscope vesicular elevations in the region of the acrosome and a smooth and rigid appearance corresponding to the postnuclear cap whose occurrence is confirmed under the transmission electron microscope. Immediately anterior to this cap a shallow furrow transverses the head. Duplicated, unusually large or small and deformed heads are found under the scanning electron microscope. Most of these abnormal heads show no surface structure suggesting an acrosome.The neck and middle piece are occasionally, though frequently in abnormal spermatozoa, covered by a cytoplasmic droplet. Otherwise, the mitochondrial sheath is recognized under the scanning electron microscope as a beaded thickening in the middle piece. The lack of mitochondria is manifested by a smooth middle piece thinner than the principal portion. Transmission electron microscopy of sections reveals various types of anomalies in the number of cores, core filaments and mitochondria embedded in the cytoplasmic droplets.Abnormalities in the principal portion of the tail such as duplication, unusual thickness and length are shown under the scanning electron microscope.The investigation indicates that scanning electron microscopy is suited for the clinical as well as cytological examination of human ejaculate spermatozoa. 相似文献
53.
54.
Makoto Suematsu Shigenari Houzawa Soichiro Miura Hiroshi Nagata Tetsuji Kitahora Tetsuo Morishita Chikara Oshio Masaharu Tsuchiya 《Luminescence》1989,4(1):531-534
Reaction difference of oxyradical generation and luminol-dependent photoemission of zymosan- and phorbol ester-treated neutrophils were investigated using a conventional photomultiplier and ultrasensitive photonic imaging technique. Zymosan-treated cells released a concentrated photonic burst corresponding to the cellular distribution. In contrast, phorbol ester-treated cells produced a negligible level of photoemission, and the additional application of Ca2+ ionophore enhanced the photonic burst, which was gradually spread out into extracellular space. Serine protease inhibitors did not attenuate PMA-induced chemiluminescence but did attenuate zymosan-induced chemiluminescence. This suggests the involvement of serine protease in the respiratory burst of phagocytizing neutrophils. 相似文献
55.
To evaluate the influence of overwintering individuals of zooplankton on spring zooplankton communities, the dynamics of zooplankton
communities with or without overwintering individuals were observed in experimental ponds from fall to spring. An insecticide,
carbaryl, was used to regulate the overwintering individuals. In ponds which received insecticide applications in November
or January, all cladoceran and rotiferan species were eliminated by the treatments and did not reappear until late March or
early April, even when the chemical disappeared rapidly. The low water temperature may delayed the establishment of the populations
from resting eggs. In these ponds, populations of various cladoceran and rotiferan species, which seemed to be originated
from resting eggs, were built up in the spring. In control ponds,Daphnia ambigua orD. longispina overwintered as juveniles and adults and established a large spring population earlier than other cladocerans and rotifers
overwintering as resting eggs. The latter zooplankters did not increase in the spring probably because their growth was suppressed
by the precedingDaphnia species through competition. In nature, even if the number of overwintering individuals is small, they may have a potential
to build up a large population earlier than the individuals hatching from resting eggs. As a result, the species which have
overwintered as individuals seem to predominate in the spring and have a large influence on the spring zooplankton community. 相似文献
56.
Mariyo F. Watanabe Ken-Ichi Harada Kennji Matsuura Masayuki Watanabe Makoto Suzuki 《Journal of applied phycology》1989,1(2):161-165
Changes in the content of cyclic heptapeptide hepatotoxins called microcystins were investigated during batch culture of two
Microcystis species using high performance liquid chromatography. After adsorption to ODS-silica gel cartridges and elution with methanol,
the toxins were analyzed and quantified by HPLC. 35 μg per 100 mg dry cells of microcystin-RR, 34 μg of -YR and 43 μg of -LR
were present at the beginning of the exponential growth phase of M. viridis. Microcystin-RR increased markedly towards the end of the exponential phase with the maximum content of 112 μg per 100 mg
cells was measured at the late stage of the exponential phase. A remarkable increase of microcystin-YR from 130 μg per 100
mg cells to 1020 μg was observed during the exponential phase of a highly toxic strain of M. aeruginosa. However no clear differences were found in the pattern of change among the three toxins during the growth course. 相似文献
57.
Close linkage of MEN2A with RBP3 locus in Japanese kindreds 总被引:7,自引:0,他引:7
Masayuki Yamamoto Shin-ichiro Takai Tetsuro Miki Kazuyoshi Motomura Makoto Okazaki Isamu Nishisho Hideo Tateishi Akira Miyauchi Tasuku Honjo A. J. Pakstis Takesada Mori 《Human genetics》1989,81(3):287-288
Summary The gene responsible for multiple endocrine neoplasia type 2A (MEN2A) has recently been assigned to the pericentromeric region of chromsome 10 in European Caucasian kindreds by linkage analysis using a DNA marker, interstitial retinol-binding protein 3 (RBP3). We have found tight linkage between the MEN2A and RBP3 loci in Japanese MEN2A kindreds. The maximum lod score is 5.19 at a recombination fraction of 0.00. This result suggests that mutation of a certain gene close to RBP3 is responsible for MEN2A irrespective of ethnic backgrounds. 相似文献
58.
Studies on chemical synthesis of human cystatin A gene and its expression in Escherichia coli 总被引:1,自引:0,他引:1
A synthetic gene containing the coding sequence for the human cysteine proteinase inhibitor, cystatin A, was obtained by enzymatic assembly of 20 oligodeoxyribonucleotides which had been chemically synthesized by the solid phase phosphoramidite method. It was cloned into an Escherichia coli plasmid. The expression plasmid for cystatin A was constructed by introducing the synthetic gene downstream of the tac promoter of an E. coli plasmid which is a derivative of pKK223-3 with high copy number. The gene was expressed in E. coli JM109 without IPTG-induction. The expression of cystatin A was detected by SDS-polyacrylamide gel electrophoresis of the E. coli JM109 lysate, followed by immunoblotting using rabbit antiserum raised with human epidermal cystatin A and alkaline phosphatase-conjugated goat anti-rabbit IgG. The result showed that the molecular weight of the expression product is identical with that of the authentic protein and the antigenic properties are also the same. Furthermore, the expression product purified with a CM-papain Sepharose affinity column and FPLC system with a Mono-Q column showed the same inhibitory activity for various cysteine proteinases. Also, purified recombinant cystatin A was found to have identical amino acid composition, NH2-terminal amino acid sequence, and peptide-map on reverse phase HPLC with those of the authentic inhibitor. 相似文献
59.
K Hori Y Yamamoto T Minetoki T Kurotsu M Kanda S Miura K Okamura J Furuyama Y Saito 《Journal of biochemistry》1989,106(4):639-645
The entire gene for gramicidin S synthetase 1 (GS 1) was cloned into the plasmid vector pUC18, and the nucleotide sequences of the GS 1 gene and its flanking region were determined. The full-length clone was 4,539 base pairs long and had an open reading frame of 3,294 nucleotides coding for 1,098 amino acids. The calculated molecular weight of 123,474 agreed with the apparent molecular weight of 120,000 found in SDS-PAGE of GS 1 from B. brevis. The nucleotide sequence of GS 1 gene was highly homologous to that of tyrocidine synthetase 1. The overall similarity between the deduced amino acid sequences of the two genes was 57.5%. The gene product of clone GS309 was easily purified to an essentially homogeneous state by ammonium sulfate fractionation followed by DEAE-Sepharose CL-6B, Ultrogel AcA-34, and second DEAE-Sepharose CL-6B column chromatography. The purified protein catalyzed the D-phenylalanine-dependent ATP-32PPi exchange reaction which is specific for GS 1 activity, and the specific activity of the purified product was nearly the same as the purified GS 1 from B. brevis. The product also showed a weak phenylalanine racemase activity. 相似文献
60.
Masayuki Nakamichi Fumiaki Cho Tetsuhiro Minami 《Primates; journal of primatology》1990,31(2):213-224
This study documents age-related changes in the interactions of wild-born cynomolgus macaque mothers and their infants living
in individual cages during the first 14 weeks of infant life. Body contact between mother and infant, maternal holding, and
infant sucking were found to decrease, and the mothers showed an increased frequency of aggression toward their infants with
age. These results were broadly similar to those reported for mother-infant interactions in other macaques living in social
groups. Nevertheless, a clear difference between the present cynomolgus macaques and other macaques in social groups was apparent.
The cynomolgus macaque mothers tended to permit their infants to move about freely without displaying maternal protectiveness
such as restraint or retrieval, unlike other macaque mothers in social groups. Such maternal behaviors might derive from the
experience of living in individual cages for many years and the relative safety of living in individual cages. The lack of
maternal restraint and retrieval could be responsible for the observed sex differences in behavior: male infants moved more
actively, and broke, and made contact with their mothers more frequently than did female infants. Moreover, mothers of female
infants held and groomed them more frequently and were less aggressive toward them. 相似文献