RELATION BETWEEN THE ACROSOME REACTION AND FERTILIZATION IN THE SEA URCHIN. II. FERTILIZATION IN ACIDIFIED SEA WATER WITH EGG-WATER-TREATED SPERMATOZOA*

Fertilization of sea urchin eggs fails to occur at a pH lower than 6.5. Analytical studies on this problem were made with Hemicentrotus pulcherrimus, Anthocidaris crassispina and Pseudocentrotus depressus. If the spermatozoa have been pretreated with egg water, eggs can be fertilized even at pH 6.5 and 6.0. The acrosome reaction is inhibited at a pH lower than 6.5. Intact spermatozoa fail to adhere to the fixed eggs in acidified sea water, whereas egg-water-treated spermatozoa adhere even at pH 6.5 and 6.0. From these results we infer that the failure of fertilization at pH 6.5–6.0 is caused by non-occurrence of the acrosome reaction, and that fertilization reactions other than the acrosome reaction, such as the binding and fusion of the gametes, are not inhibited in this range of pH. At pH 5.5, the spermatozoa become inert and fertilization is inhibited or suppressed, even though egg-water-treated spermatozoa are employed.     

EFFECT OF TRYPSIN ON THE FERTILIZING CAPACITY OF SEA URCHIN SPERMATOZOA TREATED WITH EGG-WATER*

The effect of trypsin on the fertilizing capacity of spermatozoa was studied with 6 species of sea urchins. Trypsin has no harmful effect on intact spermatozoa. However, spermatozoa which have undergone the acrosome reaction in egg-water lose the fertilizing capacity when treated with trypsin-sea water. Electron- microscopical examination revealed that trypsin does not produce any morphologically noticeable effect on intact spermatozoa, but does dissolve the material covering the acrosomal tubule of the spermatozoa which have undergone the acrosome reaction. It is likely that the loss of this material is closely correlated with the loss of fertilizing capacity of spermatozoa by the trypsin treatment.     

Induction of the Acrosome Reaction of Sea Urchin Spermatozoa by Means of Urea

Urea is an effective reagent for inducing the acrosome reaction of spermatozoa in sea urchins. Urea-treated spermatozoa are capable of fertilizing eggs in Ca-deficient sea water. The pH of the urea solution is an important factor affecting the induction of the acrosome reaction. The reaction occurs at a high percentage in urea Solution at pH's higher than 7.8, while the reaction is almost completely suppressed at pH 7.2. Ca⁺⁺ is also an important factor for the induction of the reaction, although the minimum concentration required is very low.
The acrosomal filament formed in urea solution is similar in shape to that formed in egg-water, when fixed after 10 seconds' urea-treatment. The acrosome granule material is found around the basal portion of the acrosomal filament.     

Importance of Queen Bumble Bees as Pollinators Facilitating Inter-morph Crossing in Primula sieboldii

Abstract Flower-visiting insects, the distribution of pollen on an insect's body, and fruit and seed sets of Primula sieboldiiE. Morren were investigated in a maritime deciduous forest habitat of the Hidaka region in Hokkaido. Queens of Bombus diversus tersatus Smith (Hymenoptera: Apidae), Bombus schrencki albidopleuralis Skorikov, and Bombus deuteronymus deuteronymus Schulz were observed to visit the flowers of the species. Bumblebee claw marks were found on the flower petals of 68% of the flowering ramets of the species. Scanning-electronmicroscopy revealed that pin and thrum pollens of P. sieboldii were deposited in different positions along the proboscis of a B. diversus tersatus queen (n=38400 grains). On the glossa, all the observed pollen was of the pin type, while more than half of the pollen grains observed on the upper part of the proboscis, galea, stipes, and maxillary palpus were of the thrum type. In the field, high fruit and seed sets were recorded for both pin and thrum morphs, indicating the occurrence of sufficient legitimate pollination during the flowering season. In addition to the effectiveness of queen bumblebees as pollinators for P. sieboldii suggested in this study, phenological and morphological matches, i.e., early spring flowering during the queen bee emergence season and the similar lengths of the corolla tube and the bee proboscis, also support the inference that queen bumble bees play an important role in legitimate pollination of P. sieboldii.     

Lactate Dependent Protein Synthesis in Round Spermatids from Rat Testes

Lactate (20 mM) markedly increased protein labeling of round spermatids (steps 1–8) from rat testes. The stimulatory effect of lactate on protein labeling was also observed to some degree in spermatocytes and late spermatids (steps 13–16), but not in Leydig cells and 7 day-old testis cell suspznsions. In the lactate-treated spermatids, 51 % of the labeled proteins was found in the water-soluble fraction (the 105,000 × g 1 hr supernatant), whereas only 21%, in the control cells. The labeled proteins did not break down for at least 90 minutes in the presence of lactate. Actinomycin D (20 μg/ml) had no effect on [³H]leucine incorporation into the water-soluble proteins of spermatids, while labeling of the water-insoluble proteins (the 105,000 × g 1 hr pellet) was decreased by 23%.
These findings suggest that the round spermatids might be the most susceptible for the lactate-induced stimulation of protein synthesis among various types of testicular cells, and that lactate increases the synthesis of water-soluble proteins which may be regulated in the translational level of protein synthesis.     

Tea leaf peroxidase--Isolation and partial purification

Tea leaf peroxidase occurred as the insoluble form in a homogenate.A large part of the peroxidase from tea leaves was solubilizedin a homogenate by adding Tween-80. After fractionation by 0.3saturation with (NH₄)₂SO₄ and filtration of the homogenate througha Sephadex G-25 column, specific activity of the peroxidasein the effluent increased about 25 times. Crude peroxidase wasfractionated into six components; A-l, A-2, B-l, B-2, B-3 andC, by DEAE- and CM-cellulose column chromatography. The fractionsshowed different mobilities on disc gel electrophoregram atpH 4.2. An isoelectric focusing experiment indicated that pivalues of the A-l and A-2 components are 5.4 and 5.0, repsectively. ¹ Present address: National Institute of Agricultural Science,Ministry of Agriculture and Forestry, Nishigahara, Kita-ku,Tokyo, Japan. (Received October 19, 1970; )     

"EXTRANUMERARY" CUTICLE DEPOSITION IN PIECES OF LARVAL INTEGUMENT TRANSPLANTED TO A PUPA IN THE SILKWORM BOMBY X MORI

The author (K ato , 1973b) reported that in Bombyx mori , pieces of larval integument, if transplanted to a pupa, produced two layers of cuticle during the metamorphosis of the host pupa to an adult. In the present transplantation experiments, deposition of the two layers of cuticle was temporally examined to determine the timing of the two depositions, compared with the host's cuticle deposition, using 0-day-old fifth-instar or 1-day-old fourth-instar larvae as donors. In the transplant the first deposition occurred within 4 days of transplantation, with the second deposition at 6 to 8 days, while the host began cuticle deposition 6 days after receiving the transplant. These results show a failure of simultaneous deposition between the transplant and the host. These moulting events in the transplant, e.g. , the fairly early appearance of the first cuticle and temporally-separated ecdyses, are discussed in view of the change of ecdysone titer in the host. Furthermore, the temporal pattern of cuticle deposition in the transplant appeared to have a definite relationship with the type of cuticle deposited.     

Stage Depandent Inhibition of Plasmodiun falcipaium falciparum by Potent Ca2+ and Calmodulin Modulators

The effects Ca2+ channel blockers, verapamil, nicardipine and diltiazem, and of potent calmodulin (CaM) inhibitors, trifluoperazine (TFP), calmidazolium, W-7 and W-5, on Plasmodium falciparum in culture were examined. Among Ca2+ blockers, nicardipine was the most potent with the 50% inhibitory concentration (IC50) of 4.3 μM at 72 h after culture. Parasites were more sensitive to calmidazolium and W-7 with IC50 of 3.4 and 4.5 μM, respectively, than to TFP and W-5. All Ca2+ blockers and CaM inhibitors suppressed parasite development at later stages. Nicardipine, ditiazem, calmidazolium and W-5 also retarded parasite development at earlier stages and/or subsequent growth following pretreatment. Verapamil, nicardipine, TFP and calmidazolium reduced erythocyte invasion by merozoites. Fluroscence microscopy with the cationic flurescent dye rhodamine 123 revealed that nicardipine. TFP and calmidazolium depolarized both the plasma membrane and mitochondrial membrane potentials of the parasite. It is therefore considered that although al Ca2+ and CaM antagonists tested here influence parasite development at later stages, they are multifunctional, having effects not directly associated with Ca2+ channels or CaM.