Formations of Extracellular Isoamylase and Intracellular α-Glucosidase and Amylase(s) by Pseudomonas SB15 and a Mutant Strain

Pseudomonas SB15, which produces extracellular isoamylase, was found to produce intracellular alpha-glucosidase and amylase(s) when grown on maltose. A mutant strain (MS1) derived from it, which formed isoamylase constitutively, also produced these intracellular enzymes constitutively. The activities of the enzymes produced in the mutant strain were much greater than those induced in the parent strain.     

Preliminary crystallographic study of a ribulose-1,5-bisphosphate carboxylase-oxygenase from Chromatium vinosum

Crystals of a ribulose-1,5-bisphosphate carboxylase-oxygenase from Chromatium vinosum were obtained with the hanging-drop vapor diffusion technique, using polyethylene glycol 4000 as precipitant. The crystal belongs to the cubic system, space group I432, with unit cell dimension a = 245.9 A. An asymmetric unit includes one-quarter (L2S2, L: large subunit, S: small subunit) of a hexadecameric molecule (L8S8, 544,000 Mr), which is located on the crystallographic point symmetry 222 or 4. The crystal diffracts to at least 3.0 A resolution.     

A sensitive assay of GTP cyclohydrolase I activity in rat and human tissues using radioimmunoassay of neopterin

A highly sensitive and simple assay for the activity of GTP cyclohydrolase I (EC 3.5.4.16) was established using a newly developed radioimmunoassay. D-erythro-7,8-Dihydroneopterin triphosphate formed from GTP by GTP cyclohydrolase I was oxidized by iodine and dephosphorylated by alkaline phosphatase to D-erythro-neopterin, and quantified by a radioimmunoassay for D-erythro-neopterin. This method was highly sensitive and required only 0.2 mg of rat liver tissues for the measurement of the activity. It was reproducible and can be applied for the simultaneous assay of many samples. The activity of GTP cyclohydrolase I was measured in several rat tissues. For example, the enzyme activity in rat striatum (n = 5) was 13.7 +/- 1.5 pmol/mg protein per hour (mean +/- SE), and agreed well with those obtained by high-performance liquid chromatography with fluorescence detection. The activity in the autopsy human brains (caudate nucleus) was measured by this new method for the first time. The activity in the caudate nucleus from parkinsonian patients (n = 6) was 0.82 +/- 0.56 pmol/mg protein per hour which was significantly lower than the control value, 4.22 +/- 0.43 pmol/mg protein per hour (n = 10).     

Phenotyping of malignant hematopoietic cells. Analysis of 1200 cases of leukemia-lymphoma

1255 cases of leukemia-lymphoma were tested between 1972 and 1984 by multiple marker analysis. Routine leukemia phenotyping was performed using standard morphological and cytochemical techniques in combination with clinical and histo-pathological information; the main emphasis was put on immunological surface marker analysis using erythrocyte rosette assays, TdT and a large panel of poly- and monoclonal antibody tests. The 1255 cases were divided into these major types and subtypes: 349 cases of ALL and related immature T- and Burkitt-lymphomas (cALL, pre B-ALL, B-ALL and Burkitt-lymphomas, T-ALL and immature, mostly leukemic T-lymphomas, Null-ALL), 454 cases of mature T- and B-cell malignancies (T-CLL, mycosis fungoides, Sezary-syndrome, T-lymphomas, B-CLL, hairy cell leukemia, multiple myeloma, B-lymphomas), 263 cases of acute myeloid leukemias (AML, AMMoL/AMoL), 182 cases of chronic myeloid leukemias (CML in chronic phase, CMoL, CML in blast crisis), 6 cases of erythroleukemia and 1 case of megakaryoblastic leukemia. A simplified classification scheme which has been used in our laboratories is presented. Phenotyping is of diagnostic, prognostic and therapeutic relevance, most evidently for patients with ALL. Routine leukemia phenotyping should be performed with highly standardized techniques and reagents and by combining information from several fields in the multiple marker analysis. New areas of leukemia research might become very useful for the routine procedure of phenotyping.     

Glucocorticoids suppress and oestrogens enhance the lipopolysaccharide-induced increase in putrescine and N1-acetylspermidine in mouse liver

Previously we reported that administration of lipopolysaccharide (LPS) to mice increased the hepatic levels of putrescine (PUT) and N¹-acetylspermidine (N¹-acetyl-SPD). In the current study, we examined the in vivo effects of some steroid hormones on the LPS-induced increase in PUT and N¹-acetyl-SPD. Corticosterone, hydrocortisone and dexamethasone suppressed the LPS-induced increase in PUT and N¹-acetyl-SPD in mouse liver in a dose-dependent manner, dexamethasone being the most effective among them. On the other hand, oesterone and oestradiol-17β enhanced the LPS-induced increase in PUT and N¹-acetyl-SPD in a dose-dependent manner. Oestradiol-17 and 16β-ethyl-oestradiol, as an inactive oestradiol isomer and an antioestrogen, respectively, likewise enhanced the increase in PUT and N¹-acetyl-SPD concentrations induced by LPS. 16-hydroxy-oestradiol (oestriol), 16-hydroxyestrone, 2-hydroxyoestradiol, 2-hydroxyoestrone, progesterone, testosterone, diethylstilboestrol and nonsteroidal antioestrogen such as tamoxifen and nafoxidine had no effect on the increase. Oestradiol-17β enhanced and corticosterone had little on the carbon tetrachloride-induced increase in PUT and N¹-acetyl-SPD. These results suggest that glucocorticoids suppress the increase by preventing the immunological injury by Kupffer cells on hepatocytes and that the stimulatory effect of oestrogens may not be associated with their oestrogenic activities mediated by the oestrogen receptor system.     

Foraging for patchily-distributed leaf-miners by the parasitoid,Dapsilarthra rufiventris (Hymenoptera: Braconidae). II. Stopping rule for host search

We studied the stopping rule which the female parasitoid,Dapsilarthra rufiventris, uses for deciding when to leave the leaflet on which she is searching for leaf-mining larvae,Phytomyza ranunculi. She is unlikely to employ some current stopping rules, such as fixed-number and fixed-time rules and others. The searching female appears to deposit a marking pheromone on the leaflet. We formulated a model for predicting the amount of pheromone accumulated on the leaflet. The model assumes that she will deposit the pheromone on the leaflet at a given rate (a) per unit time which is proportional to search speed, and will leave it when the amount of pheromone reaches the thresholdL. In this modelL denotes the amount of the search effort spent on the leaflet. The model was fitted fairly well to the data. A comparison of the observed results with the predictions of the model suggests thatL increases markedly at the first encounter with the mine and at a lower rate for the subsequent encounters. This appears to be a kind of area-concentrated search, that is, searching for hosts for a while in the immediate vicinity after finding one host, and would be adaptive in foraging forP. ranunculi larvae, which exhibit clumped distributions among leaflets in the field.     

Studies on ecology and behavior of Japanese black swallowtail butterflies. 6. Nectar feeding ofPapilio helenus nicconicolens Butler andP. protenor demetrius Cramer as main pollinators of glory bower,Clerodendron trichotomum,Thunb

The butterfliesPapilio helenus andP. protenor were shown to feed mainly on the nectar of the glory bower,Clerodendron trichotomum, which was the most abundant nectar plant in summer in the study area. Both the species were found to have a proboscis longer than 24 mm corresponding to the length of the corolla tube ofC. trichotomum. Visits to the flowers by these butterflies were observed more frequently than visits by sphingid moths which had previously been believed to be the major pollinators ofC. trichotomum. The male butterflies visited trees ofC. trichotomum frequently, while visits by the females were less frequent. However, once females had visited the tree ofC. trichotomum, they remained there longer than the males. Since the flower ofC. trichotomum has long protruding sexual organs, its pollen grains were found to adhere efficiently to the bodies of butterflies, mainly the thorax, during nectar feeding. Most of the butterflies became loaded withC. trichotomum pollen, and the mean number of pollen grains per butterfly was 1,776 forP. helenus and 2,817 forP. protenor. The flowers opened at any time of day but more frequently in the morning. The nectar was secreted throughout the day. In the maturation of the protandrous flower ofC. trichotomum, the duration of the pistillate phase was about twice as long as the staminate phase. The long flowering period and the short duration of the staminate phase resulted in asynchrony of the flowering stages even within a single cyme on a tree. Such asynchrony and the abundance of attractive flowers on a tree facilitates efficient pollination by the butterflies.     

Blood clotting factor IX Niigata: substitution of alanine-390 by valine in the catalytic domain

Factor IX Niigata is a mutant factor IX responsible for the moderately severe hemophilia B in a patient who has a normal level of factor IX antigen with reduced clotting activity (1-4% of normal). We reported previously that the purified mutant protein could be converted to the factor IXa beta form by factor XIa/Ca2+ at a rate similar to that in the case of normal factor IX, but the resulting mutant factor IXa beta could not activate factor X in the presence of factor VIII, Ca2+, and phospholipids (Yoshioka, A. et al. (1986) Thromb. Res. 42, 595-604). In the present study, we analyzed factor IX Niigata at the structural level to elucidate the molecular abnormality responsible for the loss of clotting activity. Amino acid sequence analysis of a peptide obtained on lysyl endopeptidase digestion, coupled with subsequent SP-V8 digestion, demonstrated that the alanine at position 390 was substituted by valine in the catalytic domain of the factor IX Niigata molecule.