Crystallization and some properties of cryptocytochrome c from aerobically-grown Pseudomonas denitrificans

1. 1. Analyses of cytochrome types in intact cells of aerobically-and anaerobically-grownPs. denitrificans indicated a higherratio of cytochrome c to cytochrome b in the former than inthe latter.
2. 2. Anaerobically-grown cells contained about twotimes as muchcryptocytochrome c as did aerobically-grown cells.
3. 3. Crystalline cryptocytochrome c obtained from the solublefraction of cell-free extracts of aerobically-grown cells manifestedthe same properties as cryptocytochrome c from anaerobically-growncells, i. e., absorption maxima, autooxidizability, redox potential,molecular weight, haem content, etc.
4. 4. Cryptocytochrome cwas reversibly converted to a true haemochrometype spectrumby alcohols, detergents, carboxylic acid salts,guanidine saltor high pH values.

(Received December 16, 1968; )     

Tissue Distribution of an Immunogenic Melanoma Associated Antigen,D-1

A human melanoma-associated antigen immunogenic in patients was recently identified by screening an expression cDNA library constructed from cultured human melanoma cell line with sera from patients with melanoma. The nucleic acid sequence of the cloned D-1 cDNA has no significant homology with previously reported mammalian genes. The cDNA D-1 encodes a peptide of about 37 kDa, which showed fivefold higher reactivity with sera from patients with melanoma than with sera from normal donors. In order to detect D-1 gene expression in vivo, in-situ hybridization and immunostaining with cRNA probe and murine anti-D-1 sera were carried out on surgically removed tissues. Digoxigenin-labeled cRNA D-1 was exclusively hybridized with mRNA in the cytoplasm of melanoma cells but not with keratinocytes and fibroblasts adjacent to melanoma nests. Polyclonal anti-D-1 antibodies were obtained by immunization of Balb/c mice with recombinant D-1 peptide and clearly reacted with melanoma cells but not with keratinocytes and fibroblasts, similar to the results of in-situ hybridization. The above information will help to assess the suitability of recombinant D-1 peptide to implement active specific immunotherapy in patients with melanoma.     

A kinetic analysis of cadmium accumulation in a Cd hyper‐accumulator fern,Athyrium yokoscense and tobacco plants

Cadmium (Cd) accumulations in a Cd hyper‐accumulator fern, Athyrium yokoscense (Ay), and tobacco, Nicotiana tabacum (Nt), were kinetically analysed using the positron‐emitting tracer imaging system under two medium conditions (basal and no‐nutrient). In Ay, maximumly 50% and 15% of the total Cd accumulated in the distal roots and the shoots under the basal condition, respectively. Interestingly, a portion of the Cd in the distal roots returned to the medium. In comparison with Ay, a little fewer Cd accumulations in the distal roots and clearly higher Cd migration to the shoots were observed in Nt under the basal condition (maximumly 40% and 70% of the total Cd, respectively). The no‐nutrient condition down‐regulated the Cd migration in both species, although the regulation was highly stricter in Ay than in Nt (almost no migration in Ay and around 20% migration in Nt). In addition, the present work enabled to estimate physical and physiological Cd accumulation capacities in the distal roots, and demonstrated condition‐dependent changes especially in Ay. These results clearly suggested occurrences of species‐/condition‐specific regulations in each observed parts. It is probable that integration of these properties govern the specific Cd tolerance/accumulation in Ay and Nt.     

CHANGES IN ACTIVITIES OF CREATINE KINASE, ARGININE KINASE AND THEIR MULTIENZYME FORMS DURING EMBRYONIC AND LARVAL DEVELOPMENT OF SEA URCHINS

The presence and the changes of CPK and APK have been studied during larval development through metamorphosing of Hemicentrotus pulcherrimus, Anthocidaris crassispina and Pseudo-centrotus depressus . While no CPK activity was found in the unfertilized eggs and the embryos of early developmental stages, APK was quite active throughout these stages. At the late 8-armed pluteus stage just prior to metamorphosis, CPK first became active. Electrophoretically this CPK was identical with one of three CPK forms of sperm, tube feet and esophagus but not with two CPK forms of lantern muscle. APK in the unfertilized eggs and early embryos was electrophoretically separated into two distinct molecular forms, one of which disappeared during the late larval stages. The persisting form of larval APK was identical with a single APK form present in the adult muscular tissues.     

LACTATE OXIDATION SYSTEM IN ACETOBACTER SUBOXYDANS, WITH SPECIAL REFERENCE TO CARBON MONOXIDE-BINDING PIGMENT

1. Lactate oxidation system was investigated in Acetobacter suboxydans,which was found to have cytochromes a and b, but no cytochromec. Haemoprotein 558 was also found to exist.
2. Carbon monoxideinhibited the lactate oxidation in the darkbut not in the light.WARBURG'S partition constant was estimatedto be 7.
3. Additionof haemoprotein 558 noticeably enhanced the oxygenuptake bythe LDH preparation, which was obtained from bacterialcellsand partially purified.
4. Haemoprotein 558 has protohaem asits prosthetic group. Notonly its absorption spectrum is reminiscentof that of peroxidase,but it also shows peroxidase-like reactivitywith some ligandswith a few exceptions.
5. Ferrohaemoprotein558 reacts with oxygen, forming, at first,a complex, whichhas its SORET absorption peak at 423 mµ.The absorptionmaximum then shifts to 417 mµ, indicatinga transformationto another compound. One of these two productsis likely tobe the oxygenated ferro-haemoprotein 558.
6. The mutual transformationbetween cytochrome B and haemoprotein558 is discussed.

(Received October 8, 1965; )     

Changes in Sugar Content during Cold Acclimation and Deacclimation of Cabbage Seedlings

The relationship between freezing tolerance and sugar contentin cabbage seedlings was investigated. Seedlings exposed tonon-freezing low temperature (5 °C) acquired freezing tolerancedown to -6 °C. The degree of freezing tolerance increasedwith duration of exposure to low temperature (up to 10 d). Sucrose,glucose, fructose and myo -inositol were detected as solublesugars in cabbage leaves, and all soluble sugars, except formyo -inositol, and starch increased gradually during cold acclimationsuch that their levels were positively correlated with the degreeof freezing tolerance. The induced freezing tolerance was attributednot to ontogenetic changes but to cold acclimation. However,the induced freezing tolerance was lost after only 1 d of deacclimationat control temperatures, and this change was associated witha large reduction in sugar content. These results reveal that the sugar content of cabbage leavesis positively correlated with freezing tolerance. Brassica oleracea L.; cabbage; cold acclimation; deacclimation; freezing tolerance; sugars