Cloning and characterization of genes encoding an enzyme which oxidizes dimethyl sulfide in Acinetobacter sp. strain 20B

Acinetobacter sp. strain 20B was isolated based on the ability to utilize dimethyl sulfide as the sole sulfur source. Since strain 20B oxidized indole as well as dimethyl sulfide, indigo production by recombinant Escherichia coli clones carrying Acinetobacter DNA was used as a selection for cloning genes encoding dimethyl sulfide oxidation genes. The gene encoding an indole-oxidizing enzyme was also found to oxidize dimethyl sulfide. The dimethyl sulfide-oxidizing enzyme genes consisted of six open reading flames designated dsoABCDEF. The deduced amino acid sequences of dsoABCDEF were homologous with those of the multicomponent phenol hydroxylases. DsoABCDEF oxidized dimethyl sulfide to dimethyl sulfoxide, and dimethyl sulfoxide to dimethyl sulfone.     

Glucose tolerance disorders in individuals chronically exposed to carbon disulfide (CS2)

An incidence of glucose tolerance disorders was investigated in the group of 47 employees of the viscose fibres of the mean duration of exposition exceeding 20 years. Control group included 31 employees uniform in the age and body weight. Carbohydrate metabolism was tested with the oral load with 100 g of glucose and intravenous glucose administration according to Conrad. Glucose tolerance disorders were noted in 11 employees (23.4%) chronically exposed to CS2 in the concentrations slightly exceeding acceptable levels whereas glucose intolerance was noted in 2 individuals (6.5%) of the control group. The difference was statistically significant. No difference in the glucose absorbability index was noted. Exposition time to the studied CS2 concentrations did not affect the incidence of the glucose tolerance disorders.     

Physiology, biochemistry and taxonomy of deep-sea nitrile metabolising Rhodococcus strains

A collection of nitrile-hydrolysing rhodococci was isolated from sediments sampled from a range of deep coastal, and abyssal and hadal trench sites in the NW Pacific Ocean, as part of our programme on the diversity of marine actinomycetes. Nitrile-hydrolysing strains were obtained by batch enrichments on nitrile substrates with or without dispersion and differential centrifugation pre-treatment of sediments, and were recovered from all of the depths sampled (approximately 1100–6500 m). Two isolates obtained from the Ryukyu (5425 m) and Japan (6475 m) Trenches, and identified as strains of Rhodococcus erythropolis,were chosen for detailed study. Both of the deep-sea isolates grew at in situ temperature (4°C), salinities (0–4% NaCl) and pressures (40–60 MPa), results that suggest, but do not prove, that they may be indigenous marine bacteria. However, the absence of culturable Thermoactinomycespoints to little or no run off of terrestrial microbiota into these particular trench sediments. Nitrile-hydrolysis by these rhodococci was catalysed by a nitrile hydratase–amidase system. The hydratase accommodated aliphatic, aromatic and dinitrile substrates, and enabled growth to occur on a much wider range of nitriles than the only other reported marine nitrile-hydrolysing R. erythropolis which was isolated from coastal sediments. Also unlike the latter strain, the nitrile hydratases of the deep-sea rhodococci were constitutive. The possession of novel growth and enzyme activities on nitriles by these deep-sea R. erythropolisstrains recommends their further development as industrial biocatalysts.     

Mapping of the Glycoprotein 330 (Gp330) Gene to Mouse Chromosome 2

Glycoprotein 330 (Gp330) is a member of the low-density lipoprotein receptor gene family that is expressed in the kidney. We have mapped the Gp330 gene to mouse chromosome 2, 4.5 cM proximal to Acra, in an interspecific backcross of (C57BL/6J × Mus spretus) F1 × C57BL/6J.     

Properties of a microsomal enzyme system from Linum usitatissimum (linen flax) which oxidizes valine to acetone cyanohydrin and isoleucine to 2-methylbutanone cyanohydrin

Microsomal preparations from flax seedlings have recently been shown to convert L-valine to acetone cyanohydrin, the precursor of the cyanogenic glucoside linamarin [A. J. Cutler and E. E. Conn (1981) Arch. Biochem. Biophys. 212, 468-474]. Further details of this four-step biosynthetic sequence and also details of the analogous reactions in lotaustralin biosynthesis have been obtained. The lotaustralin precursor, 2-methylbutyraldoxime, is the best substrate for cyanide production (Vmax = 413 nmol h-1 g fresh wt-1) and inhibits the conversion of valine and isoleucine into products. Similarly, the linamarin precursor isobutyraldoxime is an excellent substrate (Vmax = 400 nmol h-1 g fresh wt-1) and also inhibits oxidation of the amino acids. The substrate specificity of the oxime-metabolizing step is low and a variety of aliphatic oximes are converted to cyanide. On the other hand, the activity of the microsomal extract is highly selective with regard to the amino acid substrate since, of the aliphatic amino acids tested, only valine and isoleucine are metabolized. We were unable to demonstrate product formation from isobutyronitrile (a linamarin precursor) but did observe detectable cyanide formation from 2-methylcyanobutane, the corresponding precursor of lotaustralin. Competition experiments showed that the biosynthesis of linamarin and lotaustralin is not likely to be catalyzed by separate enzyme systems.     

Ultrastructure and taxonomy of Paraphysomonas (Chrysophyceae) and related genera 2

This is the second of two accounts reporting on the occurrence and systematics of freshwater species of the colourless chrysophycean genus Paraphysomonas in the Cambridge area, using electron microscopy of whole mounts of both cells and scales and sections of scales. Twenty species are included here, eleven of which are new: P. cancellala, P. canistrum, P. homolepis, P. ignivoma, P. limbata, P. morchella, P. runcinifera, P. stelligera, P. stephanolepis, P. subquadrangularis and P. undulata. Five new subspecies are also established: P. circumvallata ssp. mediogranulata, P. poteriophora ssp. manubriata, P. punctata ssp. atrema , ssp. microlepis and ssp. simplicior. P. diademifera (Takahashi) comb. nov. [= Lepidochromonas diademifera (Takahashi) Kristiansen] has been included in Paraphysomonas since it has been found to be colourless and not pigmented as originally described and also to possess scales of a similar structure to those in other species of Paraphysomonas. One previously described species, P. inconspicua Takahashi, is here considered as a synonym of P. butcheri Pennick & Clarke. P. vacuolata Thomsen is removed from Paraphysomonas since it has been found to possess a chloroplast and will be included in a new genus in the third paper of this series. The 37 presently known species of Paraphysomonas have been arranged in 11 different groups according to similarities in scale structure. Consideration of the possible evolution of scale structure in Paraphysomonas and the possible interrelationships within the genus led to the conclusion that all species should be included in a single genus.     

The morphology,taxonomy and evolution ofRhodocoma (Restionaceae)

The vegetative and reproductive morphology, culm and rhizome anatomy and seed surface micromorphology ofRhodocoma are described. It is shown that this variation is best contained by recognizing three new species in the genus. These new taxa are described, and the phylogeny of the genus is investigated by cladistic analysis. The environmental parameters and distributions of the species are related to the cladogram. This suggests that the species are at present ecologically separated, and indicates that the speciation may have been sympatric. This is the first support for the hypothesis that sympatric speciation may have been important in the speciose Cape flora.     

Cyclic (1 → 2)-β-d-glucans excreted by the glucuronan-producing strain Rhizobium meffloti M5N1CS CS (NCIM B 40472) and by the succinoglycan-producing strain Rhizobium meliloti M5N1

During fermentation, the mutant strain Rhizobium mefliloti M5N1 CS, which induces nodule formation on alfalfa roots, produces a partially acetylated (1 → 4)-β-d-glucuronan. In addition to this exopolysaccharide of high molecular weight, the mutant strain produces oligoglucoronates and cyclic (1 → 2)-β-d-glucans with degrees of polymerization from 17 to 30. Under the conditions applied, magnesium has no effect on cyclic glucan production by the mutant strain, but the succinoglycan production by the wild-type strain Rhizobium meliloti M5N1 increases.     

Pollen morphology and taxonomy of Atraphaxis (Polygoneae,Polygonaceae)

Pollen grains of 32 species of Atraphaxis L. including six species previously attributed to Polygonum L. s.str. were investigated with LM (acetolysed pollen) and SEM (dry pollen). Pollen grains of all studied species are spheroidal to oblong-spheroidal, mostly tricolporate, rarely 4-6-loxocolporate, ellipsoidal in equatorial view, rounded-trilobed or trilobed in polar view, with striate or striato-perforate, reticulato-foveolate, or reticulato-perforate sporoderm ornamentation. Exine sculpture is the most variable feature, differing in width, distinctness, and spacing of the striae, which are divided by grooves with small pits or perforations in rows. The most distinct variants of sporoderm ornamentation are connected by a full range of transitions. Striato-perforate ornamentation is common in species with the perianth typical for Atraphaxis, whereas reticulato-foveolate or reticulato-perforate sporoderm ornamentation was found in species with the perianth of Polygonum-type.     

Liquid chromatographic determination of urinary 2-thiothiazolidine-4-carboxylic acid, a biomarker of carbon disulphide exposure

An effective gradient high-performance liquid chromatographic method for baseline separation of urinary 2-thiothiazolidine-4-carboxylic acid (TTCA), with photodiode array detection at 271 nm was described. o-Methylhippuric acid was used as an internal standard (I.S.). A 1-ml urine sample was saturated with 300 mg of sodium sulphate, acidified with 100 μl of 6 M hydrochloric acid, extracted twice with 2 ml of diethyl ether, and after evaporation, the residue was taken up in 1 ml of 0.1% (v/v) phosphoric acid. The two mobile phases used for gradient elution were: (A) 10 mM ammonium dihydrogenphosphate (pH 3.5) and (B) same concentration of buffer but containing 20% (v/v) of methanol (pH 4.8). The flow-rate was set at 1.0 ml/min. TTCA and I.S. were detected at 2.2 and 9.1 min, respectively. The method was validated with urine samples collected from normal subjects and workers occupationally exposed to carbon disulphide. The present method enables the detection of urinary TTCA at a concentration of 0.025 mg/l. Analytical recovery and reproducibility generally exceeded 90%. The proposed method is considered more sensitive, specific and reliable than other existing methods.     

Isolation and identification of sodium 2-propenyl thiosulfate from boiled garlic (Allium sativum) that oxidizes canine erythrocytes

Sodium 2-propenyl thiosulfate was identified in boiled garlic (Allium sativum). When canine erythrocytes were incubated with sodium 2-propenyl thiosulfate, the methemoglobin concentration and Heinz body percentage in erythrocytes were both increased, indicating that the compound induced oxidative damage in canine erythrocytes. It seems that this compound is one of the causative agents of garlic-induced hemolysis in dogs.     

Ipomoea littoralis (Convolvulaceae)—taxonomy,distribution, and ethnobotany

Ipomoea littoralis (Convolvulaceae), a member of Ipomoea section Batatas, is the only species of the section native and still endemic to the Old World. In spite of confusion in the literature, the correct name for the species is I. littoralis. Plants with which I. littoralis has been confused are endemic to Australia and are properly called I. gracilis. These two names apply to species belonging to different sections of Ipomoea. Ipomoea littoralis probably shares a common ancestor with I. ramosissima of the neotropics. Data from a variety of sources, including common association with people and the many vernacular names for the plants, indicate that they are not only wild but are also encouraged and even cultivated.     

Comparative physiology,biochemistry, and the taxonomy ofChlorella (Chlorophyceae)

According to biochemical and physiological characters, 77 strains ofChlorella were assigned to 12 taxa. The characters used are presence or absence of hydrogenase, formation of secondary carotenoids under nitrogen-deficient conditions, liquefaction of gelatin, products of glucose fermentation, ability to reduce nitrate, thiamine requirement, acid tolerance, salt tolerance, thermophily, and base composition of DNA (GC content). On the other hand, certain nutritional characters, i. e., utilization of organic carbon and nitrogen compounds, were found to be more or less strain-specific, highly variable, and therefore unsuitable for taxonomy.Presented at the symposium Speciation and the Species Concept during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

The taxonomy of Sarcocystis (Protozoa, Apicomplexa) species

The taxonomy of the heteroxenous apicomplexan protozoan genus Sarcocystis was reviewed, and a list of 122 species with their synonyms and hosts given. Both definitive and intermediate hosts are known for only 56 species. The fine structure of the sarcocyst wall may change with age and is not considered necessarily satisfactory for separating species. Specificity for the intermediate host is not narrow for all species. Earlier work on transmission of the parasite from one intermediate host to another should be repeated in the light of present knowledge of the life cycle of species of Sarcocystis.     

An appraisal of Ulva (Ulvophyceae,Chlorophyta) taxonomy

Journal of Applied Phycology - The green seaweed Ulva is important from ecological and economic perspectives, but the identification of species is often problematic. Here we assessed and discussed...     

Functional diversities of two activity components of circadian rhythm in genetical splitting mice (CS strain)

CS mice, an inbred strain, showed two distinctive characteristics in the circadian rhythm of locomotor activity: (1) large variation in the freerunning period, and (2) spontaneous rhythm splitting under continuous darkness. In the splitting rhythm there was a positive correlation between the freerunning period of the evening component and the activity time of the morning component. The phase-shifting effect of a 15-min light pulse was examined on the two activity components of the splitting rhythm. There were significant differences in the amount of light-induced phase response between the two components. A light pulse during the late subjective night induced a phase advance shift only in the morning component, while a light pulse during the early subjective night induced a phase delay shift only in the evening component. These results indicate functional diversities of the two activity components in the circadian locomotor rhythm of CS mice, and suggest that the circadian system in CS mice consists of two mutually coupled oscillators which have different circadian periods and different responsiveness to light. The CS mouse is a useful model to explore a genetic background of oscillator coupling in the circadian system of nocturnal rodents. Accepted: 19 November 1998