A NEW BANGIOPHYCIDEAN ALGA FROM ALABAMA1

A new species of red algae, Boldia angustata sp. nov., was discovered near Tuscaloosa, Alabama, during the spring of 1968. It differs significantly from the only previously described species, Boldia erythrosiphon Herndon, in length and width of young and mature thalli, cell size, shape of nuclei in first-order cells, shape of intercalary filaments, morphology of filaments derived from monospores, ontogenetic development of erect plants, morphology of the basal system, and regularity of first-order cells.     

ISOLATION OF A GOLGI APPARATUS-RICH FRACTION FROM RAT LIVER : II. Enzymatic Characterization and Comparison with Other Cell Fractions

Enzymatic activities associated with Golgi apparatus-, endoplasmic reticulum-, plasma membrane-, mitochondria-, and microbody-rich cell fractions isolated from rat liver were determined and used as a basis for estimating fraction purity. Succinic dehydrogenase and cytochrome oxidase (mitochondria) activities were low in the Golgi apparatus-rich fraction. On the basis of glucose-6-phosphatase (endoplasmic reticulum) and 5'-nucleotidase (plasma membrane) activities, the Golgi apparatus-rich fraction obtained directly from sucrose gradients was estimated to contain no more than 10% endoplasmic reticulum- and 11% plasma membrane-derived material. Total protein contribution of endoplasmic reticulum, mitochondria, plasma membrane, microbodies (uric acid oxidase), and lysosomes (acid phosphatase) to the Golgi apparatus-rich fraction was estimated to be no more than 20–30% and decreased to less than 10% with further washing. The results show that purified Golgi apparatus fractions isolated routinely may exceed 80% Golgi apparatus-derived material. Nucleoside di- and triphosphatase activities were enriched 2–3-fold in the Golgi apparatus fraction relative to the total homogenate, and of a total of more than 25 enzyme-substrate combinations reported, only thiamine pyrophosphatase showed a significantly greater enrichment.     

The construction of lambda transducing phages containing deletions defining regulatory elements of the lac and trp operons in E. coli

Summary Two sets of plaque-forming transducing phages have been isolated which carry parts of the tryptophan (trp) and lactose (lac) operons. The ptrp-lac set of phages carry the trp and lac operons in the same orientation connected by deletions which enter the lac regulatory region from the i side. These deletions start at various sites in or near the trp operon and end either late in the lac i gene, within the promoter, between the promoter and the operator, within the operator, between the operator and the z gene, or very early in the z gene. Starting with one particular trp-lac fusion strain, a series of transducing phages were isolated which contain varying portions of the trp operon extending from the trp A gene towards the trp operator. The other set of phages, which are designated ptrp/lac, carry trp and lac in opposing orientations. These ptrp/lac phages contain deletions which remove all of the lac structural genes and end between the operator and the z gene.A preliminary report of a portion of this work was presented at the Thirteenth International Congress of Genetics, Berkeley, 1973.     

Occurrence of Branched-Chain Hydroxy Fatty Acids in Pseudomonas maltophilia

Three branched-chain hydroxy acids not previously reported in other bacteria were found in extracts from saponified whole cells of Pseudomonas maltophilia. On the basis of evidence from mass spectrometry, infrared spectroscopy, and gas chromatographic procedures, they were identified as 2-hydroxy-9-methyldecanoic acid, 3-hydroxy-9-methyldecanoic acid, and 3-hydroxy-11-methyldodecanoic acid. These acids appeared to be tightly bound to other cellular components since they were not extracted from lyophilized cells with a chloroform-methanol (3:1) mixture.     

Use of Gas Chromatography for Determining Catabolic Products of Arginine by Bacteria

A rapid and sensitive procedure for determining catabolic products of arginine metabolism by bacteria was developed. The method consists of inoculating a solution of L-arginine with a heavy cell suspension of the test organism. After a 2-hr incubation period, dissimilation products (citrulline, ornithine, agmatine, putrescine) are converted to volatile derivatives and analyzed by gas-liquid chromatography. Compared with conventional microbiological tests, the new procedure is rapid and can be used for sensitive quantitative measurements of specific metabolites from arginine.     

Comparison of Methods for Tuberculosis Bacteriology

To improve efficiency of isolation of tubercle bacilli from clinical specimens, the following recommendations are presented. (i) Employ multiple specimens consisting of a combination of morning sputums for the early detection of positives, along with 24-hr sputum pools for the greatest total yield of positives. (ii) When timing is rigorously controlled, Zephiran-trisodium phosphate and sodium hydroxide-acetylcysteine are comparable, but if timing cannot rigidly be controlled, employ the Zephiran-trisodium phosphate digestion procedure to allow the greatest freedom in exposure time with the lowest kill rate to tubercle bacilli. (iii) Employ both an agar medium incubated in 5% CO₂, for the early detection of positives as well as positives in the presence of contaminants, and an egg medium, preferably with CO₂, to increase the yield of positives.     

A test of homology between the B chromosome of maize and abnormal chromosome 10, involving the control of nondisjunction in B's

Summary Nondisjunction of B and B-translocation chromosomes occurs regularly in maize at the second pollen mitosis (Roman, 1947; Blackwood, 1956). The mechanism of nondisjunction was studied using the A-B interchange, TB-9b. The B⁹ chromosome of the interchange undergoes nondisjunction at the second pollen mitosis, while the 9^B chromosome does not (Roman, 1947). It was shown that the 9^B chromosome must be present in a plant for nondisjunction of the B⁹ to occur. This is consistent with the reports of Roman on TB-4a (1949) and Longley on TB-10a (1956). It was also demonstrated that the influence of the 9^B chromosome is limited to pollen grains containing it, and does not extend to all the pollen of a plant.A test of homology between the B chromosome and abnormal chromosome 10 was also made. The ability of abnormal 10 to substitute for the 9^B chromosome and induce nondisjunction of the B⁹ was tested. Nondisjunction did not occur at a detectable rate in the presence of abnormal 10, and the results failed to support Ting's proposal (1958) concerning the origin of abnormal 10.     

Assessing the bioaccumulation of contaminants from sediments by fish and other aquatic organisms

Contaminated sediments that are not acutely toxic to aquatic organisms but contain bioaccumulable toxic substances present a common, yet poorly understood problem for regulatory decision makers. In order to recommend options to minimize bioaccumulation of these toxic substances, decision-makers need estimates of 1. which substances are available for accumulation by aquatic organisms; and 2. the potential impacts of such accumulation. The most direct and meaningful approach to estimating bioavailability is measurement of contaminant uptake by aquatic organisms exposed to the sediments of concern. Reasonably reliable methodologies exist for performing such exposures in the laboratory and in situ using marine or freshwater organisms. Such methods can demonstrate short-term potential for bioaccumulation of toxics from the sediments, but not necessarily the biological significance or long-term impact of any accumulated residues in the organisms and transfer of those residues through the food chain. Since most contaminated sediments contain a mixture of toxic substances, determination of the biological significance of their accumulation is not likely in the near future. Thus, the direct measurement of significant bioaccumulation of toxic substances from the sediments remains the most immediately useful index in a decision-making process.Contribution Number 631 of the National Fisheries Center-Great Lakes     

The effect of an intermittent water-table gradient on soil and xylem nitrate in cotton

Summary Cotton (Gossypium hirsutum cv Deltapine 61) was grown in a sloping plot of soil in the field to examine the effect of a gradient of water-table depth on soil nitrate availability and plant uptake during two periods of the growing season. Before the water-table was imposed NO₃ was less concentrated at the lower end of the sloping plot. This was attributed to slow denitrification at microsites within the soil at the lower end which was wetter than further up the plot. At flooding NO₃ disappeared only slowly due to a carbon substrate limitation to denitrification in the soil. This loss occurred primarily in areas where the water-table was high and oxygen concentration in the soil solution was low. Plant NO₃ uptake, assessed by measuring the concentration in the xylem, parallelled the distribution of NO₃ in the soil solution. Under high water-tables xylem NO₃ levels fell but it was not possible to say whether this was due to impaired root function or to the reduced concentration of NO₃ observed in the soil solution. At intermediate water-table depths where soil NO₃ availability remained high xylem NO₃ concentration fell relative to the well drained control plants, suggesting that flooding had damaged the root system.Manufactured by Merck. Mention of commerical names does not imply endorsement by either CSIRO or USDA.     

Investigation of a toxic water-bloom of Microcystis aeruginosa (Cyanophyceae) in Lake Akersvatn,Norway

During the summer and fall of 1984 and 1985, the eutrophic Lake Akersvatn in south-eastern Norway, used as reserve drinking water reservoir, was found to produce heavy water-blooms of the colonial blue-green alga Microcystis aeruginosa. Samples of the water-bloom were found to be toxic using the mouse bioassay. No toxin was found free in the water as detected by HPLC and mouse bioassay. The toxic cells (minimum lethal dose 8–15 mg/kg body weight in mice) and purified toxin (minimum lethal dose 50 μg/kg body weight in mice) showed signs of poisoning in laboratory rats and mice identical to that of other hepatotoxin-producing M. aeruginosa blooms and strains reported from other parts of the world. The toxin has chemical properties similar to the cyclic heptapeptide reported for a South African M. aeruginosa toxin. The toxin from Lake Akersvatn bloom material has a molecular weight of 994. The toxic bloom of M. aeruginosa persisted from August to November in 1984 and reappeared in July of 1985. While water from Lake Akersvatn was not used for municipal water supply during this period, the presence of toxic blue-green algae in a drinking water reservoir indicates the need to develop monitoring and detection methods for toxic cells and toxin(s).