The effect of zooplankton grazing on estuarine blooms of the toxic dinoflagellate Gonyaulax tamarensis

A series of short-term ^{in situ} experiments was conducted intwo Cape Cod embayments to estimate mortality rates of the toxicdinoflagellate, Gonyaulax tamarensis, resulting from grazingby zooplankton. Rates of grazing by the whole zooplankton communityand by specific zooplankton populations were measured at variouspoints in the G. tamarensis bloom cycle. The planktonic larvaeof the spionid polychaete Polydora ligni and the tintinnid ciliateFavella sp. were important grazers in the systems studied. Gonyaulax-specificclearance rates effected by Polydora ranged from 0.02 to 0.5ml individual^–1 h^–1; for Favella the range was aboutan order to magnitude lower. Peak population densities wereclose to 900 and 400 individuals 1^–1 for P. ligni andFavella, respectively. Whether measured directly or predictedas the product of individual clearance rates and numerical abundance,rates of grazing were often higher than estimated algal divisionrates in years when blooms failed to develop. A simulation modelcorroborated the results of the field study, demonstrating thatgrazing can be a significant source of mortality during blooms,and can suppress bloom development when grazers are abundant.     

A lectin and a lectin-related protein are the two most prominent proteins in the bark of yellow wood (Cladrastis lutea).

Using a combination of cDNA cloning and protein purification it is demonstrated that bark of yellow wood (Cladrastis lutea) contains two mannose/glucose binding lectins and a lectin-related protein which is devoid of agglutination activity. One of the lectins (CLAI) is the most prominent bark protein. It is built up of four 32 kDa monomers which are post-translationally cleaved into a 15 kDa and a 17 kDa polypeptide. The second lectin (CLAII) is a minor protein, which strongly resembles CLAI except that its monomers are not cleaved into smaller polypeptides. Molecular cloning of the Cladrastis lectin family revealed also the occurrence of a lectin-related protein (CLLRP) which is the second most prominent bark protein. Although CLLRP shows sequence homology to the true lectins, it is devoid of carbohydrate binding activity. Molecular modelling of the three Cladrastis proteins has shown that their three-dimensional structure is strongly related to the three-dimensional models of other legume lectins and, in addition, revealed that the presumed carbohydrate binding site of CLLRP is disrupted by an insertion of three extra amino acids. Since it is demonstrated for the first time that a lectin and a noncarbohydrate binding lectin-related protein are the two most prominent proteins in the bark of a tree, the biological meaning of their simultaneous occurrence is discussed.     

Protease inhibitors of Manduca sexta expressed in transgenic cotton

Summary To explore the effectiveness of insect derived protease inhibitors in protecting plants against insect feeding, anti-trypsin, anti-chymotrypsin and anti-elastase protease inhibitor (PI) genes from Manduca sexta L. were expressed in transgenic cotton (Gossypium hirsutum L.). From 198 independent transformants, 35 elite lines were further analyzed. Under the control of the 35S promoter of CaMV, PI accumulated to approximately 0.1% of total protein, depending on the tissue analyzed. Using cell-flow cytometry, DNA content/ nuclei of transgenic and non-transformed cotton were identical. On cotton plants expressing PIs, fecundity of Bemisia tabaci (Genn.), the sweetpotato whitefly, was reduced compared to controls. Expression of these protease inhibitors may reduce the developmental rate of B. tabaci and other insects, and provide a strategy for cotton protection.     

Antioxidant properties of catechins and proanthocyanidins: Effect of polymerisation, galloylation and glycosylation

A range of catechins and oligomeric procyanidins was purified by high performance liquid chromatography (HPLC) from grape seed, apple skin, lentil and almond flesh. Catechins, galloylated epicatechin, glycosylated catechin, procyanidin dimers, galloylated dimers, trimer, and tetramer species were all identified, purified and quantified by HPLC, LC-MS and NMR. The antioxidant properties of these compounds were assessed using two methods: (a) inhibition of ascorbate/iron-induced peroxidation of phosphatidylcholine liposomes; (b) scavenging of the radical cation of 2,2'-azinobis(3-ethyl-benzothiazoline-6-sulphonate) (ABTS) relative to the water-soluble vitamin E analogue Trolox C (expressed as Trolox C equivalent antioxidant capacity, TEAC). Antioxidant activity in the lipid phase decreased with polymerisation in contrast with antioxidant action in the aqueous phase which increased from monomer to trimer and then decreased from trimer to tetramer. Galloylation of catechin and dimeric procyanidins decreased lipid phase and increased aqueous phase antioxidant activity. Glycosylation of catechin demonstrated decreased activity in both phases.     

Laryngeal and abdominal muscle electrical activity during periodic breathing in nonsedated lambs

Kianicka, Irenej, Véronique Diaz, Sylvain Renolleau,Emmanuel Canet, and Jean-Paul Praud. Laryngeal and abdominal muscle electrical activity during periodic breathing in nonsedated lambs. J. Appl. Physiol. 84(2):669-675, 1998.We recently reported that glottic closure waspresent throughout central apneas in awake lambs. The present studytested whether glottic closure was also observed during periodicbreathing (PB). We attempted to induce PB in 21 nonsedated lambs onreturn from hypocapnic hypoxia to room air. Airflow and thyroarytenoid(a laryngeal constrictor, n = 16),cricothyroid (a laryngeal dilator, n = 10), and abdominal (n = 9) muscleelectrical activity (EMG) were monitored continuously. PB was observedin 16 lambs, with apneic phases in 8 lambs. Thyroarytenoid muscle EMGwas observed at the nadir of PB, either throughout apnea or withprolonged expiration during the lowest respiratory efforts. Phasicinspiratory cricothyroid muscle EMG and phasic expiratory abdominal EMGdisappeared at the nadir of PB. Active glottic closure at the nadir ofPB, without abdominal muscle contraction, could be a beneficialmechanism, preserving alveolar gas stores for continuing gas exchangeduring the apneic/hypopneic phase of PB. However, consequences ofactive glottic closure on ventilatory instability, either enhancing orreducing, are unknown.

     

A 6′ gentamicin acetyltransferase gene allows effective selection of tobacco transformants using kanamycin as a substrate

6 gentamicin acetyltransferases detoxify aminoglycoside antibiotics containing a 6 amino group. We tested whether a 6 gentamicin acetyltransferase gene (6 gat) of Shigella sp. is suitable as selectable gene in plant transformation using kanamycin (Km) as a substrate. A comparative transformation experiment using Nicotiana tabacum SR1 protoplasts showed that 6 gat is as effective for selection of transformants as the commonly used neomycin phosphotransferase II (nptII). In stably transformed plants we detected moderate levels of the 6 gat mRNA. An enzymatic assay was developed with which the acetyltransferase activity of the protein is easily demonstrated.     

Effects of source of macronutrients and plant growth regulator concentrations on shoot proliferation of Cornus florida

Nodal stem segments of flowering dogwood (Cornus florida L.) were cultured on media containing seven different sources of macronutrients including full- and half-strength Murashige & Skoog (MS) macrosalts, N6, Anderson's (AND), Quoirin & Lepoivre's (LP), Nitsch & Nitsch (NIT), and Woody Plant Medium (WPM). All media contained MS micronutrients, Staba vitamins, 20 g l^-1 sucrose, and 6.5 g l^-1 Difco Bacto-agar, and were supplemented with 2.2 M 6-benzyladenine (BA) and 0.49 M indole-3-butyric acid (IBA). Following three subcultures, the best shoot proliferation was supported on media containing WPM macronutrients. To optimize the proliferation rate, shoots were cultured on WPM macronutrients supplemented with eight combinations of BA and IBA, and 3.3 M BA without IBA was determined to be the best.Abbreviations BA 6-benzyladenine - IBA indole-3-butyric acid     

Compared effectiveness of antibiotic treatments and shoot tip culture on bacterial decontamination of an in vitro propagated clone of hybrid walnut (Juglans nigra x J. regia)

Two ways were tested to obtain the definitive bacterial decontamination of a clone of hybrid walnut culturedin vitro: treatment of the plantlets with Rifampicin and other antibiotic agents, and culture establishmentvia shoot tip expiants. The former failed whereas the latter led to plantlets truly free of contaminants which could be satisfactory propagated, rooted and weaned     

Co-Expression of Cytokeratins and Vimentin in Sheep Cumulus-Oocyte Complexes. Alteration of Intermediate Filament Distribution by Acrylamide

The association between germ cells and somatic granulosa cells persists throughout the growth of the oocyte by means of foot processes of the cumulus corona cells that cross the zona pellucida. During meiotic maturation important nuclear and cytoplasmic events occur in cumulus-oocyte complex suggesting implication of cytoskeletal elements. Immunoblotting analysis of cytoskeletal proteins of the cumulus cells revealed the presence of vimentin polypeptide and of at least two cytokeratin polypeptides. Using immunofluorescence techniques on cryostat sections through frozen tissue, we provided evidence for the presence of cytokeratins of the simple epithelial type in addition to vimentin in sheep cumulus cells. These two types of intermediate filaments were localized throughout the cytoplasm and especially in the foot processes which cross the zona pellucida. The contact area between the two cell types was also labelled with the antibodies. Acrylamide treatment of cumulus-oocyte complexes involved a drastic disorganization of the intermediate filament network and triggered the isolation of the oocyte from its cumulus cells. This isolation resulted in resumption of meiosis. From these results it appears that intermediate filaments could participate in the process of gap junction loss and indirectly in the control of meiosis resumption.