Changes of algal biomass as carbon, cell number and volume, in bottles suspended in Lake Constance

Changes of algal biomass, as carbon, cell numbers and volumewere determined for phytoplankton of Lake Constance suspendedin situ in 2 l glass bottles. Phytoplankton placed at the 6%surface penetrating light level (photosynthetically availableradiation) were close to the compensation depth for growth estimatedas total particulate carbon and total cell volumes. Cell countsof individual alga] species however, showed appreciable growthof diatoms offset by the decline of flagellates. Bottles suspendedat two shallower depths in a separate experiment showed somegrowth of all species and indicated a vertical niche separationof growth of Rhodomonas minuta Skuja and R. lens Dascher andRuttner in accordance with their vertical distribution. ^*This paper is the result of a study made at the Group for AquaticPrimary Productivity (GAP) First International Workshop heldat the Limnological Institute, University of Konstanz, in April1982.     

Reduction of sensory cells in antennal sensilla correlated with changes in feeding behavior in the beetle Loricera pilicornis (Insecta,Coleoptera, Carabidae)

Summary The structure of the setae on the proximal antennal segments of the beetle Loricera pilicornis is described using electron microscopical methods. These setae are part of a prey-capturing apparatus and are inserted within flexible sockets. They have no central lumen.Four or five sensory cells are connected to each seta. One cell is characterized as a mechanoreceptor due to the presence of a tubular body and the location of its dendritic outer segment. The other sensory cells are of two types. One type shows the usual features of sensillar receptors except that the dendritic outer segments end beneath the seta within the cuticular sheath. In the other type all parts of the cell, including the perikaryon, appear undersized, and no axon was found. In a single case a sixth cell was found which lacks any process, although, due to its location, it belongs to the sensory cell group.The enveloping cells also deviate from the usual pattern. Trichogen and tormogen cells have no membrane folds nor microvilli. From the membrane of the thecogen cell, where it borders on the inner receptor lymph cavity, invaginations have developed which form voluminous membrane whorls. Portasomes are found on these membranes.On the basis of the structural features we hypothesize that the setae represent sensilla undergoing stepwise reduction, losing primordial gustatory units whilst the prey-capturing mechanism is optimized.Dedicated to Professor Dr. Dietrich Schneider on occasion of his 65th birthday     

Genetic studies of the lac repressor. IX. Generation of altered proteins by the suppression of nonsence mutations.

We have generated more than 300 altered lac repressor proteins carrying known amino acid replacements, by employing nonsense mutations at 90 positions in the lacI gene together with eight different nonsense suppressors. This allows the substitution of lysine, serine, tyrosine, leucine and glutamine at virtually all of the respective positions in the repressor, and tryptophan at ten positions in the repressor. Since most of the nonsense sites have been correlated with specific codons in the lacI messenger RNA, in almost all cases the position of the substituted residue is known. This process results in the creation of a large number of mutant phenotypes. We have analyzed the effects of each substitution in vivo, and in several cases studied partially purified repressors in vitro. The properties of the altered proteins have been compared with the position and nature of each exchanged residue. We discuss the implications of these findings with regard to repressor structure in particular, and to protein structure in general. Further applications of the suppression method are also considered.     

Development of a system useful for studying the formation of unstable alleles of IS2

Summary IS2-induced deletions of the gal control region were isolated in a plasmid carrying gal OP-308 :: IS2-7. This contains a 54 basepair long, unstable mini insertion within IS2, thus allowing constitutive expression of the gal structural genes. Deletion PPI is 11.9 kilobasepairs (kb) long and is Gal⁺ because it has retained the mini insertion. In PP4 7.2 kb DNA material including markers gal OP, chlD and pgl are deleted. PP4 has lost the mini insertion and is therefore Gal negative. DNA sequencing of the newly formed junction in PP4 reveals that the deletion terminates precisely at nucleotide 1 of IS2 and that no DNA sequence homology is involved in this IS2-mediated deletion formation. PPI segregates Gal^- clones due to the loss of the mini insertion. One such segregant PPIS and PP4 both give only constitutive Gal⁺ revertants, which consist of the previously known mini insertions and also a new class of supermini inserts within IS2 of about 10 to 20 basepairs long. Therefore, PPIS and PP4 can be used to study various parameters involved in the formation of mini insertions.     

Characteristics of single chemoreceptive units sensitive to amino acids and related substances in the crayfish leg

Summary Impulses in single afferent fibres from amino acid receptors were recorded extracellularly. Doseresponse relations were determined for different superfused amino acids; the relations all had a slope of 1, a common saturation level, and the action of different amino acids was characterized by a specific half saturation concentration,K _M. The most effective amino acids were always L-serine, L-alanine and L-histidine, having aK _M of 10^–5, 2·10^–5 and 1.5·10^–4 mol/l, respectively. The sequence of effective amino acids was the same for all units tested. Structural requirements for optimal stimulatory action of the amino acid molecules were concluded.Abbreviation vH van Harreveld solution This work was supported by the Deutsche ForschungsgemeinschaftWe gratefully acknowledge assistance in electronics from Mr. W. Zeitz, and in mechanics from Mr. D. Beyer and Mr. L. Müller. Technical help was provided by Mrs. E. Köster, secretarial help by Mrs. L. Bauer.     

Properties of auxin binding sites in different subcellular fractions from maize coleoptiles

In-vitro binding of labeled auxins to sedimentable particles was tested in subcellular fractions from homogenates of maize (Zea mays L.) coleoptiles. The material was fractionated by differential centrifugation or on sucrose density gradients. It was confirmed that the major saturable binding activity (site I) for 1-naphthyl[1-¹⁴C]acetic acid is associated with vesicles derived from the endoplasmatic reticulum. A second type of specific auxin binding (site II) could be distinguished by several criteria, e.g. by the low affinity towards phenylacetic acid. The particles carrying site II could be clearly separated from markers of the endoplasmatic reticulum, the plasmalemma, the mitochondria and the nuclei, while their density as well as sedimentation velocity correlated with particle-bound acid phosphatase, indicating a localization at the tonoplast. In contrast to site I, binding at site II was hardly affected by a supernatant factor and by sulfhydryl groups. However, the specificity pattern of site II towards auxins and auxin analogs was very similar to that of site I tested in the presence of supernatant factor. The existence of a third auxin receptor localized in plasma membrane-rich gradient fractions was indicated by a preferential in-vitro binding of 2,4-dichlorophenoxyacetic acid.Abbreviations 1-NAA 1-naphthyl acetic acid - 2-NAA 2-naphthyl acetic acid - IAA 3-indolyl acetic acid - PAA phenyl acetic acid - 2,4-D 2,4-D-dichlorophenoxy acetic acid - D-2,4-DP dichlorophenoxy isopropionic acid - NPA 1-N-naphthyl phthalamic acid - ER endoplasmatic reticulum - SF supernatant factor     

Die Belichtungsreaktionen sessiler Crustaceen(Balanus balanus) als Alternative zu den Schutzreaktionen bodenbewohnender mariner Wirbelloser

Shadow responses, including reactions to both increase (on) and decrease (off) in light intensity have been hitherto described in the adults of various bottom-dwelling marine invertebrates. These reactions as expressed by decrease in activity are assumed to be protective (withdrawal responses, kinetic rigidity after v. Buddenbrock, 1952). By contrast, the free-swimming larvae of these species normally show increase in activity to both increase and decrease in light intensity as expressed by negative or positive photoresponses. In the sessile barnacleBalanus balanus L. reactions to increase in light intensity are demonstrated which, contrary to the withdrawal responses or kinetic rigidity, result in an increase of cirral activity. The shadow responses of the barnacles (off responses) are described as withdrawal responses. The light responses are expressed by two different modes of behaviour: (a) If an active barnacle is stimulated by increase in light intensity, the frequency of cirral activity increases; (b) if an inactive barnacle is stimulated by increase in light intensity, the cirral activity arises a short time later. The light responses observed are interpreted as a metamorphosis of larval swimming activity.

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Gefördert von der Deutschen Forschungsgemeinschaft     

Evolutionary conservation of a microbody targeting signal that targets proteins to peroxisomes, glyoxysomes, and glycosomes.

Peroxisomes, glyoxysomes, glycosomes, and hydrogenosomes have each been classified as microbodies, i.e., subcellular organelles with an electron-dense matrix that is bound by a single membrane. We investigated whether these organelles might share a common evolutionary origin by asking if targeting signals used for translocation of proteins into these microbodies are related. A peroxisomal targeting signal (PTS) consisting of the COOH-terminal tripeptide serine-lysine-leucine-COOH has been identified in a number of peroxisomal proteins (Gould, S.J., G.-A. Keller, N. Hosken, J. Wilkinson, and S. Subramani. 1989. J. Cell Biol. 108:1657-1664). Antibodies raised to a peptide ending in this sequence (SKL-COOH) recognize a number of peroxisomal proteins. Immunocryoelectron microscopy experiments using this anti-SKL antibody revealed the presence of proteins containing the PTS within glyoxysomes of cells from Pichia pastoris, germinating castor bean seeds, and Neurospora crassa, as well as within the glycosomes of Trypanosoma brucei. Western blot analysis of purified organelle fractions revealed the presence of many proteins containing this PTS in both glyoxysomes and glycosomes. These results indicate that at least one of the signals, and therefore the mechanism, for protein translocation into peroxisomes, glyoxysomes, and glycosomes has been conserved, lending support to a common evolutionary origin for these microbodies. Hydrogenosomes, the fourth type of microbody, did not contain proteins that cross-reacted with the anti-PTS antibody, suggesting that this organelle is unrelated to microbodies.     

G-proteins in etiolated Avena seedlings. Possible phytochrome regulation

The molecular mechanism of light signal transduction in plants mediated by the photosensor phytochrome is not well understood. The possibility that phytochrome initiates the signal transduction chain by modulating a G-protein-like receptor is examined in the present work. Etiolated Avena seedlings contain G-proteins as examined in terms of the binding of GTP as well as by cross-reaction with mammalian G-protein antibodies. The binding of GTP was regulated in vivo by red/far-red light. The possible involvement of G-proteins in the phytochrome-mediated signal transduction in etiolated Avena seedlings has been implicated from the study of the light regulated expression of the Cab and phy genes.     

Seasonal dynamics of moss-dwelling chironomid communities

Chironomid communities of mosses in a small upland stream in central Germany were highly dynamic across the year with respect to their abundance, biomass and dominant taxa. During 1988 semi-submersed mosses near a main spring and those occurring some 700 m downstream were compared with permanently submersed mosses in immediate vicinity of the downstream site. All the chironomids sampled were conspicuously small, with nearly 98% being less than 5 mm in length. A total of 65 chironomid species from 26 genera were found, with a higher diversity occurring near the source and a change in dominant taxa along the upper stream section. The mean abundance in permanently submersed mosses (250 larvae/10 cm², n = 125) was about five times higher than in semi-submersed mosses. The maximum value of 830 larvae/10 cm² (n = 1) is the highest chironomid density ever reported, which is explained by the sampling method used. The mean standing crop was also highest in permanently submersed mosses (1.5 mg AFDW/10 cm² (n = 125)), even though the highest individual value was recorded in semi-submersed mosses near the spring (10.4 mg AFDW/10 cm²). The evidence suggested that the dominance of chironomid taxa depended mainly on the location of the moss along the stream, whereas abundance and biomass were determined mainly by constancy in the ambient discharge as well as the factors influenced by this (e.g. temperature, detritus deposition). A trend was seen towards a seasonal succession among the chironomid taxa colonizing lotic mosses.