Can chaoborid larvae control their zooplanktonic prey populations in a neotropical lake?

Although it is well known that predatory Chaoborus Lichtenstein 1800 larvae have a strong negative impact on zooplankton populations in many Holarctic lakes, this top‐down control is still not entirely clear in the Neotropics. In Lake Carioca, a Brazilian monomictic lake, chaoborids became one of the main zooplankton predators after the depletion of planktivorous fish by non‐native piscivorous fish. The aim of this research was to test the hypothesis that Chaoborus spp. larvae control the density of their prey populations. Enclosures simulated conditions with higher (Pr+) and lower (Pr?) predatory Chaoborus spp. larva densities over 30 days in two periods (stratification and mixing). Our results indicated that the dominant copepod species was affected only in the stratification period when its population was smaller. In this circumstance, predated individuals were probably not replaced in the same proportion by reproductive output of the smaller population. Rotifers were not sensitive to changes in chaoborids densities in both periods. The lack of a strong top‐down effect recorded by our mesocosm experiments emphasises the importance of continuing to investigate the ecological roles played by this invertebrate predator in aquatic food webs and if its ability to regulate the zooplankton in most Holarctic lakes can (or cannot) be widely generalised to Neotropical communities. Such a result also suggests that alternative research approaches, besides in‐situ experiments, may be necessary to better clarify this topic. Specifically for cladocerans, parallel paleolimnological analyses in Lake Carioca have supported the idea of a possible negative impact of Chaoborus larvae on bosminids after the introduction of non‐native piscivorous fishes. Abstract in Portuguese is available with online material.     

Purification and characterization of glutamine synthetase from the unicellular cynabacterium Anacystis nidulans

Glutamine synthetase from the unicellular cynabacterium Anacystis nidulans was found associated with the membrane fraction of cell-free extracts. The enzyme could be solubilized by treatment of the cell membranes with the detergent alkyltrimethylammoniun and was purified to electrophoretical homogeneity by using affinity chromatography on 2′,5′-ADP-Sepharose. The molecular weight of the native enzyme was approx. 575000 but only a single protein band of 47 kDa was detected after sodium dodecyl sulphate gel electrophoresis, which implies a native enzyme complex with twelve identically sized subunits. Values for apparent Michaelis constant of the purified enzyme for ammonium, glutamate and ATP were 20, 5000 and 700 μM, respectively. Alanine behaved as an inhibitor of both activities (transferase and biosynthetic) of glutamine synthetase, whereas aspartate, leucine and lysine inhibited the biosynthetic activity of the enzyme, and glycine and serine only inhibited the transferase activity. Glutamate analogs, such as hydroxylysine, methionine sulfone, methionine sulfoximine and phosphinothricin, which inhibited ammonium uptake in vivo, behaved as potent inhibitors of glutamine synthetase in vitro. A. nidulans glutamine synthetase was inhibited by p-hydroxymercuribenzoate, the effect being reversed by treatment with dithioerythritol, dithiothreitol or mercaptoethanol.     

Mutational analysis of Asp51 of Anabaena azollae glutamine synthetase. D51E mutation confers resistance to the active site inhibitors L-methionine-DL-sulfoximine and phosphinothricin.

The role of Asp51 in the catalytic activity of glutamine synthetase from the cyanobacterium Anabaena azollae has been analyzed. Five mutant enzymes, D51S, D51A, D51E, D51N and D51R, were constructed by site-directed mutagenesis and characterized. Asp51 appears to participate in the binding of ammonium ion, as affinity for this substrate was affected in all cases, although it varied according to the charge and/or size of the amino-acid residue, decreasing in the order Glu > Asn > Ser > Ala. The replacement of Asp51 by Glu (D51E) conferred besides a high resistance to the herbicides L-methionine-DL-sulfoximine and phosphinothricin, as a result of a decreased phosphorylation ability.