Prescribed burning reduces species richness of wood-decay fungi in the forests of northwest Arkansas

The present study, which was carried out at three localities in the Ozark Mountains of northwest Arkansas, investigated the effects of prescribed burning on wood-decomposing fungi using samples of decaying woody debris (DWD) placed in plastic incubation chambers. One of the localities had not been subjected to recent prescribed burning, whereas the other localities contained both an unburned area as well as an area recently subjected to burning. In all three localities, small pieces of decaying woody debris (DWD) were collected, placed in the incubation chambers and the latter kept moist for any extended period of time. Pieces of DWD collected in the areas subjected to burning typically displayed evidence of considerable charring. Fruiting bodies appearing in the incubation chambers were removed and identified by sequencing of ribosomal DNA region. A total of 101 specimens representing 80 different taxa were recorded in the entire investigation, but the numbers of both specimens and taxa were appreciably higher for the unburned collecting sites. As such, the data obtained indicate that prescribed burning lowers the species richness of the wood-decomposing fungi associated with DWD at a particular locality. The unique aspect of the present study was the use of incubation chambers to characterize the taxa of fungi associated with CWD.     

Assessing the potential of foamed clay as a biological aerated filter (BAF) medium

Materials used previously as biological aerated filter (BAF) media have not combined optimal biofilm supporting properties with optimal wear characteristics. Increasing its bentonite content decreased the attrition rate and friability of foamed clay. Although the altered medium exhibited less surface roughness, results from small-scale reactors confirmed that it had maintained its biological attributes. This suggests that surface roughness has a limited influence on biofilm formation.     

Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome

L1 is a glycoprotein with an apparent molecular weight of 200 kDa in the developing fetus and adult central nervous system. In the peripheral nervous system, it has a molecular weight of 230 kDa. The L1 protein appears to be encoded by a single gene that has been located on the human X chromosome by in situ hybridization. In this paper we describe restriction variation in genomic DNA Southern analysis between Mus species for the K13 cDNA probe for the L1 neural cell adhesion molecule. We have designated the locus described by this variation as cell adhesion molecule L1, CamL1. The X chromosome linkage and the relative position on the X chromosome coincident with the genes Rsvp/G6pd/Cf-8 were defined in backcross matings involving M. spretus and M. musculus.     

Proline dehydrogenase from Escherichia coli K12. Properties of the membrane-associated enzyme

The pattern of protein synthesis in hepatoma cell clones was analysed by two-dimensional separation of [35S]methionine-labelled proteins. The clones were derived from the differentiated Reuber H 35 hepatoma and showed differences in the expression of a number of liver-specific functions and the resistance to the growth-inhibitory effect of glucocorticoids. Five protein spots were observed in the extracts of the differentiated Faza 967 cells that were absent from the electrophoretogram of the dedifferentiated H 56 cells. This clone, on the other hand, displayed six spots absent from Faza 967 cells. The growth of both Faza 967 and H 56 cells was strongly inhibited by 1 microM dexamethasone. The dexamethasone-resistant clone 2, a dedifferentiated derivative of Faza 967 cells, synthesized two polypeptides that were not present in Faza 967 or H 56 cells and produced four polypeptides at a lower level than Faza 967 cells. The examination of the short-term effect of dexamethasone on protein synthesis in Faza 967 cells revealed nine induced and one repressed protein spots, which appeared to be in good agreement with earlier published data. It is concluded that dedifferentiation, although bringing about marked changes in certain liver-specific functions, such as enzyme activities or protein secretion, affects only a relatively small fraction of the genes expressed.     

Genetic and biochemical analyses of protein II

We compared the structure of P.II proteins of gonococcal strain FA1090 by N-terminal sequence analysis of purified proteins and by DNA sequencing of cloned P.II genes. Regulation of P.II gene expression does not involve major DNA rearrangements, but may involve generation of frame-shifts in unexpressed P.II genes. There are probably 8 or 9 P.II genes, each possessing a common leader sequence, in the gonococcal chromosome.