Hydrogen production by rumen holotrich protozoa: effects of oxygen and implications for metabolic control by in situ conditions

Experiments with washed suspensions of holotrich protozoa (Isotricha spp. and Dasytricha ruminantium) showed that both organisms have an efficient O2-scavenging capability (apparent Km values 2.3 and 0.3 microM, respectively). Reversible inhibition of H2 production increased almost linearly with increasing O2 up to 1.5 microM; higher levels of O2 gave irreversible inhibition. In situ determinations of H2, CH4, O2 and CO2 in ovine rumen liquor, using a membrane inlet mass spectrometer probe, indicated that O2 was present before feeding at 1-1.5 microM and decreased to undetectable levels (less than 0.25 microM) within 25 min after feeding. A transient increase in O2 concentration after feeding occurred only in defaunated animals and resulted in suppression of CH4 and CO2 production. The presence of washed holotrich protozoa decreases the O2 sensitivity of CH4 production by suspensions of a cultured methanogenic bacterium Methanosarcina barkeri. It is concluded that holotrich protozoa play a role in ruminal O2 utilization as well as in the production of fermentation end products (especially short-chain volatile fatty acids) utilized by the ruminant and H2 utilized by methanogenic bacteria. These hydrogenosome-containing protozoa thus both control patterns of fermentation by influencing O2 levels, and are themselves regulated by the low ambient O2 concentrations they experience in the rumen.     

Fungal proteinase expression in the interaction of the plant pathogen Magnaporthe poae with its host.

Infection by pathogenic fungi involves breaching the outer layer of the host by either mechanical or enzymatic means. Subtilisin-like proteinases are considered to be important in the infection process of entomopathogenic, nematophagous, and mycoparasitic fungi. Little is known regarding the expression of such proteinases by plant pathogenic fungi. Magnaporthe poae, a fungal pathogen of Kentucky bluegrass, expressed a subtilisin-like proteinase, proteinase Mp1, in the infected roots. Antibody was produced against the purified enzyme. From immunoblot analysis, expression of the proteinase in infected roots correlated with increasing severity of disease symptoms. Sequence analysis of a genomic clone indicated proteinase Mp1 was homologous to other fungal subtilisin-like proteinases. DNA gel blot analysis indicated proteinase Mp1 was encoded by a small gene family.     

The in vivo and in vitro transmission frequencies of the tw5-haplotype in mice

The recessive tw5-haplotype, a complete haplotype, is transmitted by heterozygous male mice at very high frequencies (greater than 0.90) in normal matings. The present studies were undertaken to determine the effects of delayed matings and in vitro fertilizations on this phenotypic expression. Males carrying the tw5-haplotype (+/tw5) were first tested for their frequencies of transmission of the mutant 17th chromosome in both normal and delayed matings. Spermatozoa obtained from these same males were then used to fertilize eggs in vitro. The in vivo and in vitro transmission frequencies were found to be statistically equivalent in all types of inseminations. An in vitro fertilization time course study showed that the same percentages of eggs are fertilized by tw5-bearing spermatozoa when the gametes are coincubated for either 2 or 6 h. The data lead to the conclusion that the transmission frequency of the tw5-haplotype is not affected either by the length of time elapsing between insemination and fertilization or by the environment in which fertilization occurs.     

The transmission ratio distortion of the th2-haplotype in vivo and in vitro

The th2-haplotype is transmitted at low frequencies (less than 0.30) by +/th2 males in normal matings. In the studies described here, the transmission frequency of the th2-haplotype from Rb7/th2 males was determined for normal and delayed matings and in vitro inseminations. The data show the transmission frequency from the two in vivo inseminations to be less than 0.30 and to be statistically equivalent. However, the in vitro transmission frequency (0.80) is significantly greater than either of the in vivo frequencies. The results show that the environment in which fertilization occurs affects the transmission frequency of this specific t-haplotype significantly.     

Phytochrome Control of Nyetinasty in Samanea as Modified by Oxgen, Submergence, and Chemicals

Samanea saman has rapid phytochrome-regulated nyctinasty: red light preceding darkness causes pinnules to close while far-rod light allows opening- Not only the initial angle of the pinnules, but the degree of control by phytochrome depends on the “subjective time of day” at which the tissue is exposed. Excised pairs of pinnules close rapidly when submerged in water; such closure is prevented by bubbling oxygen through the water. However, if submergence closure were due solely to low oxygen levels, then nonsubmerged pinnules in a pure nitrogen atmosphere should also close. Instead, they neither close nor respond to light, but they do respond when air is readmitted, indicating that oxygen is necessary for movement rather than for photoreception. The closure of submerged pinnules remains unexplained. Attempts to detect effects of red or far-red on oxygen uptake by pulvinus tissue were unsuccessful. The following method has been used to test the effects of various inhibitors and other substances: pinnules are excised at the first hour of the day, trimmed, submerged in a sealed chamber, given far-red light, and left in darkness while oxygen is bubbled through the medium. Concentrated test solutions are injected either initially or when the red and far-red exposures are given. Thus far, the substances tested have had little or no effect on the phytochrome response.     

EXPERIMENTAL CONTROL OF FLOWERING IN LEMNA I. GENERAL METHODS. PHOTOPERIODISM IN L. PEPUSILLA 6746

Hillman , William S. (Yale U., New Haven, Conn.) Experimental control of flowering in Lemna. I. General methods. Photoperiodism in L. perpusilla 6746. Amer. Jour. Bot. 46(6): 466–473. Illus. 1959.—Lemna perpusilla strain 6746 flowers as a typical short-day plant when grown aseptically in Hutner's medium (containing ethylenediaminetetraacetic acid, [EDTA]) at 26–28°C. A method is described for quantitatively assaying the degree of flowering in a culture. Maximal flowering takes place under photoperiods of 6–11 hr., and none under photoperiods exceeding 15 hr. The flower-promoting effects of long nights are inhibited by brief interruptions with red light, such interruptions being most effective in the middle of the dark period. A single long night will cause the subsequent production of flowering fronds, but vegetative growth in the culture is resumed after a time. Only frond primordia at a very early stage of development appear to be sensitive to induction. Quantitative flowering experiments lasting a week or less can easily be performed with this plant; it is ideally suited for studies of the effects of light, darkness, temperature, organic compounds and other factors under highly controlled conditions.     

Mutations in the Drosophila Pushover Gene Confer Increased Neuronal Excitability and Spontaneous Synaptic Vesicle Fusion

We describe the identification of a gene called pushover (push), which affects both behavior and synaptic transmission at the neuromuscular junction. Adults carrying either of two mutations in push exhibit sluggishness, uncoordination, a defective escape response, and male sterility. Larvae defective in push exhibit increased release of transmitter at the neuromuscular junction. In particular, the frequency of spontaneous transmitter release and the amount of transmitter release evoked by nerve stimulation are each increased two- to threefold in push mutants at the lowest external [Ca(2+)] tested (0.15 mM). Furthermore, these mutants are more sensitive than wild type to application of the potassium channel-blocking drug quinidine: following qunidine application, push mutants, but not wild-type, display repetitive firing of the motor axon, leading to repetitive muscle postsynaptic potentials. The push gene thus might affect both neuronal excitability and the transmitter release process. Complementation tests and recombinational mapping suggest that the push mutations are allelic to a previously identified P-element-induced mutation, which also causes behavioral abnormalities and male sterility.