Some like it hot: the physiological ecology of C4 plant evolution

Oecologia - The evolution of C4 photosynthesis requires an intermediate phase where photorespiratory glycine produced in the mesophyll cells must flow to the vascular sheath cells for metabolism by...     

Monitoring the positioning of short polycationic peptides in model lipid bilayers by combining hydrogen/deuterium exchange and electrospray ionization mass spectrometry

Electrospray ionization mass spectrometry (ESI-MS) was used to analyze the hydrogen/deuterium exchange properties of the mastoparan peptide Apoica-MP during interactions with lipid vesicle membranes. Synthetic peptide was incorporated into large unilamellar vesicles (LUVs) of L-alpha-phosphatidylcholine (PC), resulting in proteoliposomes which were then diluted with D2O. After quenching deuteration by the addition of formic acid the H/D exchange was directly analyzed by ESI-MS. This strategy was used to investigate the architecture of the peptide in the membranes of PC LUVs. The deuterated peptide ions were analyzed under collision-induced dissociation (CID) mass spectrometry, which permitted the location of deuterons at the amide sites along the peptide backbone. Intramolecular hydrogen scrambling was investigated both in the free peptide and in its proteoliposome form. Some scrambling was observed for the free peptide; however, almost no scrambling occurred in the amide hydrogens of the peptide backbone embedded in the membrane. The CID spectra suggest that the N-terminal moiety of the peptide lies on the polar side of the lipid membrane, while the C-terminal region is embedded in the membrane. The protocol described here may be reliably applied to investigate the interaction of mastoparans with bilayer lipid systems.     

Isoprene emission from aspen leaves : influence of environment and relation to photosynthesis and photorespiration

Isoprene emission rates from quaking aspen (Populus tremuloides Michx.) leaves were measured simultaneously with photosynthesis rate, stomatal conductance, and intercellular CO₂ partial pressure. Isoprene emission required the presence of CO₂ or O₂, but not both. The light response of isoprene emission rate paralleled that of photosynthesis. Isoprene emission was inhibited by decreasing ambient O₂ from 21% to 2%, only when there was oxygen insensitive photosynthesis. Mannose (10 millimolar) fed through cut stems resulted in strong inhibition of isoprene emission rate and is interpreted as evidence that isoprene biosynthesis requires either the export of triose phosphates from the chloroplast, or the continued synthesis of ATP. Light response experiments suggest that photosynthetically generated reductant or ATP is required for isoprene biosynthesis. Isoprene biosynthesis and emission are not directly linked to glycolate production through photorespiration, contrary to previous reports. Isoprene emission rate was inhibited by above-ambient CO₂ partial pressures (640 microbar outside and 425 microbar inside the leaf). The inhibition was not due to stomatal closure. This was established by varying ambient humidity at normal and elevated CO₂ partial pressures to measure isoprene emission rates over a range of stomatal conductances. Isoprene emission rates were inhibited at elevated CO₂ despite no change in stomatal conductance. Addition of abscisic acid to the transpiration stream dramatically inhibited stomatal conductance and photosynthesis rate, with a slight increase in isoprene emission rate. Thus, isoprene emission is independent of stomatal conductance, and may occur through the cuticle. Temperature had an influence on isoprene emission rate, with the Q₁₀ being 1.8 to 2.4 between 35 and 45°C. At these high temperatures the amount of carbon lost through isoprene emission was between 2.5 and 8% of that assimilated through photosynthesis. This represents a significant carbon cost that should be taken into account in determining midsummer carbon budgets for plants that are isoprene emitters.     

Deformations and end effects in isolated blood vessel testing

Blood vessels are commonly studied in isolation to define their mechanical and biological properties under controlled conditions. While sections of the wall are sometimes tested, vessels are most often attached to needles and examined in their natural cylindrical configuration where combinations of internal pressure and axial force can be applied to mimic in vivo conditions. Attachments to needles, however, constrain natural vessel response, resulting in a complex state of deformation that is not easily determined. As a result, measurements are usually limited to the midsection of a specimen where end effects do not extend and the deformation is homogeneous. To our knowledge, however, the boundaries of this uninfluenced midsection region have not been explored. The objective of this study was to define the extent of these end effects as a function of vessel geometry and material properties, loading conditions, and needle diameter. A computational fiber framework was used to model the response of a nonlinear anisotropic cylindrical tube, constrained radially at its ends, under conditions of axial extension and internal pressure. Individual fiber constitutive response was defined using a Fung-type strain energy function. While quantitative results depend on specific parameter values, simulations demonstrate that axial stretch is always highest near the constraint and reduces to a minimum in the uninfluenced midsection region. Circumferential stretch displays the opposite behavior. As a general rule, the length of the region disturbed by a needle constraint increases with the difference between the diameter of the needle and the equilibrium diameter of the blood vessel for the imposed loading conditions. The reported findings increase the understanding of specimen deformation in isolated vessel experiments, specifically defining considerations important to identifying a midsection region appropriate for measurement.     

Ecological and evolutionary aspects of isoprene emission from plants

Isoprene (2-methyl-1,3,-butadiene), produced by many woody and a few herbaceous plant species, is the dominant volatile organic compound released from vegetation. It represents a non-trivial carbon loss to the plant (typically 0.5–2%, but much higher as temperatures exceed 30°C), and plays a major role in tropospheric chemistry of forested regions, contributing to ozone formation. This review summarizes current knowledge concerning the occurrence of isoprene production within the plant kingdom, and discusses other aspects of isoprene biology which may be of interest to the ecological community. The ability to produce significant amounts of isoprene may or may not be shared by members of the same plant family or genus, but emitting species have been found among bryophytes, ferns, conifers and Ephedra and in approximately one-third of the 122 angiosperm families examined. No phylogenetic pattern is obvious among the angiosperms, with the trait widely scattered and present (and absent) in both primitive and derived taxa, although confined largely to woody species. Isoprene is not stored within the leaf, and plays no known ecological role as, for example, an anti-herbivore or allelopathic agent. The primary short-term controls over isoprene production are light and temperature. Growth in high light stimulates isoprene production, and growth in cool conditions apparently inhibits isoprene, production of which may be induced upon transfer to warmer temperatures. The stimulation of isoprene production by high irradiance and warm temperatures suggests a possible role in ameliorating stresses associated with warm, high-light environments, a role consistent with physiological evidence indicating a role in thermal protection. Received: 1 April 1998 / Accepted: 9 November 1998     

Effect of transfer of one or two in vitro-produced embryos and post-transfer administration of gonadotropin releasing hormone on pregnancy rates of heat-stressed dairy cattle

Pregnancy rates following transfer of an in vitro-produced (IVP) embryo are often lower than those obtained following transfer of an embryo produced by superovulation. The purpose of the current pair of experiments was to examine two strategies for increasing pregnancy rates in heat stressed, dairy recipients receiving an IVP embryo. One method was to transfer two embryos into the uterine horn ipsilateral to the CL, whereas the other method involved injection of GnRH at Day 11 after the anticipated day of ovulation. In Experiment 1, 32 virgin crossbred heifers and 26 lactating crossbred cows were prepared for timed embryo transfer by being subjected to a timed ovulation protocol. Those having a palpable CL were randomly selected to receive one (n = 31 recipients) or two (n = 27 recipients) embryos on Day 7 after anticipated ovulation. At Day 64 of gestation, the pregnancy rate tended to be higher (P = 0.07) for cows than for heifers. Heifers that received one embryo tended to have a higher pregnancy rate than those that received two embryos (41% versus 20%, respectively) while there was no difference in pregnancy rate for cows that received one or two embryos (57% versus 50%, respectively). Pregnancy loss between Day 64 and 127 only occurred for cows that received two embryos (pregnancy rate at Day 127=17%). Between Day 127 and term, one animal (a cow with a single embryo) lost its pregnancy. There was no difference in pregnancy rates at Day 127 or calving rates between cows and heifers, but females that received two embryos had lower Day-127 pregnancy rates and calving rates than females that received one embryo (P < 0.03). Of the females receiving two embryos that calved, 2 of 5 gave birth to twins. For Experiment 2, 87 multiparous, late lactation, nonpregnant Holstein cows were synchronized for timed embryo transfer as in Experiment 1. Cows received a single embryo in the uterine horn ipsilateral to the ovary containing the CL and received either 100 microg GnRH or vehicle at Day 11 after anticipated ovulation (i.e. 4 days after embryo transfer). There was no difference in pregnancy rate for cows that received the GnRH or vehicle treatment (18% versus 17%, respectively). In conclusion, neither unilateral transfer of two embryos nor administration of GnRH at Day 11 after anticipated ovulation improved pregnancy rates of dairy cattle exposed to heat stress.     

Phylogeny and expression of carbonic anhydrase-related proteins

Background  

Carbonic anhydrases (CAs) are found in many organisms, in which they contribute to several important biological processes. The vertebrate α-CA family consists of 16 subfamilies, three of which (VIII, X and XI) consist of acatalytic proteins. These are named carbonic anhydrase related proteins (CARPs), and their inactivity is due to absence of one or more Zn-binding histidine residues. In this study, we analyzed and evaluated the distribution of genes encoding CARPs in different organisms using bioinformatic methods, and studied their expression in mouse tissues using immunohistochemistry and real-time quantitative PCR.