A Qualitative Examination of Graduate Advising Relationships:The Advisee Perspective

Sixteen 3rd-year counseling psychology doctoral students were interviewed about their relationships with their graduate advisors. Of those students, 10 were satisfied and 6 were unsatisfied with their advising relationships. Satisfied and unsatisfied students differed on several aspects of the advising relationship, including (a) the ability to choose their advisors, (b) the frequency of meetings with their advisors, (c) the benefits and costs associated with their advising relationships, and (d) how conflict was dealt with in the advising relationship. Furthermore, all of the satisfied students reported that their advising relationships became more positive over time, whereas many of the unsatisfied students reported that their advising relationships got worse (e.g., became more distant) over time

AVAST Survey 0.4-1.0 {\mu}m Spectroscopy of Igneous Asteroids in the Inner and Middle Main Belt

We present the spectra of 60 asteroids, including 47 V-types observed during the first phase of the Adler V-Type Asteroid (AVAST) Survey. SDSS photometry was used to select candidate V-type asteroids for follow up by nature of their very blue $i-z$ color. 47 of the 61 observed candidates were positively classified as V-type asteroids, while an additional six show indications of a 0.9 $\mu$m feature consistent with V-type spectra, but not sufficient for formal classification. Four asteroids were found to be S-type, all of which had $i-z$ values very near the adopted AVAST selection criteria of $i-z \le -0.2$, including one candidate observed well outside the cut (at a mean $i-z$ of -0.11). Three A-type asteroids were also identified. Six V-type asteroids were observed beyond the 3:1 mean motion resonance with Jupiter, including the identification of two new V-type asteroids (63085 and 105041) at this distance. Six V-type asteroids were observed with low ($<5\deg$) orbital inclination, outside of the normal dynamical range of classic Vestoids, and are suggestive of a non-Vesta origin for at least some of the population.Comment: 1 table, 3 figures, To appear to Icaru

Impact histories of Vesta and Vestoids inferred from howardites, eucrites and diogenites

The parent body of the howardites, eucrites and diogenites (HEDs) is thought to be asteroid (4) Vesta [1]. However, several eucrites have now been recognized, like NWA 011 and Ibitira, with major element compositions and mineralogy like normal eucrites but with different oxygen isotope compositions and minor element concentrations suggesting they are not from the same body [2, 3]. The discoveries of abnormal eucrites and V-type asteroids that are probably not from Vesta [see 4] raise the question whether the HEDs with normal oxygen isotopes are coming from Vesta [3]. To address this issue and understand more about the evolution of Vesta in preparation for the arrival of the Dawn spacecraft, we integrate fresh insights from Ar-Ar dating and oxygen isotope analyses of HEDs, radiometric dating of differentiated meteorites, as well as dynamical and astronomical studies of Vesta, the Vesta asteroid family (i.e., the Vestoids), and other V-type asteroids

The astorb database at Lowell Observatory

The astorb database at Lowell Observatory is an actively curated catalog of all known asteroids in the Solar System. astorb has heritage dating back to the 1970s and has been publicly accessible since the 1990s. Work began in 2015 to modernize the underlying database infrastructure, operational software, and associated web applications. That effort involved the expansion of astorb to incorporate new data such as physical properties (e.g. albedo, colors, spectral types) from a variety of sources. The data in astorb are used to support a number of research tools hosted at https://asteroid.lowell.edu. Here we present a full description of the software tools, computational foundation, and data products upon which the astorb ecosystem has been built. (c) 2022 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).Peer reviewe

Escherichia coli peptide methionine sulfoxide reductase gene:regulation of expression and role in protecting against oxidative damage

This is the publisher's version, also available electronically from "http://jb.asm.org".The Escherichia coli peptide methionine sulfoxide reductase gene (msrA) encodes a single-subunit polypeptide of 212 amino acid residues (M. A. Rahman, H. Nelson, H. Weissbach, and N. Brot, J. Biol. Chem. 267:15549-15551, 1992). RNA blot analysis showed that the gene is transcribed into an mRNA of about 850 nucleotides. The promoter region was characterized, and the transcription initiation site was identified by primer extension. The synthesis of the MsrA protein increased about threefold in a growth-phase-dependent fashion. In an attempt to define the in vivo role of msrA, a chromosomal disruption was constructed. This mutant was more sensitive to oxidative stress, suggesting that oxidation of methionine in proteins plays an important role in oxidative damage

Significance of Four Methionine Sulfoxide Reductases in Staphylococcus aureus

Staphylococcus aureus is a major human pathogen and emergence of antibiotic resistance in clinical staphylococcal isolates raises concerns about our ability to control these infections. Cell wall-active antibiotics cause elevated synthesis of methionine sulfoxide reductases (Msrs: MsrA1 and MsrB) in S. aureus. MsrA and MsrB enzymes reduce S-epimers and R-epimers of methionine sulfoxide, respectively, that are generated under oxidative stress. In the S. aureus chromosome, there are three msrA genes (msrA1, msrA2 and msrA3) and one msrB gene. To understand the precise physiological roles of Msr proteins in S. aureus, mutations in msrA1, msrA2 and msrA3 and msrB genes were created by site-directed mutagenesis. These mutants were combined to create a triple msrA (msrA1, msrA2 and msrA3) and a quadruple msrAB (msrA1, msrA2, msrA3, msrB) mutant. These mutants were used to determine the roles of Msr proteins in staphylococcal growth, antibiotic resistance, adherence to human lung epithelial cells, pigment production, and survival in mice relative to the wild-type strains. MsrA1-deficient strains were sensitive to oxidative stress conditions, less pigmented and less adherent to human lung epithelial cells, and showed reduced survival in mouse tissues. In contrast, MsrB-deficient strains were resistant to oxidants and were highly pigmented. Lack of MsrA2 and MsrA3 caused no apparent growth defect in S. aureus. In complementation experiments with the triple and quadruple mutants, it was MsrA1 and not MsrB that was determined to be critical for adherence and phagocytic resistance of S. aureus. Overall, the data suggests that MsrA1 may be an important virulence factor and MsrB probably plays a balancing act to counter the effect of MsrA1 in S. aureus.This work was supported in part by a Warner/Fermaturo grant and A.T. Still University Board of Trustees Research Funds, by grant 1R15AI090680-01 from the National Institutes of Health to VKS, and grants from the Kirksville College of Osteopathic Medicine Biomedical Sciences Graduate Program to TRJ and KRB. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

Conditional Allocation of Control Rights in Venture Capital Finance

When a young entrepreneurial firm matures, it is often necessary to replace the founding entrepreneur by a professional manager. This replacement decision can be affected by the private benefits of control enjoyed by the entrepreneur which gives rise to a conflict of interest between the entrepreneur and the venture capitalist. We show that a combination of convertible securities and contingent control rights can be used to resolve this conflict efficiently. This contractual arrangement is frequently observed in venture capital finance

Hyperglycemia and redox status regulate RUNX2 DNA-binding and an angiogenic phenotype in endothelial cells

Angiogenesis is regulated by hyperglycemic conditions, which can induce cellular stress responses, reactive oxygen species (ROS), and anti-oxidant defenses that modulate intracellular signaling to prevent oxidative damage. The RUNX2 DNA-binding transcription factor is activated by a glucose-mediated intracellular pathway, plays an important role in endothelial cell (EC) function and angiogenesis, and is a target of oxidative stress. RUNX2 DNA-binding and EC differentiation in response to glucose were conserved in ECs from different tissues and inhibited by hyperglycemia, which stimulated ROS production through the aldose reductase glucose-utilization pathway. Furthermore, the redox status of cysteine and methionine residues regulated RUNX2 DNA-binding and reversal of oxidative inhibition was consistent with an endogenous Methionine sulfoxide reductase-A (MsrA) activity. Low molecular weight MsrA substrates and sulfoxide scavengers were potent inhibitors of RUNX2 DNA binding in the absence of oxidative stress, but acted as antioxidants to increase DNA binding in the presence of oxidants. MsrA was associated with RUNX2:DNA complexes, as measured by a sensitive, quantitative DNA-binding ELISA. The related RUNX2 protein family member, RUNX1, which contains an identical DNA-binding domain, was a catalytic substrate of recombinant MsrA. These findings define novel redox pathways involving aldose reductase and MsrA that regulate RUNX2 transcription factor activity and biological function in ECs. Targeting of these pathways could result in more effective strategies to alleviate the vascular dysfunction associated with diabetes or cancer