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1.
Structure ; 30(8): 1088-1097.e3, 2022 08 04.
Article in English | MEDLINE | ID: mdl-35660157

ABSTRACT

The bacterial peptidoglycan enclosing the cytoplasmic membrane is a fundamental cellular architecture. The integral membrane protein MurJ plays an essential role in flipping the cell wall building block Lipid II across the cytoplasmic membrane for peptidoglycan biosynthesis. Previously reported crystal structures of MurJ have elucidated its V-shaped inward- or outward-facing forms with an internal cavity for substrate binding. MurJ transports Lipid II using its cavity through conformational transitions between these two forms. Here, we report two crystal structures of inward-facing forms from Arsenophonus endosymbiont MurJ and an unprecedented crystal structure of Escherichia coli MurJ in a "squeezed" form, which lacks a cavity to accommodate the substrate, mainly because of the increased proximity of transmembrane helices 2 and 8. Subsequent molecular dynamics simulations supported the hypothesis that the squeezed form is an intermediate conformation. This study fills a gap in our understanding of the Lipid II flipping mechanism.


Subject(s)
Escherichia coli Proteins , Bacterial Proteins/chemistry , Escherichia coli/chemistry , Escherichia coli/genetics , Escherichia coli Proteins/chemistry , Lipids , Peptidoglycan/chemistry , Phospholipid Transfer Proteins/chemistry , Protein Conformation
2.
Theor Appl Genet ; 109(3): 523-33, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15150691

ABSTRACT

In an effort to better understand the dramatic differences in vegetative and floral morphology that differentiate species within the genus Lycopersicon, quantitative trait loci (QTL) for leaflet and perianth size and shape characters were mapped in an interspecific F2 population of tomato (Lycopersicon esculentum x L. pennellii). Thirty-six highly significant (P < or = 0.001) QTL were associated with 18 separate traits. QTL for correlated traits were generally not colocalized in the genome unless there was a clear codependence between the traits (e.g., organ length and area). Little or no overlap in QTL positioning between different organs was observed, suggesting that the genes determining the size and shape of leaflets, sepals, and petals are organ specific. Thus, while leaves are considered the developmental and evolutionary precursors to floral organs, genes acting late in development to determine certain aspects of morphology (namely shape and size) must have specialized to exert control over individual organs. Five of the leaflet-trait QTL map to analogous regions in the genome of eggplant, and therefore it appears there has been some conservation in the genes controlling leaf morphology within the Solanaceae.


Subject(s)
Chromosome Mapping , Flowers/genetics , Phenotype , Plant Leaves/genetics , Quantitative Trait Loci , Solanum lycopersicum/genetics , Crosses, Genetic , Epistasis, Genetic , Flowers/anatomy & histology , Gene Expression Regulation, Developmental/genetics , Genetic Markers/genetics , Genotype , Solanum lycopersicum/anatomy & histology , Plant Leaves/anatomy & histology
3.
Emerg Infect Dis ; 10(2): 317-9, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15030704

ABSTRACT

A global outbreak of severe acute respiratory syndrome (SARS) caused by a novel coronavirus began in March 2003. The rapid emergence of SARS and the substantial illness and death it caused have made it a critical public health issue. Because no effective treatments are available, an intensive effort is under way to identify and test promising antiviral drugs. Here, we report that recombinant human interferon-beta 1a potently inhibits SARS coronavirus replication in vitro.


Subject(s)
Antiviral Agents/pharmacology , Interferon-beta/pharmacology , Severe acute respiratory syndrome-related coronavirus/drug effects , Severe acute respiratory syndrome-related coronavirus/physiology , Virus Replication/drug effects , Animals , Chlorocebus aethiops , Cytopathogenic Effect, Viral/drug effects , Humans , In Vitro Techniques , Interferon Type I/pharmacology , Interferon beta-1a , Recombinant Proteins , Severe Acute Respiratory Syndrome/drug therapy , Severe Acute Respiratory Syndrome/epidemiology , Severe Acute Respiratory Syndrome/virology , Vero Cells
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