2,129 research outputs found
An Account of the Species of the Red Alga Herposiphonia Occurring in the Central and Western Tropical Pacific Ocean
Fourteen species of the genus Herposiphonia are described. The following
species and varieties are new: H. armata, H. crassa, H. delicatula, H. dendroidea,
H. dendroidea var. minor, H. dubia, H. nuda, H. obscura, H. parca var.
interrupta, H. pacifica, H. trichia, H. variabilis. The distributional range is extended
for H. parca, H. subdisticha, and H. tenella. H. secunda is reduced to a form of
H. tenella.
Emphasis is given to the nature and arrangement of trichoblasts and of sexual
reproductive structures as features of taxonomic importance
Quantum gate for Q switching in monolithic photonic bandgap cavities containing two-level atoms
Photonic bandgap cavities are prime solid-state systems to investigate
light-matter interactions in the strong coupling regime. However, as the cavity
is defined by the geometry of the periodic dielectric pattern, cavity control
in a monolithic structure can be problematic. Thus, either the state coherence
is limited by the read-out channel, or in a high Q cavity, it is nearly
decoupled from the external world, making measurement of the state extremely
challenging. We present here a method for ameliorating these difficulties by
using a coupled cavity arrangement, where one cavity acts as a switch for the
other cavity, tuned by control of the atomic transition.Comment: 6 pages, 5 figures, 1 tabl
Defining the Structural Consequences of Mechanism-Based Inactivation of Mammalian Cytochrome P450 2B4 Using Resonance Raman Spectroscopy
In view of the potent oxidizing strength of cytochrome P450 intermediates, it is not surprising that certain substrates can give rise to reactive species capable of attacking the heme or critical distal-pocket protein residues to irreversibly modify the enzyme in a process known as mechanism-based (MB) inactivation, a result that can have serious physiological consequences leading to adverse drug−drug interactions and toxicity. While methods exist to document the attachment of these substrate fragments, it is more difficult to gain insight into the structural basis for the altered functional properties of these modified enzymes. In response to this pressing need to better understand MB inhibition, we here report the first application of resonance Raman spectroscopy to study the inactivation of a truncated form of mammalian CYP2B4 by the acetylenic inhibitor 4-(tert-butyl)phenylacetylene, whose activated form is known to attach to the distal-pocket T302 residue of CYP2B4
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