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Joseph S. Boyd

Researcher at University of California, San Diego

Publications -  19
Citations -  510

Joseph S. Boyd is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Circadian clock & KaiC. The author has an hindex of 13, co-authored 19 publications receiving 430 citations. Previous affiliations of Joseph S. Boyd include University of Redlands & University of Arizona.

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A protein fold switch joins the circadian oscillator to clock output in cyanobacteria

TL;DR: It is shown that KaiB flips between two distinct three-dimensional folds, and its rare transition to an active state provides a time delay that is required to match the timing of the oscillator to that of Earth’s rotation.
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Cross-talk and regulatory interactions between the essential response regulator RpaB and cyanobacterial circadian clock output.

TL;DR: The results suggest that regulatory interactions between RpaA and RpaB are required for transmission of updated time information to the level of gene expression, paving the way to uncover regulatory mechanisms involved in integration of temporal and environmental information.
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Asymmetric properties of the Chlamydomonas reinhardtii cytoskeleton direct rhodopsin photoreceptor localization.

TL;DR: Daughter four-membered rootlet microtubules direct eyespot positioning and assembly in H2O2-positive polyene-like structures, leading to high-performance liquid chromatography of Na6(CO3)(SO4)2, Na2SO4 and Na2CO3 in the H2S2 region.
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Giving Time Purpose: The Synechococcus elongatus Clock in a Broader Network Context.

TL;DR: The work that has established a global perspective of the clock is reviewed, with a focus on an emerging network-centric view of clock architecture, and mechanistic insights into how temporal and environmental cues are transmitted and integrated within this network.
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Active output state of the Synechococcus Kai circadian oscillator

TL;DR: A model that includes temporal feedback control of this KaiC phosphostate can accurately simulate key features of observed output responses of the two major contrasting promoter types, and finds evidence that phosphorylated RpaA (regulator of phycobilisome associated) represses an RPAA-independent output of KOA.