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Robert Landick

Robert Landick

· Professor of Biochemistry

University of Wisconsin-Madison · Bacteriology

Active 1975–2027

h-index93
Citations26.0k
Papers32463 last 5y
Funding$20.2M1 active

Academic metrics are sourced from OpenAlex and public funding records; values may differ from Google Scholar.

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About

Robert Landick is a Professor of Biochemistry at the University of Wisconsin-Madison, within the Department of Bacteriology. He is based in the Microbial Sciences Building located at 1550 Linden Dr., Madison, WI 53706. As a faculty member, he is involved in research and teaching activities related to biochemistry and microbiology. His contact information includes a phone number (608) 265-8475 and an email address landick@bact.wisc.edu. Further details about his research focus, background, and key contributions are not provided on the page.

Research topics

  • Biology
  • Genetics
  • Cell biology
  • Computer Science
  • Molecular biology
  • Biochemistry
  • Computational biology
  • Chemistry
  • Virology

Selected publications

  • Structural basis for backtracking by the SARS-CoV-2 replication–transcription complex

    Proceedings of the National Academy of Sciences · 2021 · 121 citations

    Backtracking, the reverse motion of the transcriptase enzyme on the nucleic acid template, is a universal regulatory feature of transcription in cellular organisms but its role in viruses is not established. Here we present evidence that backtracking extends into the viral realm, where backtracking by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA-dependent RNA polymerase (RdRp) may aid viral transcription and replication. Structures of SARS-CoV-2 RdRp bound to the essentia…

  • Transcriptional Pausing as a Mediator of Bacterial Gene Regulation

    Annual Review of Microbiology · 2021 · 66 citations

    1st authorCorresponding

    Cellular life depends on transcription of DNA by RNA polymerase to express genetic information. RNA polymerase has evolved not just to read information from DNA and write it to RNA but also to sense and process information from the cellular and extracellular environments. Much of this information processing occurs during transcript elongation, when transcriptional pausing enables regulatory decisions. Transcriptional pauses halt RNA polymerase in response to DNA and RNA sequences and structures…

  • Crabtree/Warburg-like aerobic xylose fermentation by engineered Saccharomyces cerevisiae

    Metabolic Engineering · 2021 · 65 citations

    Bottlenecks in the efficient conversion of xylose into cost-effective biofuels have limited the widespread use of plant lignocellulose as a renewable feedstock. The yeast Saccharomyces cerevisiae ferments glucose into ethanol with such high metabolic flux that it ferments high concentrations of glucose aerobically, a trait called the Crabtree/Warburg Effect. In contrast to glucose, most engineered S. cerevisiae strains do not ferment xylose at economically viable rates and yields, and they requi…

  • Alternative transcription cycle for bacterial RNA polymerase

    Nature Communications · 2020 · 44 citations

    RNA polymerases (RNAPs) transcribe genes through a cycle of recruitment to promoter DNA, initiation, elongation, and termination. After termination, RNAP is thought to initiate the next round of transcription by detaching from DNA and rebinding a new promoter. Here we use single-molecule fluorescence microscopy to observe individual RNAP molecules after transcript release at a terminator. Following termination, RNAP almost always remains bound to DNA and sometimes exhibits one-dimensional slidin…

  • A majority of <i>Rhodobacter sphaeroides</i> promoters lack a crucial RNA polymerase recognition feature, enabling coordinated transcription activation

    Proceedings of the National Academy of Sciences · 2020 · 25 citations

    CarD levels when cells enter stationary phase, suggesting that reduced activation by CarD may contribute to inhibition of rRNA transcription when cells enter stationary phase, the stage of growth when bacterial ribosome synthesis declines.

Recent grants

Frequent coauthors

  • Rachel A. Mooney

    77 shared
  • Yaoping Zhang

    Southeast University

    76 shared
  • Joshua J. Coon

    Morgridge Institute for Research

    72 shared
  • Trey K. Sato

    Great Lakes Bioenergy Research Center

    69 shared
  • Seth A. Darst

    50 shared
  • Jessica M. Vera

    University of Wisconsin–Madison

    39 shared
  • Alexander S. Hebert

    University of Wisconsin–Madison

    38 shared
  • Patricia J. Kiley

    34 shared

Labs

Education

  • Ph.D., Microbiology

    University of Wisconsin-Madison

    1990
  • M.S., Microbiology

    University of Wisconsin-Madison

    1986
  • B.S., Microbiology

    University of Wisconsin-Madison

    1984

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