# Analysis of Metabolic Capabilities of Prokaryotic Cells

> **NIH NIH R35** · UNIVERSITY OF GEORGIA · 2020 · $681,421

## Abstract

Program Director/Principal Investigator (Last, First, Middle): Escalante, Jorge C.
PROJECT SUMMARY/ABSTRACT
 This MIRA proposal brings together two fields of prokaryotic metabolism and physiology that the PI’s group
has contributed extensively to. The first is the assembly of the structurally complex coenzyme B12 (CoB12), and
the second one is the regulation of protein function by lysine acetylation in response to metabolic stress.
Previous work by the PI’s group in these areas has resulted in the discovery of new enzymes and pathways,
and has established fundamental physiologic paradigms that apply to cells of all domains of life.
 We have learned a great deal about how the complex coenzyme B12 is made, and yet, gaps in our knowledge
about its assembly remain. Although the remaining gaps are challenging to solve, recent breakthroughs in our
group have generated the tools to address these questions and advance our understanding of the
physiological integration of CoB12 biosynthesis in microorganisms of societal importance. We will investigate
how the lower ligand base of CoB12 is synthesized and activated to its riboside in human pathogens, how
vitamin B12 is converted to CoB12 in several Gram-positive pathogens, and why the last steps of the pathway
occur at the cell membrane in all CoB12 producers known to date. Most of the proposed work will be performed
in Salmonella enterica because of our deep knowledge of CoB12 biosynthesis in this bacterium, and the
sophisticated genetic system available to do in vivo work. We will also use Salmonella to establish the function
of heterologous, putative CoB12 biosynthetic functions in other bacteria and archaea.
 We will continue to investigate the role of lysine acetylation in the control of metabolic stress. Lysine
acetylation is a posttranslational modification of profound relevance to human health and biotechnology. The
impact of this regulatory mechanism on human cell aging and cancer, neurodegenerative diseases, diabetes,
obesity, antimicrobial resistance, microbial pathogenesis, and other research areas of societal relevance
emphasizes the need to continue advancing this field of research. Fundamental questions about lysine
acetylation remain unanswered. The proposed work will investigate new role(s) of prokaryotic sirtuin
deacetylases in prokaryotic physiology, and will continue to elucidate the functions and physiological roles of
acetyltransferases in Gram-negative and Gram-positive human pathogens. Our findings obtained from
experiments performed with prokaryotic model organisms will inform how the system may work in higher forms
of life.
 A powerful, innovative combination of approaches, including transition metal spectroscopy, structural biology
(crystallography), biochemistry, molecular biology, in vivo genetics, physiology, single-molecule biophysics,
and system-wide analyses will be applied during the performance of the proposed work. We will collaborate
with experts in the fields of spectr...

## Key facts

- **NIH application ID:** 9873055
- **Project number:** 5R35GM130399-02
- **Recipient organization:** UNIVERSITY OF GEORGIA
- **Principal Investigator:** JORGE C ESCALANTE
- **Activity code:** R35 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $681,421
- **Award type:** 5
- **Project period:** 2019-03-01 → 2024-02-29

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9873055

## Citation

> US National Institutes of Health, RePORTER application 9873055, Analysis of Metabolic Capabilities of Prokaryotic Cells (5R35GM130399-02). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/9873055. Licensed CC0.

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