Studies of the Enzyme D-Alanyl-D-Alanine Carboxypeptidase from Bacillus stearothermophilus

Structural Studies of the Enzyme D-Alanyl-D-Alanine Carboxypeptidase from Bacillus stearothermophilus, authored by Janet Frost, focuses on the comprehensive analysis of the structure and function of the enzyme D-alanyl-D-alanine carboxypeptidase. Frost is known for her research in biosynthesis, and her work sheds light on the crucial role played by this enzyme in bacterial cell wall biosynthesis. Furthermore, this enzyme has emerged as a pivotal target in developing antibiotics, thereby establishing the significance of this area of study.

Structural Studies of the Enzyme D-Alanyl-D-Alanine Carboxypeptidase from Bacillus stearothermophilus

Digital edition (English)
Authors	Janet Frost
Language	English
Subject	Muramoylpentapeptide carboxypeptidase, Geobacillus stearothermophilus
Publisher	University of Connecticut
Publication date	1994
Publication place	United States
Pages	106
OCLC	32137223

Background

The D-alanyl-D-alanine carboxypeptidase, also called DD-carboxypeptidase, is an enzyme pivotal to the final stages of peptidoglycan synthesis within bacterial cell walls. Its primary function is to catalyze the removal of D-alanyl-D-alanine dipeptide residues from peptidoglycan precursors, thereby upholding cell wall integrity. Bacillus stearothermophilus, a thermophilic bacterium, is an ideal model organism for researching this enzyme due to its stability and ease of cultivation.

Research and Methodology

Frost utilized a combination of X-ray crystallography, molecular modeling, and biochemical assays to achieve the study's objectives. The enzyme was expressed in Escherichia coli, purified using affinity chromatography, and crystallized for structural analysis. Data collected from X-ray diffraction experiments were used to solve the enzyme's structure, followed by a detailed analysis of the active site and interaction with inhibitors.

Findings and Implications

Janet Frost's dissertation presents an intricate analysis of the structural and functional aspects of DD-carboxypeptidase from Bacillus stearothermophilus, underscoring its significance in peptidoglycan synthesis and its potential as a target for antibiotic development. The outcomes carry substantial implications for formulating novel antibiotics and developing strategies to address antibiotic resistance, thus substantively contributing to the broader domains of microbiology and pharmaceutical science.

Key Findings

• High-Resolution Structure: The high-resolution crystal structure of D-alanyl-D-alanine carboxypeptidase (DD-carboxypeptidase) from Bacillus stearothermophilus was determined. This revealed the enzyme's characteristic fold and the detailed configuration of its active site.
• Active Site Characterization: Critical amino acid residues within the active site were identified. These residues are essential for substrate recognition and catalytic activity.
• Mechanism of Action: The study elucidated the enzyme's mechanism of action, demonstrating how it catalyzes the cleavage of D-alanyl-D-alanine dipeptide residues from peptidoglycan precursors.
• Inhibition by Beta-Lactam Antibiotics: Structural analysis showed that beta-lactam antibiotics inhibit the enzyme by mimicking its natural substrate, providing insights into the binding interactions between the enzyme and the antibiotics.

Implications

• Antibiotic Development: Understanding the structure and function of DD-carboxypeptidase is crucial for developing new antibiotics. The detailed structural information and mechanism of action can guide the design of drugs that more effectively target this enzyme.
• Combating Antibiotic Resistance: The research contributes to strategies for overcoming antibiotic resistance by revealing how beta-lactam antibiotics inhibit the enzyme. This knowledge can be used to modify existing antibiotics or develop new ones less susceptible to resistance mechanisms.
• Bacterial Cell Wall Biosynthesis: The findings enhance the broader understanding of bacterial cell wall biosynthesis. This can inform research on other enzymes involved in peptidoglycan synthesis, providing a comprehensive picture of this essential bacterial process.
• Model for Thermophilic Enzymes: Bacillus stearothermophilus, as a model organism, offers insights into the stability and functionality of thermophilic enzymes. This can have broader applications in industrial and biotechnological processes where enzyme stability at high temperatures is desirable.

Applications

Examining the D-alanyl-D-alanine carboxypeptidase (DD-carboxypeptidase) enzyme derived from Bacillus stearothermophilus, authored by Janet Frost, has yielded several practical applications across diverse fields.

Antibiotic Development

• Targeted Drug Design: An in-depth understanding of DD-carboxypeptidase's structural and functional aspects can be a blueprint for developing targeted antibiotics. Insight into how beta-lactam antibiotics hinder the enzyme's activity enables the creation of more potent drugs to combat bacterial infections.
• Overcoming Antibiotic Resistance: The research facilitates the modification of existing antibiotics to heighten their efficacy against resistant bacterial strains. Comprehending the enzyme's interaction with inhibitors lays the groundwork for developing drugs that are less prone to evoke bacterial resistance.

Bacterial Cell Wall Biosynthesis

• Peptidoglycan Research: The study significantly contributes to the broader comprehension of peptidoglycan biosynthesis within bacterial cell walls, thereby facilitating the identification of potential drug targets along the biosynthetic pathway.
• Functional Genomics: Researchers can use the structural data to explore the functions of similar enzymes in other bacterial species, enhancing the overall knowledge of bacterial physiology and cell wall maintenance.

Biotechnology and Industrial Applications

• Enzyme Engineering: Insights into the structure and stability of the thermophilic enzyme derived from Bacillus stearothermophilus can be leveraged in the field of enzyme engineering. This has the potential to facilitate the development of more resilient enzymes tailored for industrial applications necessitating elevated temperatures.
• Biocatalysis: The study can inform the development of biocatalysts for synthesizing specific chemical compounds, benefiting industries like pharmaceuticals, agriculture, and food processing.

Structural Biology and Biochemistry

• Structural Analysis Techniques: The methodologies utilized in the dissertation, such as X-ray crystallography and molecular modeling, serve as essential points of reference for researchers engaged in similar structural investigations of other proteins and enzymes.
• Active Site Engineering: Detailed knowledge of the active site can facilitate the engineering of enzymes with altered or improved catalytic properties for research and industrial applications.

Medical and Clinical Research

• Diagnostics: Understanding the structure and function of DD-carboxypeptidase can lead to the development of diagnostic tools for bacterial infections, especially those involving antibiotic-resistant strains.
• Therapeutic Interventions: The research establishes a framework for developing innovative therapeutic interventions targeting bacterial cell wall synthesis, potentially yielding new treatments for bacterial infections.

Education and Training

• Academic Curriculum: The methodologies and discoveries outlined in Frost's dissertation can seamlessly integrate into academic courses and training programs within biochemistry, microbiology, and structural biology. This integration provides students with a tangible demonstration of enzyme study and drug development research.

References

Works Cited

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External links

• Structural Studies of the Enzyme D-Alanyl-D-Alanine Carboxypeptidase from Bacillus stearothermophilus, 1994 Internet Archive