Spampcin56-86 Peptide Synthesis for Antibacterial Efficacy

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Solution Overview

Problem

The overuse and misuse of antibiotics in China have led to significant bacterial resistance, compromised animal immunity, and ecological damage, necessitating the development of new and efficient antimicrobial alternatives.

Innovation Solution

The development of a novel antimicrobial peptide, Spampcin56-86 from Scylla paramamosain, with a specific amino acid sequence and chemical synthesis method, which exhibits broad-spectrum antibacterial and antifungal activity, and is used in preparing anti-bacterial agents, antifungal agents, and aquatic feed additives.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional antibiotics are used extensively, then bacterial infections are treated effectively, but bacterial resistance increases and ecological damage occurs

Engineering Contradiction:
Improveanti-bacterial efficacyVSAvoidbacterial resistance and ecological damage
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent changes the chemical structure parameters by designing and synthesizing peptide analogs with modified amino acid sequences (e.g., replacing natural amino acids with D-amino acids or non-natural amino acids), thereby altering the peptide's properties to overcome bacterial resistance while maintaining anti-bacterial efficacy

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates composite peptide structures by combining different amino acid sequences and modifications (e.g., N-terminal acetylation, C-terminal amidation, disulfide bridge formation) to produce peptides with enhanced and broad-spectrum anti-bacterial activity that does not induce resistance

Inventive Principle:
Principle #40Composite materials

2Adaptability or versatility

If new antimicrobial peptides are developed, then alternative anti-bacterial agents are provided, but synthesis complexity and cost increase

Engineering Contradiction:
Improvebroad-spectrum anti-microbial activityVSAvoidsynthesis process complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent segments the peptide synthesis process into modular steps using standard solid-phase peptide synthesis (SPPS) methodologies, allowing for systematic assembly of amino acid sequences and facilitating easier optimization and scaling of the synthesis process

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent optimizes synthesis parameters including solvent selection (e.g., using DMF, DCM, NMP), coupling reagents (e.g., HBTU, HATU, EDC), and purification conditions to improve yield and purity while reducing synthesis complexity and cost

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS12102086B2Antimicrobial peptide Spampcin<sub>56-86 </sub>from <i>Scylla paramamosain </i>and applications thereof
Publication Date: 2024.10.01 XIAMEN UNIV
  • US12102086B2 patent drawing
  • US12102086B2 patent drawing
  • US12102086B2 patent drawing

AI summary

An antimicrobial peptide Spampcin56-86from Scylla paramamosain is provided. A molecular formula of the antimicrobial peptide Spampcin56-86 is C154H256N54O33S3, and an amino acid sequence of the antimicrobial peptide Spampcin56-86 is shown in SEQ ID NO: 01.