Deep-Sea Microbe Enrichment With Pressure-Driven Purification
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Solution Overview
Problem
Existing technologies face difficulties in purifying deep-sea microorganism samples under high-pressure environments, involve complex manual operations for enrichment and observation, and lack real-time cell counting capabilities, hindering the acquisition of high-purity enriched materials.
Innovation Solution
An online purification and sampling apparatus and visualized automatic enrichment apparatus are developed, incorporating units for temperature and pressure regulation, automatic biological concentration, online monitoring of environmental indicators, and real-time observation, enabling efficient separation and visualization of microbial samples under simulated deep-sea conditions.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Manufacturing precision
If conventional purification processes (washing, oscillation, centrifugation) are used under high-pressure environments, then sample processing can be performed, but purification effectiveness deteriorates due to difficulty in separating environmental impurities from microbial cells
Solution Approach 1:
The patent changes physical parameters by introducing a purification piston that applies mechanical pressure to the sample, forcing impurities through a filtration membrane. This pressure-driven separation mechanism overcomes the limitation of conventional low-pressure methods under high-pressure environmental conditions, achieving effective purification by utilizing pressure differential to separate microbial cells from environmental impurities.
Solution Approach 2:
The patent replaces conventional mechanical separation methods (washing, oscillation, centrifugation) with a piston-driven filtration system. The purification piston mechanically pushes the sample through a filtration membrane, providing a more effective separation mechanism that works reliably under high-pressure conditions where conventional methods fail to distinguish between microbial cells and environmental impurities.
2Measurement precision
If repeated periodic sampling and gene sequencing analysis are performed to observe microbial abundance, then quantitative data can be obtained, but operational complexity increases and timeliness decreases
Solution Approach 1:
The patent replaces manual sampling and gene sequencing analysis with an automated imaging system. The imaging system captures images of microbial cells in the culture chamber, and image analysis software automatically quantifies microbial abundance. This substitution eliminates the need for repeated manual sampling and sequencing operations, significantly reducing operational complexity while maintaining quantitative measurement capability and improving timeliness.
Solution Approach 2:
The patent creates a visual copy (image) of the microbial sample instead of physically sampling and sequencing it repeatedly. The imaging system captures optical images of the microbial cells, providing a permanent record that can be analyzed quantitatively without disturbing the sample. This copying approach allows repeated measurement without repeated physical intervention, reducing operational complexity and improving measurement timeliness.
3Adaptability or versatility
If manual operations are used for enrichment and observation, then flexibility can be maintained, but productivity decreases due to time-consuming processes
Solution Approach 1:
The patent implements self-service automation where the system performs enrichment and observation operations autonomously. The culture chamber maintains controlled conditions automatically, the imaging system captures images at predetermined intervals without manual intervention, and the system monitors environmental parameters autonomously. This self-service capability maintains operational flexibility through programmable control while dramatically improving productivity by eliminating time-consuming manual operations.
Solution Approach 2:
The patent enables continuous operation of the enrichment and observation process. The imaging system can capture images continuously or at predetermined intervals without interrupting the enrichment process, and the system can operate 24/7 without manual intervention. This continuity of useful action improves productivity by eliminating downtime associated with manual sampling and analysis, while flexibility is maintained through programmable control of imaging frequency and environmental conditions.
4Loss of time
If observation windows are used to view microbial samples, then real-time observation is possible, but cell counting becomes difficult due to excessive cell accumulation and overlapping cells
Solution Approach 1:
The patent uses imaging to create a copy (image) of the microbial sample for analysis. Instead of directly counting cells through the observation window where cells are densely packed and overlapping, the imaging system captures images that can be processed to identify and count individual cells. This copying approach allows real-time observation while improving measurement precision by enabling accurate cell counting from the captured images even when cells appear overlapping in the original sample.
Solution Approach 2:
The patent replaces direct visual observation and manual cell counting with an automated imaging and image analysis system. The imaging system captures digital images of the microbial cells, and software algorithms automatically identify, separate, and count cells based on their optical characteristics. This substitution maintains real-time observation capability while dramatically improving cell counting accuracy by eliminating the limitations of direct visual counting in dense microbial populations.
Applied Scientific Principles
This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.
Function Achieved in This Case
The apparatus facilitates automated pretreatment, real-time monitoring, and high-purity sample acquisition, improving the enrichment rate and efficiency of difficult-to-culture deep-sea microorganisms, enhancing deep-sea biological research and bioresource development.
Implementation Method 1
a pressure-retaining stirrer for mixing the sample under high pressure
Implementation Method 2
a pressure-retaining stirrer for mixing the sample under high pressure
Implementation Method 3
a purification piston for pressing the concentrated sample through a filtration membrane
Implementation Method 4
a purification piston for pressing the concentrated sample through a filtration membrane
Implementation Method 5
a purification piston for pressing the concentrated sample through a filtration membrane
Implementation Method 6
a general condition of the internal enriched material is mainly observed through a visualization window
Data Source
AI summary
The present invention provides an online purification and sampling and visualized automatic enrichment apparatus and method for deep-sea microorganisms. Through online sample pretreatment during microorganism sampling, automatic biological concentration and purification, online monitoring of environmental indicators during biological enrichment, online observation of biomass, and automatic enrichment and transfer of high-purity enriched materials, the present invention overcomes the shortcomings of the prior art, such as difficulties in purifying deep-sea microorganism samples under high-pressure environments, complex manual operations for enrichment and observation, low timeliness of biomass observation, and difficulties in real-time cell counting of the enriched materials. This effectively increases the enrichment rate and acquisition efficiency of difficult-to-culture deep-sea microorganisms, providing a fundamental way for enhancing deep-sea biological research and bioresource development efficiency.


