BSL2 or Biosafety Level 2 is a laboratory standard for moderately hazardous microorganisms. These organisms can harm humans, animals, plants or nature, but are typically not serious laboratory pathogens, or the prevention and treatment is in place already. BSL2 labs are mid-level of the biosafety level system between the low level BSL1 and the high level BSL3/BSL4.
Personal Protection, Equipment and Facilities, Laboratory Design, Waste Disposal, Training and Procedures — these are the major differences and improvements of BSL2 compared to BSL1. The risk of infection by contact with the skin or mucous membranes is higher in BSL2 labs because of the higher level of personal protection. Equipment and facilities in BSL2 laboratories, there is typically a biosafety cabinet for handling infectious samples, and an eyewash station and emergency shower. BSL2 in laboratory design, where the airflow must be controlled such that the air in the lab doesn't reach the outdoors thereby preventing pathogens from passing through. In the case of waste disposal, BSL2 laboratory waste must be completely sterilised and treated to ensure that bacteria don't make it to the environment as waste. Additionally, the personnel in BSL2 labs must be trained in higher levels of biosafety to know what the risks are and how to operate in the presence of moderately harmful pathogens.
BSL2 fermentation offers a number of different advantages for industries and research where BSL1 simply isn't enough biosafety. These benefits offer safety and efficacy for medium-risk microbes, which makes the door open for more sophisticated and multifarious applications. Specific Advantages are as follows:
Enhanced Safety and Compliance:
Broader Range of Applications:
Cost-Effective Solutions:
Cutting-Edge Equipment and Technical Expertise:
Quality Assurance and Support:
The utilization of BSL2 fermentation is marked by a diverse array of applications that address both current scientific needs and commercial demands. Generally, BSL2 fermentation serves pivotal roles in research, pharmaceuticals, and biotechnology by accommodating microorganisms and biological agents that pose moderate risks.
Through its strategic balance of safety and capability, BSL2 fermentation facilitates crucial advancements and innovation in several key domains, highlighting its importance in both present and future biotechnological landscapes. Meanwhile Creative BioMart Microbe continues to innovate in the field of fermentation, constantly developing excellent strains and efficient fermentation processes, and equipped with BSL2-level fermentation capabilities. Please feel free to contact us for more information about our BSL2 advanced fermentation.
Fermentation with BSL2 in the laboratory is typically used to create medium biosafety microbes or metabolites. What fermentation production can be produced in this type of laboratory is any of the following products:
Our services focus on ensuring the most suitable microorganisms are used in the fermentation process through professional BSL2-level strain selection and optimization. This includes utilizing the latest advances in metabolic engineering and synthetic biology. Our screening process not only includes natural selection and mutagenesis breeding, but also involves high-throughput screening technologies that can quickly identify and select strains with excellent performance. In addition, we also use genetic engineering methods such as CRISPR-Cas9 for precise gene editing to construct engineered strains with desired characteristics.
Our process control technology tracks the fermentation process from the moment of opening. Control parameters like pH, dissolved oxygen and carbon dioxide are set at the highest level to maintain the quality of the production environment and output of the products. Through online analytical instruments and tail gas analysis devices, we are able to measure the concentration and composition of the reaction solution in real time, predict reaction trends, and diagnose abnormal conditions. In addition, model-based control strategies and multivariate statistical modeling methods enable us to optimize the operation of the production system, thereby improving the formation efficiency and conversion rate of the target product.
In the pilot stage, we focus on developing and optimizing production processes, determining dominant strains and fermentation conditions, and simplifying equipment technical conditions and process flows. In the pilot stage, we will embody these processes in industrial production to verify the maturity and rationality of the synthetic process route, usually at a scale of 50-100 times that of the pilot, using the principle of step-by-step amplification. Finally, in the large-scale production stage, we achieve mass production of more than tons, involving the fermentation tank's piping system, stirring system, detection system, data analysis system, and feedback system, which work together to improve the fermentation process.
Case Study 1: Extraction of a particular protein by using yeast as the medium.
In one recent work, our group was able to use yeast fermentation to generate a target protein. The aim of the work was to show that yeast fermentation could produce high yield and high purity proteins that could be used in a therapeutic context. Expanded fermentation was run in a BSL2-controlled plant, which was safe and efficient. The fermentation parameters of pH, temperature and oxygen were precisely controlled for protein production. For ultrapurity, the crude extract was precipitated with ammonium sulphate, an age-old, efficient protein purification process. This precipitated the target protein, thus separating it from undesirable contaminants based on solubility differences. The precipitated protein was then downstream processed by dialysis and chromatography until the purity level was met.
Fig. 1. Ammonium sulfate precipitation.
Case Study 2: Efficient production of target protein using E. coli expression system.
In a new fermentation project, a new type of bioactive protein needs to be produced for drug development and clinical research. The protein has complex structure and function, requiring a high-yield and high-purity production process. We provide a full set of BSL2 solutions, using Escherichia coli expression system for the production of target proteins. By precisely controlling key steps such as transformation, induction expression, protein purification and renaturation, we ensure the successful expression and purification of the target protein. The results show that the target protein is efficiently expressed in the form of inclusion bodies in Rosetta (DE3) and BL21 (DE3) host strains, and the expression level increases with the increase of induction temperature. Through Ni-IDA-Sepharose CL-6B column purification and dialysis renaturation method, we obtained a high-purity soluble protein.
Fig. 2. SDS-PAGE analysis of dialyzed protein.
A: On the BSL2 level, we have medium-risk microorganisms, such as some pathogenic bacteria, viruses, etc, which can infect humans or animals but typically do have prevention and treatment.
A: Our BSL2 fermentation service can cover production needs from laboratory scale to pilot scale and then to industrial scale. We have the ability to perform small-scale experimental expression, and after optimizing the conditions, we can scale up to pilot scale and finally achieve large-scale production.
A: We follow strict procedures for handling and storing biological materials. All BSL2-level biological materials are handled in a biosafety cabinet to prevent cross contamination and exposure risks. When storing these materials, we use specialized equipment and a strict access system.
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