GET THE APP

Development of Genetically Engineered Microbial Biosensors
..

Biosensors & Bioelectronics

ISSN: 2155-6210

Open Access

Mini Review - (2024) Volume 15, Issue 1

Development of Genetically Engineered Microbial Biosensors

Serena Blake*
*Correspondence: Serena Blake, Department of Biomedical Engineering, Brown University, Providence, RI, USA, Email:
Department of Biomedical Engineering, Brown University, Providence, RI, USA

Received: 01-Feb-2024, Manuscript No. jbsbe-24-136729; Editor assigned: 02-Feb-2024, Pre QC No. P-136729; Reviewed: 16-Feb-2024, QC No. Q-136729; Revised: 22-Feb-2024, Manuscript No. R-136729; Published: 29-Feb-2024 , DOI: 10.37421/2155-6210.2024.15.430
Citation: Blake, Serena. “Development of Genetically Engineered Microbial Biosensors.” J Biosens Bioelectron 15 (2024): 430.
Copyright: © 2024 Blake S. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Genetically engineered biosensors represent a remarkable fusion of biology and engineering, where living organisms are purposefully modified to detect specific molecules or environmental conditions, converting this recognition into measurable signals. These biosensors offer a versatile platform for a wide range of applications, including environmental monitoring, medical diagnostics, industrial processes, and even biosecurity. At the heart of genetically engineered biosensors lies the genetic modification of living organisms, such as bacteria, yeast, or mammalian cells. These modifications involve the introduction of genes encoding sensing elements, which are typically proteins or genetic circuits designed to respond to the presence or concentration of a target molecule. The genetic material is integrated into the host organism's genome or maintained on plasmid vectors, ensuring heritable transmission of the engineered traits.

Keywords

Bacterial sensor • Microbial biosensors • Genetic modification

Introduction

Genetically engineered microbial biosensors represent a remarkable convergence of molecular biology, microbiology, and sensor technology, offering versatile platforms for the detection and quantification of a wide range of analytes in diverse environmental and industrial settings. These engineered microorganisms, often derived from bacteria, yeast, or other microbial species, are designed to exhibit specific responses to target analytes through the expression of genetically encoded sensing elements. Leveraging the natural metabolic pathways and regulatory networks of the host microorganism, these biosensors convert the presence of the target analyte into a measurable signal, providing valuable insights into environmental quality, industrial processes, and biological systems [1].

The development of genetically engineered microbial biosensors typically involves several key steps, including the selection of a suitable host organism, identification of sensing elements, genetic modification, and optimization of sensor performance. Each of these steps requires a deep understanding of microbial physiology, molecular biology techniques, and sensor engineering principles. Through iterative design, construction, and testing cycles, researchers can refine and enhance the sensitivity, specificity, and robustness of microbial biosensors for their intended applications [2].

Literature Review

The choice of host organism is a critical factor in the development of genetically engineered microbial biosensors, as it determines the genetic tools, growth conditions, and physiological characteristics available for sensor construction and operation. Bacteria such as Escherichia coli and Bacillus subtilis are commonly used as host organisms due to their well-characterized genetics, rapid growth rates, and ease of genetic manipulation. Yeasts such as Saccharomyces cerevisiae are also popular choices, particularly for applications in biotechnology and fermentation processes.

Once the host organism has been selected, the next step is to identify suitable sensing elements that can specifically recognize and respond to the target analyte. Sensing elements may include natural receptors, enzymes, transcription factors, or synthetic genetic circuits designed to produce a detectable output in response to the presence or concentration of the target analyte. For example, bacterial sensor proteins such as transcription factors or two-component systems can be engineered to respond to specific chemicals, ions, or environmental conditions [3].

Genetic modification of the host organism is then carried out to introduce the selected sensing elements and create the desired biosensor phenotype. This often involves the use of recombinant DNA techniques to insert the genes encoding the sensing elements into the microbial genome or plasmid vectors. Integration of the sensing elements into the host organism's regulatory network ensures that the biosensor responds appropriately to the target analyte while minimizing interference from other cellular processes.

Following genetic modification, the engineered microbial biosensor undergoes extensive characterization and optimization to evaluate its performance under different conditions and refine its sensitivity, specificity, and dynamic range. This may involve laboratory-based assays, high-throughput screening methods, or computational modeling approaches to assess the biosensor's response to varying concentrations of the target analyte and optimize its detection capabilities [4]. Throughout the development process, researchers must also consider factors such as biosafety, stability, and reproducibility to ensure the practical applicability of the microbial biosensor in real-world settings. Biosafety measures are essential to prevent unintended release or proliferation of the engineered microorganism and mitigate potential risks to human health and the environment. Strategies for biosafety may include containment protocols, genetic safeguards, and fail-safe mechanisms to prevent unintended consequences of biosensor deployment.

In addition to environmental and industrial applications, genetically engineered microbial biosensors hold great promise for biomedical and clinical use, particularly in the detection and monitoring of pathogens, toxins, and biomarkers associated with human health and disease. These biosensors can be tailored to detect specific pathogens or infectious agents in clinical samples, providing rapid and sensitive diagnostics for infectious diseases such as influenza, tuberculosis, and COVID-19.

Furthermore, microbial biosensors have the potential to revolutionize personalized medicine and precision healthcare by enabling real-time monitoring of biomarkers relevant to individual health status, disease progression, and treatment response. By integrating microbial biosensors with wearable devices, implantable sensors, or point-of-care diagnostic platforms, healthcare providers can obtain timely and actionable information to guide patient care decisions and optimize therapeutic outcomes.

Discussion

One of the key advantages of genetically engineered biosensors is their specificity, which can be finely tuned to target a particular analyte of interest. By selecting appropriate sensing elements, researchers can tailor biosensors to detect various chemicals, ions, gases, pathogens, or environmental conditions with high selectivity and sensitivity. For example, bacteria can be engineered to produce fluorescent proteins in response to specific toxins, allowing for visual detection under ultraviolet light.

The versatility of genetically engineered biosensors extends to their modularity, allowing for the construction of complex sensing systems from simple genetic components. Genetic circuits, such as transcriptional regulators, promoters, and reporter genes, can be combined and interconnected to create sophisticated signal transduction pathways that amplify and integrate the sensory input. This modularity enables the development of biosensors with customizable properties, including dynamic range, response time, and signal output [5,6].

Moreover, genetically engineered biosensors offer real-time monitoring capabilities, providing continuous, non-invasive insights into biological processes or environmental conditions. By coupling biosensors with readout technologies such as fluorescence microscopy, spectrophotometry, or electrochemical sensors, researchers can quantitatively measure the concentration or activity of the target analyte in real-time, facilitating rapid decision-making and intervention.

In environmental applications, genetically engineered biosensors are used to monitor pollution levels, assess water quality, detect hazardous chemicals, and track the spread of contaminants. Bacteria engineered to produce luminescent signals in the presence of heavy metals, for example, can be deployed in aquatic environments to identify sources of contamination and guide remediation efforts. Similarly, yeast strains modified to sense environmental toxins can serve as early warning systems for chemical spills or industrial accidents.

In medical diagnostics, genetically engineered biosensors offer sensitive and specific detection of disease biomarkers, pathogens, and therapeutic targets. Engineered mammalian cells equipped with surface receptors or intracellular signaling pathways can detect cancer-specific molecules in patient samples, providing early diagnosis and monitoring of disease progression. Similarly, viruses engineered to express reporter proteins in the presence of viral RNA or antigens enable rapid and sensitive detection of infectious agents, aiding in the control of epidemics and pandemics.

In industrial processes, genetically engineered biosensors play a crucial role in optimizing production efficiency, ensuring product quality, and minimizing environmental impact. Bacteria engineered to produce fluorescent proteins in response to specific nutrients or metabolic byproducts can be used to monitor fermentation processes in biotechnology and biofuel production. Similarly, yeast strains modified to detect contaminants in food or beverages help maintain product safety and compliance with regulatory standards.

Despite their tremendous potential, genetically engineered biosensors also pose challenges and considerations, including biosafety, biocontainment, and ethical implications. Strategies for mitigating these risks include the use of containment measures, genetic safeguards, and thorough risk assessments to ensure the safe and responsible deployment of engineered organisms. Additionally, ongoing research is needed to address technical challenges such as sensor stability, signal-to-noise ratio, and scalability to enable broader adoption and commercialization of genetically engineered biosensors.

Conclusion

In conclusion, the development of genetically engineered microbial biosensors represents a transformative approach to biosensing, with broad applications spanning environmental monitoring, industrial processes, biomedical research, and clinical diagnostics. By harnessing the genetic diversity and metabolic capabilities of microorganisms, researchers can engineer bespoke biosensors with tailored specificity, sensitivity, and functionality to address diverse challenges in science, technology, and medicine. As advances in molecular biology, synthetic biology, and sensor technology continue to drive innovation in this field, genetically engineered microbial biosensors are poised to play an increasingly prominent role in shaping the future of biosensing and biotechnology.

Acknowledgement

None.

Conflict of Interest

None.

References

  1. Rainina, E. I., E. N. Efremenco, S. D. Varfolomeyev and A. L. Simonian, et al. "The development of a new biosensor based on recombinant E. coli for the direct detection of organophosphorus neurotoxins." Biosens Bioelectron 11 (1996): 991-1000. 
  2. Google Scholar, Crossref, Indexed at

  3. Daunert, Sylvia, Gary Barrett, Jessika S. Feliciano and Ranjit S. Shetty, et al. "Genetically engineered whole-cell sensing systems: coupling biological recognition with reporter genes." Chem Rev 100 (2000): 2705-2738.
  4. Google Scholar, Crossref, Indexed at

  5. Shimazu, Mark, Ashok Mulchandani, and Wilfred Chen. "Simultaneous degradation of organophosphorus pesticides and p‐nitrophenol by a genetically engineered Moraxella sp. with surface‐expressed organophosphorus hydrolase." Biotechnology and Bioengineering 76 (2001): 318-324. 
  6. Google Scholar, Crossref, Indexed at

  7. Kumari, Anjali, Patrizia Pasini, Sapna K. Deo and Deborah Flomenhoft, et al. "Biosensing systems for the detection of bacterial quorum signaling molecules." Anal Chem 78 (2006): 7603-7609.
  8. Google Scholar, Crossref, Indexed at

  9. Kim, Jaewook, Sung Sik Woo, and Rahul Sarpeshkar. "Fast and precise emulation of stochastic biochemical reaction networks with amplified thermal noise in silicon chips." IEEE Trans Biomed Circuits And Sys 12 (2018): 379-389.
  10. Google Scholar, Crossref, Indexed at

  11. Gawrys, Michelle D., Izabela Hartman, Laura F. Landweber and David W. Wood. "Use of engineered Escherichia coli cells to detect estrogenicity in everyday consumer products." J Chem Technol Biotechnol 84 (2009): 1834-1840.
  12. Google Scholar, Crossref, Indexed at

Google Scholar citation report
Citations: 6207

Biosensors & Bioelectronics received 6207 citations as per Google Scholar report

Biosensors & Bioelectronics peer review process verified at publons

Indexed In

 
arrow_upward arrow_upward