ReviewArchives of microbiology2026
Harnessing engineered cyanobacteria for next-generation therapeutics.
Review in Archives of microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Next-Generation Cyanobacterial Biocontrol Agents for Crop Fungal Diseases: Molecular Mechanisms, Omics Insights, Applications, and Biosafety Considerations.Journal of basic microbiology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Cyanobacteria are among the oldest photoautotrophic organisms and are recognized as key producers of structurally diverse secondary metabolites with significant pharmacological relevance. These organisms synthesize a wide range of bioactive compounds, including anticancer, neuroactive, anti-inflammatory, and antimicrobial metabolites, many of which exhibit unique mechanisms of action. Despite this potential, practical exploitation of cyanobacterial metabolites has historically been limited by slow growth rates, low product yields, and the frequent transcriptional silence of biosynthetic gene clusters under laboratory conditions. Recent advances in synthetic biology and metabolic engineering have begun to address these challenges. Tools such as CRISPR-based genome regulation, modular cloning platforms, optogenetic control systems, and heterologous expression strategies now enable targeted activation, regulation, and optimization of cyanobacterial biosynthetic pathways. These approaches facilitate access to cryptic metabolites, improve pathway control, and enhance production efficiency, thereby increasing the programmability of cyanobacterial systems. This review integrates current knowledge of cyanobacterial metabolite diversity with recent developments in pathway engineering, regulatory control, and systems-level optimization. Comparative evaluation of microbial production hosts highlights that cyanobacteria are not universal replacements for established heterotrophic systems but occupy complementary niches where photoautotrophic growth, low-input cultivation, and sustainability provide strategic advantages. We further discuss emerging opportunities for decentralized and small-batch biomanufacturing, while critically examining key technical, biosafety, and regulatory barriers that constrain translational deployment. Overall, advances in synthetic biology are progressively transforming cyanobacteria from underexplored natural product sources into programmable platforms for sustainable, biomarker-guided, and precision-oriented therapeutic manufacturing. Continued integration of engineering tools, bioprocess optimisation, and regulatory frameworks will be essential to expand the translational potential of cyanobacterial systems.
Indexed as
Identifiers
41842959What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.