# Screening and Evaluation of Chassis Cells for Heterologous Biosynthesis of Gas Vesicles as Ultrasound Contrast Agents

**Authors:** Qiuxia Fu, Kezhi Yu, Yuanyuan Wang, Chenxing Liu, Wei Liu, Wenze Ou, Wei Sun, Fei Yan

PMC · DOI: 10.3390/md24030106 · 2026-03-11

## TL;DR

This paper explores using different bacteria to produce gas vesicles for ultrasound imaging, aiming to find the best strain for high yield and performance.

## Contribution

The study provides experimental evidence on how different bacterial chassis cells affect gas vesicle production and function.

## Key findings

- Five bacterial strains were tested for gas vesicle production, with varying yields and imaging performance.
- The intracellular environment of chassis cells significantly influences gas vesicle morphology and function.

## Abstract

Gas vesicles (GVs) are hollow protein nanostructures derived from microorganisms and show significant potential for ultrasound imaging applications. However, the direct production of gas vesicles (GVs) from their native hosts faces several limitations: poor contrast imaging performance, insufficient yield, and high costs associated with extraction and purification. These challenges heavily hinder their clinical translation and application. The heterologous expression of GV genes varies significantly among different chassis strains due to their distinct intracellular environments, which ultimately affects GV performance and yield. Therefore, it is crucial to select an appropriate chassis cell that can produce GVs with excellent imaging performance. In this study, the GV gene cluster from Serratia sp. ATCC 39006 was heterologously expressed in five different bacterial chassis strains: Escherichia coli BL21 (AI), Escherichia coli K-12 MG1655, Escherichia coli Nissle 1917, Salmonella YB1, and Vibrio natriegens. By systematically comparing the yield, particle morphology, and ultrasound imaging performance of GVs produced by these strains, we elucidated the impact of chassis cells on GV synthesis and function. This work provides experimental evidence and theoretical support for screening robust GV-producing strains and facilitates future biomedical applications of GVs.

## Linked entities

- **Species:** Escherichia coli Nissle 1917 (taxon 316435), Vibrio natriegens (taxon 691)

## Full-text entities

- **Genes:** Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Dnase1 (deoxyribonuclease I) [NCBI Gene 13419] {aka DNaseI, Dnl1}
- **Diseases:** liver (MESH:D017093), liver diseases (MESH:D008107), Tumor (MESH:D009369), toxicity (MESH:D064420), injury to (MESH:D014947), GVs (MESH:C567751)
- **Chemicals:** kanamycin (MESH:D007612), glucose (MESH:D005947), NaCL (MESH:D012965), PBS (MESH:D007854), penicillin (MESH:D010406), H&amp;E (MESH:D006371), DAPI (MESH:C007293), agar (MESH:D000362), agarose (MESH:D012685), GV (-), streptomycin (MESH:D013307)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], uncultured marine bacterium (species) [taxon 56765], Vibrio natriegens (species) [taxon 691], Homo sapiens (human, species) [taxon 9606], Escherichia coli str. K-12 substr. MG1655 (no rank) [taxon 511145], Escherichia coli BL21 (strain) [taxon 511693], Serratia sp. (in: enterobacteria) (species) [taxon 616], Mus musculus (house mouse, species) [taxon 10090], Escherichia coli Nissle 1917 (strain) [taxon 316435], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW), GVMG1655 — Homo sapiens (Human), Maple syrup urine disease, Transformed cell line (CVCL_D514), B16F10 — Mus musculus (Mouse), Mouse melanoma, Cancer cell line (CVCL_0159), BL21 — Homo sapiens (Human), EBV-related Burkitt lymphoma, Cancer cell line (CVCL_M639), ATCC 39006 — Homo sapiens (Human), Finite cell line (CVCL_LK64), EcN — Homo sapiens (Human), Transformed cell line (CVCL_9I02), AI — Mus musculus (Mouse), Hybridoma (CVCL_C5HW)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027821/full.md

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Source: https://tomesphere.com/paper/PMC13027821