# Integration of transcriptomics and metabolomics for understanding the global responses to neutral pH and high pH under high light in photosynthetic bacterium Rhodobacter alkalitolerans strain JA916T

**Authors:** Mohammad Yusuf Zamal, Sureshbabu Marriboina, Vijay Srinivas Lavudiya, Jerome Xavier Gunasekaran, Aprajita Kumari, Kapuganti Jagadish Gupta, Venkata Ramana Chintalapati, Rajagopal Subramanyam

PMC · DOI: 10.1128/aem.00932-25 · Applied and Environmental Microbiology · 2025-08-29

## TL;DR

This study explores how a photosynthetic bacterium adapts to high light and different pH levels by analyzing gene and metabolite responses.

## Contribution

The study identifies novel gene and metabolite markers linked to high-light and alkaline stress resilience in Rhodobacter alkalitolerans.

## Key findings

- Photosystem-related genes show higher expression under high light in both neutral and high pH conditions.
- Bacteriochlorophyll and carotenoid biosynthesis genes are more active in high pH, suggesting enhanced photoprotection.
- Metabolites like L-proline and putrescine correlate with stress response pathways under high light and pH.

## Abstract

Photosynthetic microorganisms are often exposed to fluctuating light intensities in their ecological niches. Rhodobacter alklitolerans is a versatile photosynthetic bacterium able to grow in alkaline conditions. Comprehensive analysis of transcriptomic and metabolomic data reveals preferential gene expression and metabolic regulation of R. alklitolerans strain JA916T to alkaline pH (hpH) to neutral pH (npH) growth conditions under high light intensities. The transcriptome analysis provided that the majority of the transcripts related to photosystems were found to increase their expression in both npH and hpH under high-light conditions compared to low light conditions. Interestingly, reaction center transcripts (pufH, pufM, and pufL) and light-harvesting complex transcripts (pufA and pufB, pucA and pucB) were upregulated one- to two fold more in npH with increasing light intensity conditions. However, bacteriochlorophyll (BChl) a and carotenoid biosynthesis genes were significantly upregulated in hpH. We also found higher expression of cell division transcripts in npH conditions (murG, ftsZ, ftsQ, and ftsA with 1- to 1.5-fold) than in hpH. Furthermore, the metabolome analysis showed a higher correlation among the physiologically important metabolites such as putrescine, phenylalanine, phytol, L-lysine, L-proline, β-alanine, citric acid, L—5 oxoproline, and Pentanedioic acid. These were found to be part of several important metabolic pathways, including porphyrin metabolism, responsible for BChl metabolism, amino acid metabolism, and the tricarboxylic acid (TCA) cycle, playing a crucial role in energy production, in osmotic balance, and maintaining redox balance caused by high light. The real-time PCR analysis revealed that TCA cycle pathway genes also showed higher expression levels in npH than in hpH conditions under high light. Overall, the current study identifies candidate genes, metabolites, and alkaline-dependent high-light stress defense mechanisms that could potentially enhance alkali and high-light resilience in R. alklitolerans strain JA916T.

The study provides detailed information about the differential transcriptomic and metabolic response of the photosynthetic bacterium R. alkalitolerans strain JA916T in alkaline and neutral pH conditions. The study puts emphasis on the core photosynthetic transcripts and how their expression level is lower in hpH compared to npH, especially when it is grown in high light. The study also reasons out the relatively higher expression of bacteriochlorophyll a and carotenoid biosynthesis pathway transcripts in hpH, emphasizing the more photoprotection in hpH growth conditions. Furthermore, it also explores the role of metabolites in the study under high light and pH conditions, such as L-proline, putrescine, phenylalanine, etc., and their intricate metabolic networks through correlation matrix and interaction networks. The high-light and alkali stress markers identified in our study from the photosynthetic bacterium R. alkalitolerans strain JA916T can be used to develop stress-tolerant strains.

## Linked entities

- **Genes:** pufM (photosynthetic reaction center subunit M) [NCBI Gene 6138854], pufL (photosynthetic reaction center subunit L) [NCBI Gene 6138855], PUM3 (pumilio RNA binding family member 3) [NCBI Gene 9933], pufB (light-harvesting antenna LH1, beta subunit) [NCBI Gene 6138857], pucA (xanthine dehydrogenase molybdopterin recruitment factor) [NCBI Gene 938865], pucB (putative molybdopterin cofactor synthesis cytidylyl transferase) [NCBI Gene 936486], murG (undecaprenyldiphospho-muramoylpentapeptide beta-N- acetylglucosaminyltransferase) [NCBI Gene 881264], ftsZ (cell division protein FtsZ) [NCBI Gene 857456], ftsQ (cell division protein FtsQ) [NCBI Gene 881322], ftsA (cell division protein FtsA) [NCBI Gene 881321]
- **Chemicals:** bacteriochlorophyll a (PubChem CID 11953947), carotenoid (PubChem CID 11227325), putrescine (PubChem CID 1045), phenylalanine (PubChem CID 994), phytol (PubChem CID 5280435), L-lysine (PubChem CID 5962), L-proline (PubChem CID 145742), β-alanine (PubChem CID 239), citric acid (PubChem CID 311), L—5 oxoproline (PubChem CID 7405), Pentanedioic acid (PubChem CID 743)

## Full-text entities

- **Genes:** PUM3 (pumilio RNA binding family member 3) [NCBI Gene 9933] {aka HA-8, HLA-HA8, KIAA0020, PEN, PUF-A, PUF6}
- **Chemicals:** phytol (MESH:D010836), porphyrin (MESH:D011166), L-5 oxoproline (MESH:D011761), L-lysine (MESH:D008239), Pentanedioic acid (-), L-proline (MESH:D011392), TCA (MESH:D014233), putrescine (MESH:D011700), citric acid (MESH:D019343), phenylalanine (MESH:D010649), carotenoid (MESH:D002338), beta-alanine (MESH:D015091)
- **Cell lines:** JA916T. — Homo sapiens (Human), Childhood B acute lymphoblastic leukemia, Cancer cell line (CVCL_8863)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12542759/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12542759/full.md

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Source: https://tomesphere.com/paper/PMC12542759