Appl Environ Microbiol. 2026 Apr 16:e0239125. doi: 10.1128/aem.02391-25. Online ahead of print.
ABSTRACT
Bio-orthogonal non-canonical amino acid tagging (BONCAT) has emerged as a prominent molecular technique that enables microbial ecologists to visualize and identify metabolically active cells in cultures and complex microbial communities. To date, researchers have used just one non-canonical amino acid (ncAA) in a given experiment; here, we validate a novel approach using two different ncAAs in a single experiment. This advancement facilitates the detection of differentially active subpopulations within the same experimental context, thereby reducing the uncertainty and variability associated with parallel treatments and providing precise spatial information about organisms that are active under distinct conditions or at different times. We show that both ncAAs can be taken up by E. coli cultures and by constituents of the Little Sippewissett Salt Marsh microbiome, resulting in fluorescence signals that are significantly higher than background and ncAA-free control experiments, as well as differential labeling patterns reflective of distinct subpopulations. As a proof of concept, we implemented this “dual-BONCAT” approach in salt marsh sediments, adding one ncAA during daytime hours and the other at night. Subpopulations of cells that were anabolically active during the day and/or night were distinguishable by both fluorescence microscopy and by fluorescence-activated cell sorting. Subsequent high-throughput 16S rRNA gene amplicon sequencing of active subpopulations revealed that Methylobacterium, potentially feeding on plant exudate carbon, was preferentially active during the day, while sulfur-cycling taxa dominated the night-active population. Dual-BONCAT offers an important advancement in multiplexing substrate analog probing techniques, providing a more realistic understanding of metabolic activity under distinct environmental conditions.IMPORTANCEMicrobial communities are complex and dynamic, with different groups of microbes active under distinct conditions. Bio-orthogonal non-canonical amino acid tagging (BONCAT) uses synthetic amino acids to tag newly made proteins, allowing researchers to see and identify the active subset of a community. While BONCAT studies to date have used a single synthetic amino acid to evaluate cell activity in a single experimental context, here, we introduce a new approach, “dual-BONCAT,” using two synthetic amino acids to track differential responses to changing conditions. After validating the approach with E. coli, we deployed it in a salt marsh sediment community, finding that organisms potentially feeding on plant root sugars were more active during the day, while microbes likely metabolizing sulfur were more active at night. We believe dual-BONCAT will prove useful in many studies, as it illuminates microbial community responses to changing conditions, which has important implications for ecosystem dynamics.
- 微生物群集内の「活性な細胞」を可視化する手法BONCATに着目
- 従来は非天然アミノ酸(ncAA)1種類のみ使用 → 条件比較は別実験が必要
- 2種類のncAAを同時に用いる「dual-BONCAT」を開発・検証
- 同一サンプル内で異なる条件・時間の活性細胞を区別可能
- Escherichia coli および塩性湿地微生物群で取り込みと蛍光標識を確認
- 異なるサブポピュレーションが区別可能なラベリングパターンを示す
- 昼と夜で異なるncAAを添加 → 時間依存的な活性を可視化
- 顕微鏡およびセルソーティングで昼活性・夜活性細胞を分離
- 16S rRNA解析により、昼は Methylobacterium が優占的に活性
- 夜は硫黄代謝系微生物が優占
- 微生物群集内の時空間的な代謝活動を同時に追跡可能な手法を確立
- 1回の実験で「いつ・どの微生物が活性か」を同時に判別可能
- 並列実験に依存しないため、ばらつきや不確実性を低減
- 微生物群集の動的応答をより現実的に捉える手法として有用
PMID:41989202 | DOI:10.1128/aem.02391-25
BONCATの原理
- タンパク質合成中の細胞に着目 → “今まさに活動している細胞”を検出したい
- 非天然アミノ酸(ncAA:AHAやHPG)を培地に添加
- non-canonical amino acids (ncAAs) L-azidohomoalanine (AHA) and L-homopropargylglycine (HPG)
- これらはメチオニンの代わりに新規合成タンパク質へ取り込まれる
- ncAAにはアジド基・アルキン基を付加
- “クリックケミストリー”で蛍光分子を特異的に結合可能
- 新しく合成されたタンパク質だけが蛍光標識される
- タンパク質合成している細胞=代謝活性ありと判定
- 顕微鏡観察やFACSで活性細胞を可視化・分離
- その後、16S rRNA解析などで系統同定が可能
- 休眠細胞は標識されない → 活性サブポピュレーションのみ抽出可能
- “タンパク質を作っているかどうか”で活性を直接判定できる
- 群集内で「どの微生物が実際に働いているか」を特定可能
- 培養不要で環境中の微生物活性を解析できる