Phaeobacter sp.菌株Y4I利用两个独立的细胞间通信系统来调节抗菌靛蓝素的产生。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
W Nathan Cude, Carson W Prevatte, Mary K Hadden, Amanda L May, Russell T Smith, Caleb L Swain, Shawn R Campagna, Alison Buchan
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引用次数: 19

摘要

当在生物膜或琼脂平板上生长时,海洋玫瑰杆菌Phaeobacter sps .菌株Y4I合成蓝色抗菌次级代谢物靛蓝素。先前的研究表明,靛蓝素的产生可能在一定程度上受细胞间通信系统的调节。Phaeobacter sp.菌株Y4I具有两个luxR和luxI同源的n -酰基- l-高丝氨酸内酯(n -酰基- l-高丝氨酸内酯(AHL))介导的细胞间通信系统,称为pgaRI和phaRI。我们在这里证明了Y4I产生两种优势的氨基酰基,新型单不饱和N-(3-羟基十二烯基)- l-高丝氨酸内酯(3OHC(12:1)- hsl)和相对常见的N-辛烷酰- l-高丝氨酸内酯(C8-HSL),并提供了它们分别由pha和PgaI合成的证据。任何一个基因位点的Tn5插入突变都会导致色素生成的消除(pgaR::Tn5)或减少(phaR::Tn5)。在这些突变背景中也观察到运动性缺陷和更致密的生物膜,表明这些系统的功能角色重叠。ahl的产生发生在琼脂表面生长的不同时间点,并通过同位素稀释高效液相色谱-串联质谱(ID-HPLC-MS/MS)分析确定。在表面接种2 h内,琼脂提取物中仅检测到3OHC(12:1)-HSL。随着表面附着细胞的建立(约10 h), 3OHC(12:1)-HSL的浓度下降,C8-HSL的浓度在14 h内迅速上升。经过较长时间(>24 h)的建立,3OHC(12:1)-HSL和C8-HSL的浓度分别上升并稳定在约15 nM和约600 nM。相比之下,在48小时内,靛蓝素的总量从无法检测到稳步增加到642 mh。AHL和靛蓝素合成酶(pgaI、phaI和igiD)的基因表达谱与它们的代谢产物谱一致。这些数据提供了pgaRI和phaRI在靛蓝素生物合成调控中发挥重叠作用的证据,并推测这使得Phaeobacter sp.菌株Y4I能够协调不同生长阶段依赖生理的靛蓝素生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phaeobacter sp. strain Y4I utilizes two separate cell-to-cell communication systems to regulate production of the antimicrobial indigoidine.

Phaeobacter sp. strain Y4I utilizes two separate cell-to-cell communication systems to regulate production of the antimicrobial indigoidine.

Phaeobacter sp. strain Y4I utilizes two separate cell-to-cell communication systems to regulate production of the antimicrobial indigoidine.

Phaeobacter sp. strain Y4I utilizes two separate cell-to-cell communication systems to regulate production of the antimicrobial indigoidine.

The marine roseobacter Phaeobacter sp. strain Y4I synthesizes the blue antimicrobial secondary metabolite indigoidine when grown in a biofilm or on agar plates. Prior studies suggested that indigoidine production may be, in part, regulated by cell-to-cell communication systems. Phaeobacter sp. strain Y4I possesses two luxR and luxI homologous N-acyl-L-homoserine lactone (AHL)-mediated cell-to-cell communication systems, designated pgaRI and phaRI. We show here that Y4I produces two dominantAHLs, the novel monounsaturated N-(3-hydroxydodecenoyl)-L-homoserine lactone (3OHC(12:1)-HSL) and the relatively common N-octanoyl-L-homoserine lactone (C8-HSL), and provide evidence that they are synthesized by PhaI and PgaI, respectively.A Tn5 insertional mutation in either genetic locus results in the abolishment (pgaR::Tn5) or reduction (phaR::Tn5) of pigment production. Motility defects and denser biofilms were also observed in these mutant backgrounds, suggesting an overlap in the functional roles of these systems. Production of the AHLs occurs at distinct points during growth on an agar surface and was determined by isotope dilution high-performance liquid chromatography–tandem mass spectrometry (ID-HPLC-MS/MS) analysis.Within 2 h of surface inoculation, only 3OHC(12:1)-HSL was detected in agar extracts. As surface-attached cells became established (at approximately 10 h), the concentration of 3OHC(12:1)-HSL decreased, and the concentration of C8-HSL increased rapidly over 14 h.After longer (>24-h) establishment periods, the concentrations of the two AHLs increased to and stabilized at approximately 15 nM and approximately 600 nM for 3OHC12:1-HSL and C8-HSL, respectively. In contrast, the total amount of indigoidine increased steadily from undetectable to 642 Mby 48 h. Gene expression profiles of the AHL and indigoidine synthases (pgaI, phaI, and igiD) were consistent with their metabolite profiles. These data provide evidence that pgaRI and phaRI play overlapping roles in the regulation of indigoidine biosynthesis, and it is postulated that this allows Phaeobacter sp. strain Y4I to coordinate production of indigoidine with different growth-phase-dependent physiologies.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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