A pseudoenzyme enables indole biosynthesis in eudicot plants

IF 13.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Matilde Florean, Hedwig Schultz, Veit Grabe, Katrin Luck, Grit Kunert, Sarah E. O’Connor, Tobias G. Köllner
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Abstract

Indole is an important biomolecule in plants, essential for amino acid biosynthesis, defense, pollinator attraction and plant–plant communication. Its biosynthesis is reported to be catalyzed by standalone indole-3-glycerol phosphate lyases, which are, however, absent in core eudicots. Here we show that, in core eudicots, indole production for defense and signaling occurs through an alternative pathway. The tryptophan synthase α subunit (TSA), which is typically complexed with the β subunit (TSB) to synthesize tryptophan through indole as an intermediate, can be hijacked by a noncatalytic paralog of TSB (TSB-like) to produce free indole. TSB-like is a pseudoenzyme that evolved from TSB by mutagenesis of two key essential residues, retaining the ability to allosterically activate TSA to allow formation and release of indole. The widespread occurrence and expression pattern of TSB-like genes in plants suggest that this is a general mechanism for the formation of free indole in plant defense and communication.

Abstract Image

一种假酶能使菊苣植物中的吲哚生物合成
吲哚是植物中一种重要的生物分子,在氨基酸生物合成、防御、吸引传粉者和植物间交流等方面具有重要作用。据报道,它的生物合成是由独立的吲哚-3-甘油磷酸裂解酶催化的,然而,在核心植物中是不存在的。在这里,我们表明,在核心诊断中,用于防御和信号传导的吲哚生产通过另一种途径发生。色氨酸合成酶α亚基(TSA)通常与β亚基(TSB)配合,通过吲哚作为中间体合成色氨酸,可被TSB的非催化类似物(TSB样)劫持,生成游离吲哚。TSB-like是一种假酶,由TSB通过诱变两个关键的基本残基进化而来,保留了变构激活TSA以形成和释放吲哚的能力。tsb样基因在植物中的广泛存在和表达模式表明,这是植物防御和通讯中游离吲哚形成的一般机制。
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来源期刊
Nature chemical biology
Nature chemical biology 生物-生化与分子生物学
CiteScore
23.90
自引率
1.40%
发文量
238
审稿时长
12 months
期刊介绍: Nature Chemical Biology stands as an esteemed international monthly journal, offering a prominent platform for the chemical biology community to showcase top-tier original research and commentary. Operating at the crossroads of chemistry, biology, and related disciplines, chemical biology utilizes scientific ideas and approaches to comprehend and manipulate biological systems with molecular precision. The journal embraces contributions from the growing community of chemical biologists, encompassing insights from chemists applying principles and tools to biological inquiries and biologists striving to comprehend and control molecular-level biological processes. We prioritize studies unveiling significant conceptual or practical advancements in areas where chemistry and biology intersect, emphasizing basic research, especially those reporting novel chemical or biological tools and offering profound molecular-level insights into underlying biological mechanisms. Nature Chemical Biology also welcomes manuscripts describing applied molecular studies at the chemistry-biology interface due to the broad utility of chemical biology approaches in manipulating or engineering biological systems. Irrespective of scientific focus, we actively seek submissions that creatively blend chemistry and biology, particularly those providing substantial conceptual or methodological breakthroughs with the potential to open innovative research avenues. The journal maintains a robust and impartial review process, emphasizing thorough chemical and biological characterization.
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