Carnivorous Nutrition in Pitcher Plants (Nepenthes spp.) via an Unusual Complement of Endogenous Enzymes

被引:41
|
作者
Lee, Linda [1 ,2 ]
Zhang, Ye [1 ,2 ]
Ozar, Brittany [1 ,2 ]
Sensen, Christoph W. [3 ]
Schriemer, David C. [1 ,2 ]
机构
[1] Univ Calgary, Dept Biochem & Mol Biol, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Southern Alberta Canc Res Inst, Calgary, AB T2N 4N1, Canada
[3] Graz Univ Technol, Inst Mol Biotechnol, A-8010 Graz, Austria
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
Nepenthes; transcriptomics; carnivory; mass spectrometry; fluid; enzymes; ASPARTIC PROTEASE NEPENTHESIN-1; EXCHANGE MASS-SPECTROMETRY; PROTEOME ANALYSIS; BIOLOGICAL FUNCTION; DIGESTIVE FLUID; UNIQUE MEMBER; ALATA BLANCO; EXPRESSION; PROTEINASES; CHITINASE;
D O I
10.1021/acs.jproteome.6b00224
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Plants belonging to the genus Nepenthes are carnivorous, using specialized pitfall traps called "pitchers" that attract, capture, and digest insects as a primary source of nutrients. We have used RNA sequencing to generate a cDNA library from the Nepenthes pitchers and applied it to mass spectrometry-based identification of the enzymes secreted into the pitcher fluid using a nonspecific digestion strategy superior to trypsin in this application. This first complete catalog of the pitcher fluid subproteome includes enzymes across a variety of functional classes. The most abundant proteins present in the secreted fluid are proteases, nucleases, peroxidases, chitinases, a phosphatase, and a glucanase. Nitrogen recovery involves a particularly rich complement of proteases. In addition to the two expected aspartic proteases, we discovered three novel nepenthensins, two prolyl endopeptidases that we name neprosins, and a putative serine carboxypeptidase. Additional proteins identified are relevant to pathogen-defense and secretion mechanisms. The full complement of acid-stable enzymes discovered in this study suggests that carnivory in the genus Nepenthes can be sustained by plant-based mechanisms alone and does not absolutely require bacterial symbiosis.
引用
收藏
页码:3108 / 3117
页数:10
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