R
Ramesha B. Thimmappa
Researcher at Norwich Research Park
Publications - 8
Citations - 735
Ramesha B. Thimmappa is an academic researcher from Norwich Research Park. The author has contributed to research in topics: Triterpene & Sea cucumber. The author has an hindex of 5, co-authored 6 publications receiving 488 citations.
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Journal ArticleDOI
Triterpene Biosynthesis in Plants
TL;DR: Recent developments in the field of triterpene biosynthesis are reviewed, an overview of the genes and enzymes that have been identified to date are given, and strategies for discovering new triterpenes pathways are discussed.
Journal ArticleDOI
Sea cucumber genome provides insights into saponin biosynthesis and aestivation regulation.
Yuli Li,Ruijia Wang,Xiaogang Xun,Jing Wang,Lisui Bao,Ramesha B. Thimmappa,Jun Ding,Jingwei Jiang,Liheng Zhang,Tianqi Li,Jia Lv,Chuang Mu,Xiaoli Hu,Lingling Zhang,Jing Liu,Yuqiang Li,Lijie Yao,Wenqian Jiao,Yangfan Wang,Shanshan Lian,Zelong Zhao,Yaoyao Zhan,Xiaoting Huang,Huan Liao,Jia Wang,Hongzhen Sun,Xue Mi,Yu Xia,Qiang Xing,Wei Lu,Anne Osbourn,Zunchun Zhou,Yaqing Chang,Zhenmin Bao,Shi Wang +34 more
TL;DR: The sequencing and analysis of the genome and extensive transcriptomes of the sea cucumber Apostichopus japonicus are reported, a species from a special echinoderm group with extraordinary potential for saponin synthesis, aestivation and organ regeneration.
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Identification of key enzymes responsible for protolimonoid biosynthesis in plants: Opening the door to azadirachtin production.
Hannah E. Hodgson,Ricardo De La Peña,Michael J. Stephenson,Ramesha B. Thimmappa,Jason Leigh Vincent,Elizabeth S. Sattely,Elizabeth S. Sattely,Anne Osbourn +7 more
TL;DR: The characterization of protolimonoid biosynthetic enzymes from different plant species is reported and supports the notion of pathway conservation between both plant families.
Journal ArticleDOI
A conserved amino acid residue critical for product and substrate specificity in plant triterpene synthases
Melissa Salmon,Ramesha B. Thimmappa,Robert E. Minto,Rachel E. Melton,Richard K. Hughes,Paul E. O'Maille,Andrew M. Hemmings,Anne Osbourn +7 more
TL;DR: Mutation of this residue results in a major change in triterpene cyclization, with production of tetracyclic rather than pentacyclics products, and further open up opportunities to engineer novel oxygenated triterPene scaffolds by manipulating the precursor supply.
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Identification of key amino acid residues determining product specificity of 2,3-oxidosqualene cyclase in Oryza species.
Zheyong Xue,Zheyong Xue,Tan Zhengwei,Tan Zhengwei,Ancheng C. Huang,Yuan Zhou,Juncong Sun,Xiaoning Wang,Ramesha B. Thimmappa,Michael J. Stephenson,Anne Osbourn,Xiaoquan Qi +11 more
TL;DR: A promiscuous OSC from rice (Oryza sativa) (OsOS) is reported that synthesizes a novel pentacyclic triterpene orysatinol as its main product and reveals mechanistic insights into the cyclization of oxidosqualene into tetra- and pentacyClic skeletons, and provides a new strategy to identify key residues determining OSC specificity.