Fermi calculations enable quick downselection of target genes and process optimization in photosynthetic systems.

IF 6.5 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2025-03-20 DOI:10.1093/plphys/kiaf103
Ratul Chowdhury, Wheaton Schroeder, Debolina Sarkar, Niaz Bahar Chowdhury, Supantha Dey, Rajib Saha
{"title":"Fermi calculations enable quick downselection of target genes and process optimization in photosynthetic systems.","authors":"Ratul Chowdhury, Wheaton Schroeder, Debolina Sarkar, Niaz Bahar Chowdhury, Supantha Dey, Rajib Saha","doi":"10.1093/plphys/kiaf103","DOIUrl":null,"url":null,"abstract":"<p><p>Understanding how photosynthetic organisms including plants and microbes respond to their environment is crucial for optimizing agricultural practices and ensuring food and energy security, particularly in the context of climactic change and sustainability. This perspective embeds back-of-the-envelope calculations across a photosynthetic organism design and scale up workflow. Starting from the whole system level, we provide a recipe to pinpoint key genetic targets, examine the logistics of detailed computational modeling, explore environmentally driven phenotypes, and feasibility as an industrial biofuel production chassis. While complex computer models or high throughput in vivo studies often dominate scientific inquiry, this perspective highlights the power of simple calculations as a valuable tool for initial exploration and evaluating study feasibility. Fermi calculations are defined as quick, approximate estimations made using back-of-the-envelope calculations and straightforward reasoning to achieve order-of-magnitude accuracy, named after the physicist Enrico Fermi. We show how Fermi calculations, based on fundamental principles and readily available data, can offer a first pass understanding of metabolic shifts in plants and microbes in response to environmental and genetic changes. We also discuss how Fermi checks can be embedded in data-driven advanced computing workflows to enable bio-aware machine learning. Lastly, an understanding of state-of-the-art is necessary to guide study feasibility and identifying key levers to maximize cost to return ratios. Combining biology- and resource- aware Fermi calculations, this proposed approach enables researchers to prioritize resource allocation, identify gaps in predictions and experiments, and develop intuition about how observed responses of plants differ between controlled laboratory environments and industrial conditions.</p>","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":" ","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf103","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Understanding how photosynthetic organisms including plants and microbes respond to their environment is crucial for optimizing agricultural practices and ensuring food and energy security, particularly in the context of climactic change and sustainability. This perspective embeds back-of-the-envelope calculations across a photosynthetic organism design and scale up workflow. Starting from the whole system level, we provide a recipe to pinpoint key genetic targets, examine the logistics of detailed computational modeling, explore environmentally driven phenotypes, and feasibility as an industrial biofuel production chassis. While complex computer models or high throughput in vivo studies often dominate scientific inquiry, this perspective highlights the power of simple calculations as a valuable tool for initial exploration and evaluating study feasibility. Fermi calculations are defined as quick, approximate estimations made using back-of-the-envelope calculations and straightforward reasoning to achieve order-of-magnitude accuracy, named after the physicist Enrico Fermi. We show how Fermi calculations, based on fundamental principles and readily available data, can offer a first pass understanding of metabolic shifts in plants and microbes in response to environmental and genetic changes. We also discuss how Fermi checks can be embedded in data-driven advanced computing workflows to enable bio-aware machine learning. Lastly, an understanding of state-of-the-art is necessary to guide study feasibility and identifying key levers to maximize cost to return ratios. Combining biology- and resource- aware Fermi calculations, this proposed approach enables researchers to prioritize resource allocation, identify gaps in predictions and experiments, and develop intuition about how observed responses of plants differ between controlled laboratory environments and industrial conditions.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
期刊最新文献
Time-course dual RNA-seq analyses and gene identification during early stages of plant-Phytophthora infestans interactions. Target of rapamycin signaling regulates starch degradation via α-glucan, water dikinase in a unicellular red alga. Membranous translation platforms in the chloroplast of Chlamydomonas reinhardtii. Hijacking Host Metabolism: PstEXLX1 Suppresses Triticum aestivum Defense responses by Targeting a Formate Dehydrogenase AtSRGA: A shiny application for retrieving and visualizing stress-responsive genes in Arabidopsis thaliana.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1