Development of in vitro lycopene biosynthesis from geranyl pyrophosphate employing cell-free protein synthesis

IF 2.5 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Young Hwan Goh, Ye Chan Kim, Sang Hun Jeong, Sangwoo Joo, You Kyoung Kwon, Hyunseok Yoon, Seohee Jung, Taresh P. Khobragade, Pritam Giri, Seonga Lim, Subin Yun, Sunga Cho, Sang Hyun Lee, Woo-Jae Chung, Jae Eun Lim, Taek Jin Kang, Hyungdon Yun
{"title":"Development of in vitro lycopene biosynthesis from geranyl pyrophosphate employing cell-free protein synthesis","authors":"Young Hwan Goh, Ye Chan Kim, Sang Hun Jeong, Sangwoo Joo, You Kyoung Kwon, Hyunseok Yoon, Seohee Jung, Taresh P. Khobragade, Pritam Giri, Seonga Lim, Subin Yun, Sunga Cho, Sang Hyun Lee, Woo-Jae Chung, Jae Eun Lim, Taek Jin Kang, Hyungdon Yun","doi":"10.1007/s12257-024-00111-8","DOIUrl":null,"url":null,"abstract":"<p>Lycopene is a compound classified as carotenoid, also known as tetraterpenoids, and its high antioxidative capabilities make demand in pharmaceutical and nutrient fields. For these reasons, much research on microbial production of lycopene has been developed and reported for more than two decades. Nevertheless, a standardized in vitro biosynthesis method for lycopene synthesis has not been reported to date. The major reasons of the absence of this method lie on the poor solubility of hydrophobic intermediates (geranylgeranyl pyrophosphate [GGPP] and phytoene), and the difficulty of employing membrane-binding enzyme, phytoene desaturase (CrtI) into in vitro reactions. In this study, we developed a standard method of in vitro biosynthesis of lycopene from geranyl pyrophosphate using four enzymes, namely farnesyl pyrophosphate synthase (IspA), GGPP synthase (CrtE), phytoene synthase (CrtB), phytoene desaturase (CrtI), and liposome-the key material, which can provide both hydrophobic area and a lipid membrane for the membrane-binding enzyme CrtI. Moreover, we performed a screening of the in vitro lycopene synthetic pathway using cell-free protein synthesis system, which verifies the applicability of our system as a tool for screening the lycopene synthesis pathway.</p>","PeriodicalId":8936,"journal":{"name":"Biotechnology and Bioprocess Engineering","volume":"43 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2024-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and Bioprocess Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s12257-024-00111-8","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Lycopene is a compound classified as carotenoid, also known as tetraterpenoids, and its high antioxidative capabilities make demand in pharmaceutical and nutrient fields. For these reasons, much research on microbial production of lycopene has been developed and reported for more than two decades. Nevertheless, a standardized in vitro biosynthesis method for lycopene synthesis has not been reported to date. The major reasons of the absence of this method lie on the poor solubility of hydrophobic intermediates (geranylgeranyl pyrophosphate [GGPP] and phytoene), and the difficulty of employing membrane-binding enzyme, phytoene desaturase (CrtI) into in vitro reactions. In this study, we developed a standard method of in vitro biosynthesis of lycopene from geranyl pyrophosphate using four enzymes, namely farnesyl pyrophosphate synthase (IspA), GGPP synthase (CrtE), phytoene synthase (CrtB), phytoene desaturase (CrtI), and liposome-the key material, which can provide both hydrophobic area and a lipid membrane for the membrane-binding enzyme CrtI. Moreover, we performed a screening of the in vitro lycopene synthetic pathway using cell-free protein synthesis system, which verifies the applicability of our system as a tool for screening the lycopene synthesis pathway.

Abstract Image

利用无细胞蛋白质合成技术,从焦磷酸香叶酯中开发体外番茄红素生物合成技术
番茄红素是一种类胡萝卜素化合物,也被称为四萜类化合物,它具有很强的抗氧化能力,因此在医药和营养品领域需求量很大。由于这些原因,二十多年来,有关微生物生产番茄红素的研究已经有了很多发展和报道。然而,迄今为止,还没有关于番茄红素合成的标准化体外生物合成方法的报道。缺乏这种方法的主要原因在于疏水性中间体(香叶基热原酰焦磷酸 [GGPP] 和植物烯)的溶解性较差,以及在体外反应中很难使用膜结合酶--植物烯去饱和酶(CrtI)。在本研究中,我们利用四种酶(焦磷酸芳萘酯合成酶(IspA)、焦磷酸GGPP合成酶(CrtE)、植物烯合成酶(CrtB)、植物烯去饱和酶(CrtI))和脂质体(关键材料),开发了一种体外生物合成焦磷酸香叶酯番茄红素的标准方法,脂质体可为膜结合酶CrtI提供疏水区域和脂膜。此外,我们还利用无细胞蛋白质合成系统对番茄红素的体外合成途径进行了筛选,从而验证了我们的系统作为番茄红素合成途径筛选工具的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biotechnology and Bioprocess Engineering
Biotechnology and Bioprocess Engineering 工程技术-生物工程与应用微生物
CiteScore
5.00
自引率
12.50%
发文量
79
审稿时长
3 months
期刊介绍: Biotechnology and Bioprocess Engineering is an international bimonthly journal published by the Korean Society for Biotechnology and Bioengineering. BBE is devoted to the advancement in science and technology in the wide area of biotechnology, bioengineering, and (bio)medical engineering. This includes but is not limited to applied molecular and cell biology, engineered biocatalysis and biotransformation, metabolic engineering and systems biology, bioseparation and bioprocess engineering, cell culture technology, environmental and food biotechnology, pharmaceutics and biopharmaceutics, biomaterials engineering, nanobiotechnology, and biosensor and bioelectronics.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信