Microbiome differences in sugarcane and metabolically engineered oilcane accessions and their implications for bioenergy production.

Jihoon Yang, Thanwalee Sooksa-Nguan, Baskaran Kannan, Sofia Cano-Alfanar, Hui Liu, Angela Kent, John Shanklin, Fredy Altpeter, Adina Howe
{"title":"Microbiome differences in sugarcane and metabolically engineered oilcane accessions and their implications for bioenergy production.","authors":"Jihoon Yang, Thanwalee Sooksa-Nguan, Baskaran Kannan, Sofia Cano-Alfanar, Hui Liu, Angela Kent, John Shanklin, Fredy Altpeter, Adina Howe","doi":"10.1186/s13068-023-02302-6","DOIUrl":null,"url":null,"abstract":"<p><p>Oilcane is a metabolically engineered sugarcane (Saccharum spp. hybrid) that hyper-accumulates lipids in its vegetable biomass to provide an advanced feedstock for biodiesel production. The potential impact of hyper-accumulation of lipids in vegetable biomass on microbiomes and the consequences of altered microbiomes on plant growth and lipid accumulation have not been explored so far. Here, we explore differences in the microbiome structure of different oilcane accessions and non-modified sugarcane. 16S SSU rRNA and ITS rRNA amplicon sequencing were performed to compare the characteristics of the microbiome structure from different plant compartments (leaf, stem, root, rhizosphere, and bulk soil) of four greenhouse-grown oilcane accessions and non-modified sugarcane. Significant differences were only observed in the bacterial microbiomes. In leaf and stem microbiomes, more than 90% of the entire microbiome of non-modified sugarcane and oilcane was dominated by similar core taxa. Taxa associated with Proteobacteria led to differences in the non-modified sugarcane and oilcane microbiome structure. While differences were observed between multiple accessions, accession 1566 was notable in that it was consistently observed to differ in its microbial membership than other accessions and had the lowest abundance of taxa associated with plant-growth-promoting bacteria. Accession 1566 is also unique among oilcane accessions in that it has the highest constitutive expression of the WRI1 transgene. The WRI1 transcription factor is known to contribute to significant changes in the global gene expression profile, impacting plant fatty acid biosynthesis and photomorphogenesis. This study reveals for the first time that genetically modified oilcanes associate with distinct microbiomes. Our findings suggest potential relationships between core taxa, biomass yield, and TAG in oilcane accessions and support further research on the relationship between plant genotypes and their microbiomes.</p>","PeriodicalId":9125,"journal":{"name":"Biotechnology for Biofuels and Bioproducts","volume":"16 1","pages":"56"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064762/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology for Biofuels and Bioproducts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s13068-023-02302-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Oilcane is a metabolically engineered sugarcane (Saccharum spp. hybrid) that hyper-accumulates lipids in its vegetable biomass to provide an advanced feedstock for biodiesel production. The potential impact of hyper-accumulation of lipids in vegetable biomass on microbiomes and the consequences of altered microbiomes on plant growth and lipid accumulation have not been explored so far. Here, we explore differences in the microbiome structure of different oilcane accessions and non-modified sugarcane. 16S SSU rRNA and ITS rRNA amplicon sequencing were performed to compare the characteristics of the microbiome structure from different plant compartments (leaf, stem, root, rhizosphere, and bulk soil) of four greenhouse-grown oilcane accessions and non-modified sugarcane. Significant differences were only observed in the bacterial microbiomes. In leaf and stem microbiomes, more than 90% of the entire microbiome of non-modified sugarcane and oilcane was dominated by similar core taxa. Taxa associated with Proteobacteria led to differences in the non-modified sugarcane and oilcane microbiome structure. While differences were observed between multiple accessions, accession 1566 was notable in that it was consistently observed to differ in its microbial membership than other accessions and had the lowest abundance of taxa associated with plant-growth-promoting bacteria. Accession 1566 is also unique among oilcane accessions in that it has the highest constitutive expression of the WRI1 transgene. The WRI1 transcription factor is known to contribute to significant changes in the global gene expression profile, impacting plant fatty acid biosynthesis and photomorphogenesis. This study reveals for the first time that genetically modified oilcanes associate with distinct microbiomes. Our findings suggest potential relationships between core taxa, biomass yield, and TAG in oilcane accessions and support further research on the relationship between plant genotypes and their microbiomes.

Abstract Image

Abstract Image

Abstract Image

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
甘蔗和经过代谢工程改造的油甘蔗品种的微生物组差异及其对生物能源生产的影响。
油甘蔗是一种经过代谢工程改造的甘蔗(蔗属杂交种),可在其植物生物质中过度积累脂质,为生物柴油生产提供先进的原料。植物生物质中脂质的过度积累对微生物组的潜在影响,以及微生物组的改变对植物生长和脂质积累的后果,迄今为止还没有进行过探讨。在此,我们探讨了不同油甘蔗品种和非改良甘蔗微生物组结构的差异。通过 16S SSU rRNA 和 ITS rRNA 扩增子测序,比较了四个温室种植的油甘蔗品种和非改良甘蔗的不同植物区系(叶、茎、根、根瘤菌层和大体积土壤)的微生物组结构特征。仅在细菌微生物组中观察到显著差异。在叶片和茎干微生物群中,非改良甘蔗和油甘蔗整个微生物群的 90% 以上都由相似的核心类群主导。与变形菌相关的类群导致了非改良甘蔗和油甘蔗微生物组结构的差异。虽然多个样本之间存在差异,但值得注意的是,样本 1566 的微生物成员组成一直与其他样本不同,而且与促进植物生长的细菌相关的类群丰度最低。在油甘蔗品种中,编号 1566 也是独一无二的,因为它的 WRI1 转基因组成型表达量最高。众所周知,WRI1 转录因子会导致全球基因表达谱发生重大变化,影响植物脂肪酸的生物合成和光形态发生。这项研究首次揭示了转基因油菜与不同微生物群的关系。我们的研究结果表明了油甘蔗品种的核心类群、生物量产量和 TAG 之间的潜在关系,并支持进一步研究植物基因型与其微生物组之间的关系。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Alanine dehydrogenases from four different microorganisms: characterization and their application in L-alanine production. A high-throughput dual system to screen polyphosphate kinase mutants for efficient ATP regeneration in L-theanine biocatalysis. Unravelling and engineering an operon involved in the side-chain degradation of sterols in Mycolicibacterium neoaurum for the production of steroid synthons. Correction: Secretion of collagenases by Saccharomyces cerevisiae for collagen degradation. Engineering Saccharomyces cerevisiae for improved biofilm formation and ethanol production in continuous fermentation.
×
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