Ronglu Bai , Jingyi Xie , Yuna Zhang , LinLin Sun , Ziwei Zhang , Lizhi Wang , Jing Hu
{"title":"与二磷酸异戊烯基异构酶基因联用影响灵芝两种芳樟醇/神经醇合成酶同工型的表达","authors":"Ronglu Bai , Jingyi Xie , Yuna Zhang , LinLin Sun , Ziwei Zhang , Lizhi Wang , Jing Hu","doi":"10.1016/j.gene.2025.149394","DOIUrl":null,"url":null,"abstract":"<div><div>GlSTS21 and GsSTS41, derived from <em>Ganoderma lucidum</em> (Leyss. ex Fr.) Karst. and <em>G. sinense</em> Zhao, Xu et Zhang, respectively, have been identified as linalool/nerolidol synthases. Although both enzymes catalyze the synthesis of linalool and nerolidol, they exhibit distinct sequences and conserved structural domains, as well as variations in their secondary and tertiary structures, and differences in the location and number of substrate binding sites. When subjected to identical modification methods, GlSTS21 and GsSTS41 demonstrated divergent production trends. Specifically, GlSTS21 achieved the highest production of nerolidol when constructed in the sequence of pET28a-<em>T7</em>-<em>GlSTS21</em>-<em>T7</em>-<em>E. coli isopentenyl diphosphate isomerase (IDI)</em>. Conversely, the highest production of linalool by GlSTS21 occurred when it was arranged in the sequence of pET28a-<em>T7-GlSTS21-T7-E. coli IDI</em>. For GsSTS41, the optimal production of both linalool and nerolidol was attained when it was ligated in the sequence of pET28a-<em>T7</em>-<em>E. coli IDI</em>-<em>T7</em> −<em>GsSTS41</em>. These findings provide valuable insights for future efforts aimed at optimizing product-focused selection in industrial production processes.</div></div>","PeriodicalId":12499,"journal":{"name":"Gene","volume":"951 ","pages":"Article 149394"},"PeriodicalIF":2.4000,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Combination with isopentenyl diphosphate isomerase gene affects expression of two linalool/nerolidol synthases isoforms from Lingzhi\",\"authors\":\"Ronglu Bai , Jingyi Xie , Yuna Zhang , LinLin Sun , Ziwei Zhang , Lizhi Wang , Jing Hu\",\"doi\":\"10.1016/j.gene.2025.149394\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>GlSTS21 and GsSTS41, derived from <em>Ganoderma lucidum</em> (Leyss. ex Fr.) Karst. and <em>G. sinense</em> Zhao, Xu et Zhang, respectively, have been identified as linalool/nerolidol synthases. Although both enzymes catalyze the synthesis of linalool and nerolidol, they exhibit distinct sequences and conserved structural domains, as well as variations in their secondary and tertiary structures, and differences in the location and number of substrate binding sites. When subjected to identical modification methods, GlSTS21 and GsSTS41 demonstrated divergent production trends. Specifically, GlSTS21 achieved the highest production of nerolidol when constructed in the sequence of pET28a-<em>T7</em>-<em>GlSTS21</em>-<em>T7</em>-<em>E. coli isopentenyl diphosphate isomerase (IDI)</em>. Conversely, the highest production of linalool by GlSTS21 occurred when it was arranged in the sequence of pET28a-<em>T7-GlSTS21-T7-E. coli IDI</em>. For GsSTS41, the optimal production of both linalool and nerolidol was attained when it was ligated in the sequence of pET28a-<em>T7</em>-<em>E. coli IDI</em>-<em>T7</em> −<em>GsSTS41</em>. These findings provide valuable insights for future efforts aimed at optimizing product-focused selection in industrial production processes.</div></div>\",\"PeriodicalId\":12499,\"journal\":{\"name\":\"Gene\",\"volume\":\"951 \",\"pages\":\"Article 149394\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-06-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Gene\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378111925001829\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378111925001829","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/4 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Combination with isopentenyl diphosphate isomerase gene affects expression of two linalool/nerolidol synthases isoforms from Lingzhi
GlSTS21 and GsSTS41, derived from Ganoderma lucidum (Leyss. ex Fr.) Karst. and G. sinense Zhao, Xu et Zhang, respectively, have been identified as linalool/nerolidol synthases. Although both enzymes catalyze the synthesis of linalool and nerolidol, they exhibit distinct sequences and conserved structural domains, as well as variations in their secondary and tertiary structures, and differences in the location and number of substrate binding sites. When subjected to identical modification methods, GlSTS21 and GsSTS41 demonstrated divergent production trends. Specifically, GlSTS21 achieved the highest production of nerolidol when constructed in the sequence of pET28a-T7-GlSTS21-T7-E. coli isopentenyl diphosphate isomerase (IDI). Conversely, the highest production of linalool by GlSTS21 occurred when it was arranged in the sequence of pET28a-T7-GlSTS21-T7-E. coli IDI. For GsSTS41, the optimal production of both linalool and nerolidol was attained when it was ligated in the sequence of pET28a-T7-E. coli IDI-T7 −GsSTS41. These findings provide valuable insights for future efforts aimed at optimizing product-focused selection in industrial production processes.
期刊介绍:
Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.