{"title":"铜诱导真菌BcLCC2漆酶基因转录。","authors":"U V A Buddhika, S Savocchia, C C Steel","doi":"10.1080/21501203.2020.1725677","DOIUrl":null,"url":null,"abstract":"<p><p>Laccases are one of many groups of inducible enzymes produced by the filamentous fungus, <i>Botrytis cinerea</i> during colonisation of host plant tissues. While the processes involved in laccase induction are not fully understood, Cupric ions (e.g. CuSO<sub>4</sub>) and gallic acid (GA) have been reported as laccase inducers. This study investigates laccases activities and the expression of three laccase genes (<i>BcLCC1, BcLCC2, BcLCC3</i>) in three <i>B. cinerea</i> isolates grown in laccase-inducing medium (LIM) supplemented with CuSO<sub>4</sub> and GA. Laccase activity in culture filtrates with CuSO<sub>4</sub> increased after 48 h of growth in LIM at 24°C. The induction of <i>BcLCC2</i> transcription was greatest at a concentration of 0.6 mM CuSO<sub>4</sub>, concentrations greater than 0.6 mM inhibited fungal growth. In contrast, no laccase induction was observed in the presence of GA. Liquid chromatography-mass spectroscopy (NanoLC ESI MS/MS) analysis confirmed the presence of a 63.4 kDa protein, the <i>BcLCC2</i> isoform in the culture filtrate with 0.6 mM CuSO<sub>4</sub>. Analysis of mRNA transcripts further showed <i>BcLCC3</i> was also inducible and the expression of <i>BcLCC2</i> and <i>BcLCC3</i> was isolate-dependent. In conclusion, CuSO<sub>4</sub> induces a 63.4 kDa laccase in <i>B. cinerea</i> by induced transcription of the <i>BcLCC2</i> gene.</p>","PeriodicalId":18833,"journal":{"name":"Mycology","volume":"12 1","pages":"48-57"},"PeriodicalIF":4.6000,"publicationDate":"2020-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/21501203.2020.1725677","citationCount":"13","resultStr":"{\"title\":\"Copper induces transcription of <i>BcLCC2</i> laccase gene in phytopathogenic fungus, <i>Botrytis cinerea</i>.\",\"authors\":\"U V A Buddhika, S Savocchia, C C Steel\",\"doi\":\"10.1080/21501203.2020.1725677\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Laccases are one of many groups of inducible enzymes produced by the filamentous fungus, <i>Botrytis cinerea</i> during colonisation of host plant tissues. While the processes involved in laccase induction are not fully understood, Cupric ions (e.g. CuSO<sub>4</sub>) and gallic acid (GA) have been reported as laccase inducers. This study investigates laccases activities and the expression of three laccase genes (<i>BcLCC1, BcLCC2, BcLCC3</i>) in three <i>B. cinerea</i> isolates grown in laccase-inducing medium (LIM) supplemented with CuSO<sub>4</sub> and GA. Laccase activity in culture filtrates with CuSO<sub>4</sub> increased after 48 h of growth in LIM at 24°C. The induction of <i>BcLCC2</i> transcription was greatest at a concentration of 0.6 mM CuSO<sub>4</sub>, concentrations greater than 0.6 mM inhibited fungal growth. In contrast, no laccase induction was observed in the presence of GA. Liquid chromatography-mass spectroscopy (NanoLC ESI MS/MS) analysis confirmed the presence of a 63.4 kDa protein, the <i>BcLCC2</i> isoform in the culture filtrate with 0.6 mM CuSO<sub>4</sub>. Analysis of mRNA transcripts further showed <i>BcLCC3</i> was also inducible and the expression of <i>BcLCC2</i> and <i>BcLCC3</i> was isolate-dependent. In conclusion, CuSO<sub>4</sub> induces a 63.4 kDa laccase in <i>B. cinerea</i> by induced transcription of the <i>BcLCC2</i> gene.</p>\",\"PeriodicalId\":18833,\"journal\":{\"name\":\"Mycology\",\"volume\":\"12 1\",\"pages\":\"48-57\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2020-02-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1080/21501203.2020.1725677\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mycology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/21501203.2020.1725677\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MYCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mycology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/21501203.2020.1725677","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 13
摘要
漆酶是丝状真菌灰霉病菌(Botrytis cinerea)在寄主植物组织定植过程中产生的众多诱导酶之一。虽然漆酶诱导的过程还不完全清楚,但铜离子(如CuSO4)和没食子酸(GA)已被报道为漆酶诱导剂。本研究研究了在添加CuSO4和GA的漆酶诱导培养基(LIM)中培养的3株灰绿芽孢杆菌的漆酶活性和3个漆酶基因(BcLCC1、BcLCC2、BcLCC3)的表达。在24°C条件下,添加CuSO4的培养滤液在LIM中生长48 h后,漆酶活性增加。浓度为0.6 mM的CuSO4对BcLCC2转录的诱导作用最大,浓度大于0.6 mM的CuSO4对真菌生长有抑制作用。相比之下,GA的存在没有观察到漆酶的诱导作用。液相色谱-质谱(NanoLC ESI MS/MS)分析证实,在0.6 mM CuSO4的培养滤液中存在63.4 kDa的BcLCC2蛋白异构体。mRNA转录本分析进一步表明BcLCC3也是可诱导的,并且BcLCC2和BcLCC3的表达是分离依赖的。综上所述,CuSO4通过诱导BcLCC2基因的转录,诱导出了一个63.4 kDa的漆酶。
Copper induces transcription of BcLCC2 laccase gene in phytopathogenic fungus, Botrytis cinerea.
Laccases are one of many groups of inducible enzymes produced by the filamentous fungus, Botrytis cinerea during colonisation of host plant tissues. While the processes involved in laccase induction are not fully understood, Cupric ions (e.g. CuSO4) and gallic acid (GA) have been reported as laccase inducers. This study investigates laccases activities and the expression of three laccase genes (BcLCC1, BcLCC2, BcLCC3) in three B. cinerea isolates grown in laccase-inducing medium (LIM) supplemented with CuSO4 and GA. Laccase activity in culture filtrates with CuSO4 increased after 48 h of growth in LIM at 24°C. The induction of BcLCC2 transcription was greatest at a concentration of 0.6 mM CuSO4, concentrations greater than 0.6 mM inhibited fungal growth. In contrast, no laccase induction was observed in the presence of GA. Liquid chromatography-mass spectroscopy (NanoLC ESI MS/MS) analysis confirmed the presence of a 63.4 kDa protein, the BcLCC2 isoform in the culture filtrate with 0.6 mM CuSO4. Analysis of mRNA transcripts further showed BcLCC3 was also inducible and the expression of BcLCC2 and BcLCC3 was isolate-dependent. In conclusion, CuSO4 induces a 63.4 kDa laccase in B. cinerea by induced transcription of the BcLCC2 gene.