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基于转录组的圣诞岛红蟹(Gecarcoidea natalis)碳水化合物活性酶(CAZy)的鉴定,并呼吁将转录组衍生的甲壳动物 CAZys 纳入比较研究。

Transcriptome-Guided Identification of Carbohydrate Active Enzymes (CAZy) from the Christmas Island Red Crab, Gecarcoidea natalis and a Vote for the Inclusion of Transcriptome-Derived Crustacean CAZys in Comparative Studies.

机构信息

Centre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University, Geelong, VIC, 3220, Australia.

School of Science, Monash University Malaysia, Jalan Lagoon Selatan, 47500, Bandar Sunway, Selangor, Malaysia.

出版信息

Mar Biotechnol (NY). 2018 Oct;20(5):654-665. doi: 10.1007/s10126-018-9836-2. Epub 2018 Jul 11.

Abstract

The Christmas Island red crab, Gecarcoidea natalis, is an herbivorous land crab that consumes mostly fallen leaf litter. In order to subsist, G. natalis would need to have developed specialised digestive enzymes capable of supplying significant amounts of metabolisable sugars from this diet. To gain insights into the carbohydrate metabolism of G. natalis, a transcriptome assembly was performed, with a specific focus on identifying transcripts coding for carbohydrate active enzyme (CAZy) using in silico approaches. Transcriptome sequencing of the midgut gland identified 70 CAZy-coding transcripts with varying expression values. At least three newly discovered putative GH9 endo-β-1,4-glucanase ("classic cellulase") transcripts were highly expressed in the midgut gland in addition to the previously characterised GH9 and GH16 (β-1,3-glucanase) transcripts, and underscoring the utility of whole transcriptome in uncovering new CAZy-coding transcripts. A highly expressed transcript coding for GH5_10 previously missed by conventional screening of cellulase activity was inferred to be a novel endo-β-1,4-mannase in G. natalis with in silico support from homology modelling and amino acid alignment with other functionally validated GH5_10 proteins. Maximum likelihood tree reconstruction of the GH5_10 proteins demonstrates the phylogenetic affiliation of the G. natalis GH5_10 transcript to that of other decapods, supporting endogenous expression. Surprisingly, crustacean-derived GH5_10 transcripts were near absent in the current CAZy database and yet mining of the transcriptome shotgun assembly (TSA) recovered more than 100 crustacean GH5_10s in addition to several other biotechnological relevant CAZys, underscoring the unappreciated potential of the TSA database as a valuable resource for crustacean CAZys.

摘要

圣诞岛红蟹(Gecarcoidea natalis)是一种食草性陆蟹,主要以落叶枯枝为食。为了生存,G. natalis 需要发展出专门的消化酶,能够从这种饮食中提供大量可代谢的糖。为了深入了解 G. natalis 的碳水化合物代谢,我们进行了转录组组装,特别关注使用计算机方法鉴定编码碳水化合物活性酶(CAZy)的转录本。中肠腺的转录组测序鉴定了 70 个编码 CAZy 的转录本,它们的表达值各不相同。至少有三个新发现的假定 GH9 内切-β-1,4-葡聚糖酶(“经典纤维素酶”)转录本在中肠腺中高度表达,除了先前鉴定的 GH9 和 GH16(β-1,3-葡聚糖酶)转录本外,这突显了全转录组在揭示新的 CAZy 编码转录本方面的效用。一个高度表达的 GH5_10 编码转录本先前在纤维素酶活性的常规筛选中被忽略,被推断为 G. natalis 中的新型内切-β-1,4-甘露聚糖酶,从同源建模和与其他功能验证的 GH5_10 蛋白的氨基酸比对中得到了计算机支持。GH5_10 蛋白的最大似然树重建表明,G. natalis GH5_10 转录本与其他十足目动物的系统发育关系,支持内源性表达。令人惊讶的是,甲壳动物衍生的 GH5_10 转录本在当前的 CAZy 数据库中几乎不存在,但对转录组 shotgun 组装(TSA)的挖掘不仅恢复了 100 多个甲壳动物 GH5_10,还恢复了其他几个生物技术相关的 CAZys,这突显了 TSA 数据库作为甲壳动物 CAZys 有价值资源的未被充分认识的潜力。

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