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[嗜线虫致病杆菌中血腔杀虫剂Tp40的纯化与特性分析]

[Purification and characterization of the haemocoel insecticide Tp40 from Xenorhabdus nematophila].

作者信息

Yang Jun, Wang Qinying, Song Ping, Nangong Ziyan, Cui Long, Kong Fanfang, Feng Shanshan

机构信息

College of Plant Protection, Biocontrol Centre of Plant Diseases and Plant Pests of Hebei Province, Baoding, China.

出版信息

Wei Sheng Wu Xue Bao. 2008 May;48(5):677-83.

Abstract

OBJECTIVE

Xenorhabdus nematophila is an insect pathogen bacterium symbiotically associated with entomopathogenic nematode. The bacteria produce a number of toxins to overcome immune response of insect hosts and kill their hosts. We purified a novel haemocoel insecticidal protein from X. nematophila HB310, cloned and analysed gene sequence of this novel protein.

METHODS

We isolated and purified the insecticidal protein by methods of salting out and native-PAGE from the intracellular proteins of X. nematophila HB310. We tested the virulence of the protein by direct injection into fifth-instar Galleria mellonella larvae. The protein was identified by western blotting. The gene of insecticidal protein was cloned by PCR and analyzed in GenBank.

RESULTS

We purified a novel haemocoel insecticidal protein that was named as Tp40. The injectable hemocoelic potency (LD50) of Tp40 was 68.54 ng/larva against fifth-instar G. mellonella larvae. The SDS-PAGE spectrum of Tp40 only showed a single - 42kDa band. Western blotting with an antibody that was highly specific to the known Txp40 indicated that Tp40 was homologous to the known Txp40 and only existed inside cells. The nucleotide sequences of tp40 gene have been deposited in GenBank (accession number GenBank: EU095326). The size of the open reading frame of tp40 was 1107bp, encoding a peptide of 368 amino acid residues, with a theoretical molecular weight 41.5 kDa and an isoelectricpoint (IP) 8.66. The Tp40 shared 85%-99% homology of nucleotide sequences and 70%-99% amino acids with those of 13 group strains.

CONCLUSION

Tp40 is high injectable virulent for G. mellonella larvae and its gene/protein sequence is highly conserved, which play a key role during the bacterium-nematode killing host insects process.

摘要

目的

嗜线虫致病杆菌是一种与昆虫病原线虫共生的昆虫病原菌。该细菌产生多种毒素以克服昆虫宿主的免疫反应并杀死宿主。我们从嗜线虫致病杆菌HB310中纯化了一种新型血腔杀虫蛋白,克隆并分析了该新型蛋白的基因序列。

方法

我们通过盐析和非变性聚丙烯酰胺凝胶电泳(native-PAGE)方法从嗜线虫致病杆菌HB310的胞内蛋白中分离纯化杀虫蛋白。通过直接注射到五龄大蜡螟幼虫体内测试该蛋白的毒力。通过蛋白质免疫印迹法鉴定该蛋白。通过聚合酶链反应(PCR)克隆杀虫蛋白基因并在基因银行(GenBank)中进行分析。

结果

我们纯化了一种新型血腔杀虫蛋白,命名为Tp40。Tp40对五龄大蜡螟幼虫的注射血腔毒力(半数致死剂量,LD50)为68.54纳克/幼虫。Tp40的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)图谱仅显示一条单一的42 kDa条带。用对已知Txp40具有高度特异性的抗体进行蛋白质免疫印迹表明,Tp40与已知的Txp40同源,且仅存在于细胞内。tp40基因的核苷酸序列已存入基因银行(登录号GenBank:EU095326)。tp40的开放阅读框大小为1107bp,编码一个由368个氨基酸残基组成的肽段,理论分子量为41.5 kDa,等电点(IP)为8.66。Tp40与13个菌株组的核苷酸序列同源性为85%-99%,氨基酸同源性为70%-99%。

结论

Tp40对大蜡螟幼虫具有高注射毒力,其基因/蛋白序列高度保守,在细菌-线虫杀死宿主昆虫的过程中起关键作用。

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