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首页> 外文期刊>Turkish journal of biology >Cloning and expression of chitinase A, B, and C (chiA, chiB, chiC) genes from Serratia marcescens originating from Helicoverpa armigera and determining their activities
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Cloning and expression of chitinase A, B, and C (chiA, chiB, chiC) genes from Serratia marcescens originating from Helicoverpa armigera and determining their activities

机译:来自棉铃虫的粘质沙雷氏菌几丁质酶A,B和C(chiA,chiB,chiC)基因的克隆和表达,并测定其活性

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Three genes encoding chitinase A (chiA), B (chiB), and C (chiC) were amplified from a bacterium that was isolated from a naturally dead Helicoverpa armigera larva and identified as Serratia marcescens based on 16S rRNA gene sequence analysis (KF823633 accession number). The open reading frames (ORFs) were identified as 1692, 1500, and 1443 base pairs for chiA, chiB, and chiC genes, respectively. These sequences were submitted to the GenBank with accession numbers KF823630 (chiA), KF823631 (chiB), and KF823632 (chiC). Comparison of the deduced amino acid sequences with those of other bacterial chitinases revealed that the 3 chitinases contain the catalytic domain. Furthermore, all 3 chitinases showed 99% similarity to the S. marcescens WW4 strain at the amino acid level. The chitinases were overexpressed in Escherichia coli. Expressed proteins were purified and their activities were tested using colloidal chitin as substrate. Reasonable pH and temperature ranges were also determined as 7-11 and 33-37 degrees C, respectively. Insecticidal activities of these proteins were tested on the larvae of Malacosoma neustria and H. armigera. Test results showed that 1000 U/mL ChiA, ChiB, and ChiC have 47%, 50%, and 66% insecticidal activities on M. neustria, and 80%, 45%, and 50% insecticidal activities on H. armigera larvae within 10 days, respectively.
机译:从一个自然死亡的棉铃虫幼虫中分离出的细菌中扩增了编码几丁质酶A(chiA),B(chiB)和C(chiC)的三个基因,并根据16S rRNA基因序列分析将其鉴定为粘质沙雷氏菌(KF823633登录号)。对于chiA,chiB和chiC基因,开放阅读框(ORF)分别被标识为1692、1500和1443个碱基对。这些序列以登录号KF823630(chiA),KF823631(chiB)和KF823632(chiC)提交给GenBank。推导的氨基酸序列与其他细菌几丁质酶的氨基酸序列的比较表明,这3个几丁质酶含有催化结构域。此外,所有3个几丁质酶在氨基酸水平上都显示出与Marcescens WW4菌株的99%相似性。几丁质酶在大肠杆菌中过表达。纯化表达的蛋白质,并使用胶体几丁质作为底物测试其活性。合理的pH和温度范围也分别确定为7-11和33-37摄氏度。这些蛋白质的杀虫活性已在新氏疟原虫和棉铃虫的幼虫上进行了测试。测试结果表明,在10毫克内,1000 U / mL ChiA,ChiB和ChiC对诺氏疟原虫具有47%,50%和66%的杀虫活性,对棉铃虫幼虫具有80%,45%和50%的杀虫活性。天分别。

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