东北农业大学学报
東北農業大學學報
동북농업대학학보
Journal of Northeast Agricultural University
2015年
10期
49-56
,共8页
马得莹%徐杨%李妍妍%徐倩倩%张婷婷%韩宗玺%刘胜旺
馬得瑩%徐楊%李妍妍%徐倩倩%張婷婷%韓宗璽%劉勝旺
마득형%서양%리연연%서천천%장정정%한종새%류성왕
鸡β-防御素12%重组蛋白%抗菌活性%组织分布
鷄β-防禦素12%重組蛋白%抗菌活性%組織分佈
계β-방어소12%중조단백%항균활성%조직분포
chickenβ-defensin 12%recombinant protein%antimicrobial activity%tissues distribution
为探讨鸡β-防御素12(AvBD12)的生物学特性,试验采用RT-PCR方法从鸡脾脏组织中扩增到鸡AvBD12基因,其cDNA大小为198 bp,编码65个氨基酸。将该基因亚克隆到大肠杆菌原核表达载体pProex HTa上,进行原核表达。Tricine-SDS-PAGE电泳表明,重组鸡AvBD12融合蛋白分子质量约为14 ku。对该重组蛋白进行纯化与体外抗菌活性的测定,结果显示,纯化后的重组鸡AvBD12融合蛋白对金黄色葡萄球菌和兔波氏杆菌有较高抗菌活性,对猪霍乱沙门氏菌和乳酸菌的抗菌活性较弱。高盐浓度对其抗菌活性有显著影响。该重组蛋白对鸡红细胞无显著溶血活性。荧光定量PCR结果表明,AvBD12基因在所测定的15个鸡组织器官中均有表达。
為探討鷄β-防禦素12(AvBD12)的生物學特性,試驗採用RT-PCR方法從鷄脾髒組織中擴增到鷄AvBD12基因,其cDNA大小為198 bp,編碼65箇氨基痠。將該基因亞剋隆到大腸桿菌原覈錶達載體pProex HTa上,進行原覈錶達。Tricine-SDS-PAGE電泳錶明,重組鷄AvBD12融閤蛋白分子質量約為14 ku。對該重組蛋白進行純化與體外抗菌活性的測定,結果顯示,純化後的重組鷄AvBD12融閤蛋白對金黃色葡萄毬菌和兔波氏桿菌有較高抗菌活性,對豬霍亂沙門氏菌和乳痠菌的抗菌活性較弱。高鹽濃度對其抗菌活性有顯著影響。該重組蛋白對鷄紅細胞無顯著溶血活性。熒光定量PCR結果錶明,AvBD12基因在所測定的15箇鷄組織器官中均有錶達。
위탐토계β-방어소12(AvBD12)적생물학특성,시험채용RT-PCR방법종계비장조직중확증도계AvBD12기인,기cDNA대소위198 bp,편마65개안기산。장해기인아극륭도대장간균원핵표체재체pProex HTa상,진행원핵표체。Tricine-SDS-PAGE전영표명,중조계AvBD12융합단백분자질량약위14 ku。대해중조단백진행순화여체외항균활성적측정,결과현시,순화후적중조계AvBD12융합단백대금황색포도구균화토파씨간균유교고항균활성,대저곽란사문씨균화유산균적항균활성교약。고염농도대기항균활성유현저영향。해중조단백대계홍세포무현저용혈활성。형광정량PCR결과표명,AvBD12기인재소측정적15개계조직기관중균유표체。
The objective of the study was to investigate bioactivity of chicken avian β-defensin (AvBD) 12 protein. AvBD12 gene was amplified from spleen tissue of chicken by RT-PCR. The cDNA of the gene consisted of 198 bp nucleotide, encoding a polypeptide of 65 amino acids. The cDNA was sub-cloned into pProex HTa vector and induced to express fusion protein. It was demonstrated by Tricine-SDS-PAGE that 14 ku protein was highly expressed. Antimicrobial activity of the recombinant fusion protein was measured in vitro. The recombinant protein exhibited high antimicrobial activity against Staphylococcus aureus and Bordetella bronchiseptica, low antimicrobial activity against Salmonell choleraesuis and Lactobacillus. The antibacterial activity of AvBD12 significantly decreased in high salt concentration. In addition, recombinant chicken AvBD12 showed little hemolytic activity against chicken erythrocytes. Results of real-time PCR showed that AvBD12 was widely expressed in all of the 15 tissues investigated.