文献检索，用中文搜 PubMed

Suppr 超能文献

核心技术专利：CN118964589B侵权必究

核心技术专利：CN118964589B侵权必究

Hirigoyenberry F, Lassalle F, Lassegues M

Département de Physiologie des Invertébrés, Université de Bordeaux, Talence, France.

Comp Biochem Physiol B. 1990;95(1):71-5. doi: 10.1016/0305-0491(90)90250-w.

After bacterial infestation lysozyme and antibacterial activities are enhanced, peaking at 4 hr and 3 days, respectively. 2. Both humoral defenses require RNA and protein de novo synthesis in response to pathogenic bacteria injection (actinomycin D and cycloheximide experiments). 3. Antibacterial activity exists naturally at some basic level, involving regular translation of stable RNAs. 4. When antibacterial activity reaches its maximum after bacterial injection, proteins responsible for it undergo a turn-over. 5. Lysozyme and antibacterial proteins cannot account for the whole response to bacterial infestation; some cellular defense mechanisms like phagocytosis are involved at the same time.

细菌感染后，溶菌酶和抗菌活性增强，分别在4小时和3天达到峰值。2. 两种体液防御都需要响应致病性细菌注射（放线菌素D和环己酰亚胺实验）从头合成RNA和蛋白质。3. 抗菌活性在一定基础水平上自然存在，涉及稳定RNA的常规翻译。4. 细菌注射后抗菌活性达到最大值时，负责该活性的蛋白质会更新。5. 溶菌酶和抗菌蛋白不能解释对细菌感染的整个反应；同时还涉及一些细胞防御机制，如吞噬作用。

Hirigoyenberry F, Lassalle F, Lassegues M

Département de Physiologie des Invertébrés, Université de Bordeaux, Talence, France.

Comp Biochem Physiol B. 1990;95(1):71-5. doi: 10.1016/0305-0491(90)90250-w.

After bacterial infestation lysozyme and antibacterial activities are enhanced, peaking at 4 hr and 3 days, respectively. 2. Both humoral defenses require RNA and protein de novo synthesis in response to pathogenic bacteria injection (actinomycin D and cycloheximide experiments). 3. Antibacterial activity exists naturally at some basic level, involving regular translation of stable RNAs. 4. When antibacterial activity reaches its maximum after bacterial injection, proteins responsible for it undergo a turn-over. 5. Lysozyme and antibacterial proteins cannot account for the whole response to bacterial infestation; some cellular defense mechanisms like phagocytosis are involved at the same time.

细菌感染后，溶菌酶和抗菌活性增强，分别在4小时和3天达到峰值。2. 两种体液防御都需要响应致病性细菌注射（放线菌素D和环己酰亚胺实验）从头合成RNA和蛋白质。3. 抗菌活性在一定基础水平上自然存在，涉及稳定RNA的常规翻译。4. 细菌注射后抗菌活性达到最大值时，负责该活性的蛋白质会更新。5. 溶菌酶和抗菌蛋白不能解释对细菌感染的整个反应；同时还涉及一些细胞防御机制，如吞噬作用。