Discovery of the female of Pyrocoelia prolongata in Taiwan (Coleoptera, Lampyridae)

The female of Pyrocoelia prolongata Jeng & Lai, a diurnal lampyrid species from Taiwan, is described for the first time. A single individual was found in a small, shady, dry streambed at the edge of a mixed forest at 2700 m elevation. The individual glowed in darkness and would move its abdomen up and down when disturbed and as a deterring behavior. A key to the females of the species of Pyrocoelia Gorham in Taiwan is provided. The morphology of photogenic organs of females and the function of bioluminescence of day-active species of Pyrocoelia are discussed.     

中国萤火虫云南窗萤荧光素酶cDNA的克隆表达和序列分析

从一种来自中国日行性萤火虫(云南窗萤)发光器官mRNA中克隆、测序并表达了有功能的荧光素酶.云南窗萤荧光素酶的cDNA序列有1647个碱基,编码548个氨基酸残基.从推测得到的氨基酸序列的比对分析得出:云南窗萤的荧光素酶与来自Lampyris noctiluca,L.turkestanicus和Nyctophila cf.caucasica三种萤火虫的荧光素酶有97.8%的序列一致性.从推测得出的氨基酸序列进行系统发育分析,其结果表明:云南窗萤和Lampyris Nyctophila聚在一起,与同属的发光强夜行性的萤火虫不形成的单系.云南窗萤荧光素酶在大肠杆菌中表达的条带大约70kDa,并且在有荧光素存在时发出黄绿色荧光.对荧光素酶的结构模拟和分析表明,云南窗萤荧光素酶基因的氨基端和羧基端结构域之间的裂沟处存在这5个多肽环,这正是从其他荧光素酶推测得到的催化荧光反应时的底物结合位点.云南窗萤和窗萤属的其他3种萤火虫的荧光素酶卡目比,有13个不同氨基酸位点,位于模拟分子结构的表面.对于这些多肽环、不刚氨基酸残基和晶体结构的进一步研究有利于解释日行和夜行性萤火虫荧光素酶的差异.     

中国萤火虫云南窗萤荧光素酶cDNA的克隆表达和序列分析(英文）

从一种来自中国日行性萤火虫（云南窗萤）发光器官mRNA中克隆、测序并表达了有功能的荧光素酶。云南窗萤荧光素酶的cDNA序列有1 647个碱基,编码548个氨基酸残基。从推测得到的氨基酸序列的比对分析得出：云南窗萤的荧光素酶与来自Lampyris noctiluca, L. turkestanicus和Nyctophila cf. caucasica三种萤火虫的荧光素酶有97.8%的序列一致性。从推测得出的氨基酸序列进行系统发育分析,其结果表明：云南窗萤和Lampyris+Nyctophila聚在一起, 与同属的发光强夜行性的萤火虫不形成的单系。云南窗萤荧光素酶在大肠杆菌中表达的条带大约70 kDa,并且在有荧光素存在时发出黄绿色荧光。对荧光素酶的结构模拟和分析表明,云南窗萤荧光素酶基因的氨基端和羧基端结构域之间的裂沟处存在这5个多肽环,这正是从其他荧光素酶推测得到的催化荧光反应时的底物结合位点。云南窗萤和窗萤属的其他3种萤火虫的荧光素酶相比,有13个不同氨基酸位点,位于模拟分子结构的表面。对于这些多肽环、不同氨基酸残基和晶体结构的进一步研究有利于解释日行和夜行性萤火虫荧光素酶的差异。     

云南窗萤的形态学及其生物学特性（鞘翅目：萤科）

研究了云南窗萤卵到成虫不同发育阶段的形态学。根据野外观察和实验室饲养结果,记录了其生物学特性。卵、幼虫、蛹和雌成虫可发弱光,但雄成虫仅在受刺激时才发出更弱的光,云南窗萤可归属于昼行性萤火虫,而化学信号则是其雌雄在求偶时的主要识别方式。     

窗胸萤肠道细菌分离及鉴定研究

从窗胸萤的5龄幼虫中分离纯化获得10个细菌菌株,并对其菌体形态、染色反应、培养性状、生理生化性状进行了系统研究。鉴定结果表明,上述10个细菌菌株分别属于埃希氏菌属(Escherichia)、金色单胞菌属(Chryseomonas)、放线杆菌属(Actinobacillus)、摩根氏菌属(Morganella)、李斯特菌属(Listeria)、金杆菌属(Aureobacterium)、微杆菌属(Microbacterium)、地杆菌属(Terrabacter)、芽孢杆菌属(Bacillus)和黄杆菌属(Flavibacterium)。     

胸窗萤的防卫行为：反射性出血及翻缩腺反应

为了探讨胸窗萤Pyrocoelia pectoralis Oliver, 1883的防卫行为, 对成虫的反射性出血行为及幼虫的翻缩腺体形态进行了研究。结果表明： 胸窗萤具有复杂的多重防卫行为策略。成虫利用闪烁、 假死、 反射性流血进行防卫, 幼虫则利用闪烁、 假死和微小的翻缩腺体进行防卫。反射性流血发生在雄成虫的前胸背板和鞘翅边缘, 而雌成虫仅在前胸背板边缘观察到有反射性流血行为。扫描电镜观察到直径大约32 μm的圆坑状结构环绕前胸背板或鞘翅边缘一圈。雌虫鞘翅牙也具有相似的圆坑状结构。幼虫具有9对乳头状的翻缩腺体, 位于中胸、 后胸和第1～7节侧板上。超薄切片发现, 腺体表面的棒状结构内部中空, 棒状结构连接一个发达的分泌细胞。细胞内连接棒状结构的部位着生致密的管状内质网。行为学实验发现, 胸窗萤血液对蚂蚁具有非常有效的拒避作用。     

The mitochondrial genome of the firefly, Pyrocoelia rufa: complete DNA sequence, genome organization, and phylogenetic analysis with other insects

The complete nucleotide sequences of the mt genome from the firefly, Pyrococelia rufa (Coeleoptera: Lampyridae) was determined. The circular genome is 17,739-bp long, and contains a typical gene complement, order, and arrangement identical to Drosophila yacuba. The presence of 1,724-bp long intergenic spacer in the P. rufa mt genome is unique. The putative initiation codon for ND1 gene appears to be TTG, instead of frequently found ATN. All tRNAs showed stable canonical clover-leaf structure of other mt tRNAs, except for tRNA(Ser) (AGN), DHU arm of which could not form stable stem-loop structure. Phylogenetic analysis among insect orders confirmed a monophyletic Endopterygota, a monophyletic Mecopterida, a monophyletic Diptera, a monophyletic Lepidoptera, and a monophyletic Coleoptera, suggesting that the complete insect mt genome sequence has a resolving power in the diversification events within Endopterygota. However, internal relationships among three coleopteran species are not clear, and the inclusion of some insect orders (i.e., apterygotan T. gertschi) in the analysis provided inconsistent results compared to other molecular studies.     

A Serine Protease Gene from the Firefly, <Emphasis Type="Italic">Pyrocoelia rufa</Emphasis>: Gene Structure,Expression, and Enzyme Activity

The gene structure, expression and enzyme activity of a serine protease from the firefly, Pyrocoelia rufa (PrSP) were examined. The PrSP gene spans 1474 bp and consists of two introns and three exons coding for 257 amino acid residues. Southern blot analysis of genomic DNA suggested the presence of PrSP gene as a single copy. Western blot analysis and enzyme activity assay exhibited midgut-specific expression, suggesting that the midgut is the prime site where large quantities of PrSP are synthesized for degrading the absorbed protein from the diet. The cDNA encoding PrSP was expressed as a 31 kDa polypeptide in the baculovirus-infected insect Sf9 cells and the recombinant PrSP showed activity in the protease enzyme assay using gelatin as a substrate.