• 제목/요약/키워드: longicorn beetle

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표고재배용(栽培用) 참나무 원목(原木)의 수종별(樹種別) 털두꺼비하늘소의 산란빈도(産卵頻度) (Differences in Ovipositional Frequency of Oak Longicorn Beetle (Moechotypa diphysis) by Oak Species Used for Lentinula edodes Cultivation Logs)

  • 구창덕;김재수;김길하;한규성;조남석;박재인;민두식
    • 한국산림과학회지
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    • 제88권4호
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    • pp.533-540
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    • 1999
  • 표고 재배용 참나무류 중에서 굴참나무는 수피가 두꺼워서 참나무의 내수피 (2차 사부조직)에 알을 낳는 털두꺼비하늘소(Moechotypa diphysis)의 산란을 어렵게 하였다. 굴참나무의 수피 두께는 평균 7.4 mm로서 다른 참나무 수종(신갈은 평균 1.1mm, 졸참은 1.3mm, 상수리는 2.0mm) 보다 3-7배나 두꺼웠다. 내수피의 두께는 상수리가 4.8mm로 가장 두껍고 다른 수종은 3.6-3.9mm 였다. 털두꺼비하늘소가 원목의 수피에 뚫은 산란공의 외부형태는 굴참나무에서 $8-12mm{\times}6-8mm$ 크기의 넓은 타원형이었으며, 다른 3수종에서는 $5-9mm{\times}1-5mm$로 좁은 타원형이었다. 털두꺼비하늘소는 굴참나무 조사목 중 9%의 원목(1.2m 길이)에 원목당 평균 3개의 산란공을 뚫었으며, 실제로 산란공에 알이 있는 비율은 15%였다. 반면에 이 하늘소가 선호하여 산란하는 수종은 신갈나무로서 조사된 원목 32개의 전부에 산란공을 뚫었으며, 원목당 산란공 수는 평균 20개, 그 산란공에 알이 있는 빈도는 56%였고, 이 중에서 35%가 6월초에 이미 부화하여 유충이 내수피를 가해하고 있었다. 털두꺼비하늘소가 산란하는데 선호하는 참나무 수종은 수피가 매끈하고 표피가 잘 벗겨지지 않는 얇은 것으로 생각된다.

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두폭, 체중 및 체장에 의한 뽕나무하늘소 유충의 성장율 비교 (The Estimate of Larval Growth of Mulberry Longicorn Beetle, Apriona germari Hope on the basis of the Larval Head Capsule Width, Larval Weight and Length)

  • 윤형주;마영일
    • 한국잠사곤충학회지
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    • 제39권2호
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    • pp.174-179
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    • 1997
  • The larval head capsule width, larval weight and length of mulberry longicorn beetle, Apriona germari Hope were measured when the larvae were exuviated in artificial diet rearing. The larval head capsule width from the 1st to the 12th instar was ranged from 0.12 to 0.69 cm, and growth ratio of each instar was significantly high between the 1st and the 2nd instars. The fitness to Dyar's law for the larval head capsule width was 87.6%. When the logarithum of the larval head capsule width is plotted against the number of instars, the calculated regression line was LogY=0.12086+0.06998X and Dyar's constant was 1.18. The larval weight was increased with larval developmental stages, and the coefficient of variation of larval weight was apparently high. But the calculated regression line was LogY=-0.91592+0.25959X and Dyar's constant was 1.25. The growth ration of the larval length was clearly high between the 2nd and the 3rd instars, and that of larvae from the 4th instar was decreased. The calculated regression line was LogY=-0.16932+0.09841X and Dyar's constant was 1.25. In conclusion, our results suggested that the larvae growth of mulberry longicorn beetle appeared to be highly related in the larval head capsule width, larval weight and length.

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A Culture-Based Study of the Bacterial Communities within the Guts of Nine Longicorn Beetle Species and their Exo-enzyme Producing Properties for Degrading Xylan and Pectin

  • Park, Doo-Sang;Oh, Hyun-Woo;Jeong, Won-Jin;Kim, Hyang-Mi;Park, Ho-Yong;Bae, Kyung-Sook
    • Journal of Microbiology
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    • 제45권5호
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    • pp.394-401
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    • 2007
  • In this study, bacterial communities within the guts of several longicorn beetles were investigated by a culture-dependent method. A total of 142 bacterial strains were isolated from nine species of longicorn beetle, including adults and larvae. A comparison of their partial 16S rRNA gene sequences showed that most of the bacteria constituting the gut communities can typically be found in soil, plants and the intestines of animals, and approximately 10% were proposed as unreported. Phylogenetic analysis demonstrated that the bacterial species comprised 7 phyla, and approximately half were Gammaproteobacteria. Actinobacteria were the second most populous group (19%), followed by Firmicutes (13%) and Alphaproteobacteria (11%). Betaproteobacteria, Flavobacteria, and Acidobacteria were minor constituents. The taxonomic compositions of the isolates were variable according to the species of longicorn beetle. Particularly, an abundance of Actinobacteria existed in Moechotypa diphysis and Mesosa hirsute, which eat broadleaf trees; however, no Actinobacteria were isolated from Corymbia rubra and Monochamus alternatus, which are needle-leaf eaters. Considerable proportions of xylanase and pectinase producing bacteria in the guts of the longicorn beetles implied that the bacteria may play an important role in the digestion of woody diets. Actinobacteria and Gammaproteobacteria were the dominant xylanase producers in the guts of the beetles.

The Effect of Cold Treatment on the Pupation and Emergence of the Mulberry Longicorn Beetle, Apriona germari Hope

  • Yoon, Hyung-Joo;Mah, Young-Il;Moon, Jae-Yu
    • International Journal of Industrial Entomology and Biomaterials
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    • 제1권2호
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    • pp.161-163
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    • 2000
  • To assess effects of cold treatment on pupation and emergence of the mulberry longicorn beetle, Apriona germari, the larvae, which ceased feeding, were exposed to three different temperature regimes (2.5, 5 and 7.5$^{\circ}C$) and preservation periods (50, 80, and l10 days). The results indicated that pupation and emergence rates of A. germari were highest at $7.5^{\circ}C$ for 110 days, 40.7% and 37.0%, respectively, demonstrating that the effect of cold treatment on metamorphosis was approximately 3 to 4 fold stronger than that of nontreatment.

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A Chymotrypsin Gene Homologue from the Mulberry Longicorn Beetle, Apriona germari: cDNA Sequence Characterization and mRNA Expression Pattern

  • Gui Zong Zheng;Lee Kwang Sik;Yoon Hyung Joo;Kim Iksoo;Sohn Hung Dae;Jin Byung Rae
    • International Journal of Industrial Entomology and Biomaterials
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    • 제11권2호
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    • pp.113-117
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    • 2005
  • A chymotrpsin gene homologue was cloned from the mulberry longicorn beetle, Apriona germari. The A. germari chymotrypsin cDNA contains an ORF of 950 nucleotides capable of encoding a 283 amino acid polypeptide with a predicted molecular mass of 29151 Da and pI of 9.38. The A. germari chymotrypsin has conserved six cysteine residues and active triad formed by His, Asp and Ser. The deduced amino acid sequence of the A. germari chymotrypsin cDNA was closest in structure to the Anthonomus grandis chymotrypsin. Northern blot analysis revealed that A. germari chymotrypsin showed the midgut-specific expression.

Effects of Rearing Temperature and Photoperiod on the Larval Development of the Mulberry Longicorn Beetle, Apriona germari Hope, on an Artificial Diet

  • Yoon, Hyung-Joo;Mah, Young-Il;Moon, Jae-Yu
    • International Journal of Industrial Entomology and Biomaterials
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    • 제1권2호
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    • pp.137-141
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    • 2000
  • To determine effects of temperatures and photoperiods on larval development of the mulberry longicorn beetle, Apriona germari, the larvae were reared at various rearing temperatures and under the various photoperiods on an artificial diet. The larval period of A. germari was extended as long as the temperature was lowered. Also the larval development in terms of length and weight of larvae was increased. However, survival rate during larval stage significantly decreased at 15$^{\circ}C$ and $20^{\circ}C$ than at $25^{\circ}C$ and $30^{\circ}C$. The results indicated that the favorable temperature for artificial diet rearing of A. germari fell at least above $25^{\circ}C$ constantly. In photoperiod conditions, survival rate and larval development for A. germari were obviously most effective under a photoperiod of 14L:10B. As a result in artificial diet rearing of a. germari at $25^{\circ}C$ and under a photoperiod of 14L:10D was mostly favorable in terms of larval development and period.

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Molecular Cloning of a LIM Protein cDNA from the Mulberry Longicorn Beetle, Apriona germari

  • Gui, Zhongzheng;Wei, Yadong;Yoon, Hyung Joo;Kim, Iksoo;Guo, Xijie;Jin, Byung Rae;Sohn, Hung Dae
    • International Journal of Industrial Entomology and Biomaterials
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    • 제9권1호
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    • pp.149-153
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    • 2004
  • Here we report the molecular cloning of a LIM protein cDNA of the CRP (cysteine-rich protein) family from the mulberry longicorn beetle, Apriona, geramri. The A. germari LIM protein cDNA contains an open reading frame of 276 bp encoding 92 amino acid residues with a calculated molecular weight of approximately 10 kDa. The A. germari LIM protein contains the cysteine-rich consensus sequence of LIM domain and the glycine-rich consensus sequence observed in cysteine-rich protein family 1 (CRP1). The potential nuclear targeting signal is retained. The deduced amino acid sequence of the A. germari LIM protein cDNA showed 81 % identity to both Bombyx mori muscle LIM protein (Mlp) and Drosophila melanogaster Mlp60A and 77% to Epiblema scudderiana Mlp. Northern blot analysis showed that A. germari LIM protein is highly expressed in epidermis and muscle, and less strongly in midgut, but not in the fat body.

뽕나무 하늘소(Apriona germari Hope)로부터 Beauveria속 사상균의 분리 및 PCR에 의한 동정 (Identification of Beauveria spp. Isolated from Mulberry Longicorn Beetle (Apriona germari Hope) using Polymerase Chain Reaction)

  • 서종복;진병래
    • 한국잠사곤충학회지
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    • 제37권2호
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    • pp.167-171
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    • 1995
  • 딱정벌레목 천공성 해충인 뽕나무 하늘소(Apriona germari)의 효과적인 방제를 위하여, 뽕나무 하늘소 이병충으로 부터 곤충병원 사상균을 분리하고, 위상차 현미경 및 주사전자현미경으로 관찰하였으며, PCR(polymerase chain reaction)을 이용하여 동정하였다. 뽕나무 하늘소 이병충으로 부터 분리된 곤충병원 사상균은 현미경 관찰 결과 Beauveria속의 전형적인 형태적 특성을 나타냈다. 따라서 이들의 용이한 동정을 위하여 PCR primer(5'-ACG GGC GCT C-3')를 이용한 RAPD(random amplification of polymorphic DNA) 방법으로 분석하고, B. bassiana와 B. brongniartii의 PCR 산물을 전기영동한 결과 DNA 표식자로 이용이 가능하였다. 이상의 결과로서 본 실험에서 분리·명명된 SFB-1A는 B. bassianifh, SFB-1A는 B. bassiana로, SFB-3A는 B. brongniartii로 동정되었다.

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Molecular Cloning of a cDNA Encoding a Cathepsin B Homologue from the Mulberry Longicorn Beetle, Apriona germari

  • Kim, Seong-Ryul;Yoon, Hyung-Joo;Park, Nam-Sook;Lee, Sang-Mong;Moon, Jae-Yu;Jin, Byung-Rae;Sohn, Hung-Dae
    • International Journal of Industrial Entomology and Biomaterials
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    • 제4권1호
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    • pp.63-68
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    • 2002
  • A cDNA encoding a putative member of cathepsin B of the thiol pretense superfamily was cloned from a cDNA library of the mulberry longicorn beetle, Apriona germari. Sequence analysis of the cDNA encoding the cathepsin B of A. germari (AgCatB) revealed that the 972 bp cDNA has an open reading frame of 324 amino acid residues. The deduced protein sequence of the AgCatB showed high homology with cathepsin B of the insects, Bombyx mori (47.3% amino acid identity), Helicoverpa armigera (46.6%) and Sarcophaga peregrina (45.6%), and the lowest homology with Aedes aegypti (33.2%). The AgCatB contains six disulfate bonds typical for cysteine pretenses. The three amino acid positions Cys-109, His-267, and Asn-287 which are conserved, active sites characteristic for cathepsin B, were also found. Phylogenetic analysis further confirmed that the AgCatB has a close relationship with that of B. mori, H. armigera and S. peregrina.

Cloning and Gene Manipulation of a cDNA Encoding A Cellulase Produced by the Mulberry Longicorn Beetle, Apriona germari

  • Kim, Yong-Soon;Lee, Sung-Jin;Sohn, Bong-Hee;Kang, Pil-Don;Lee, Sang-Uk;Jin, Byung-Rae
    • 한국잠사학회:학술대회논문집
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    • 한국잠사학회 2003년도 International Symposium of Silkworm/Insect Biotechnology and Annual Meeting of Korea Society of Sericultural Science
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    • pp.157-159
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    • 2003
  • We have cloned and sequenced the cDNA coding fur a cellulase from the mulberry longicorn beetle, Apriona germari, with the polymerase chain reaction. And then we have constructed the recombinant plasmid vector for Bombyx mori transfomation experiment. (omitted)

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