菜蚜茧蜂载体植物系统的构建及其控害效果

载体植物系统是近年发展的新型生物防治技术。本文以桃蚜Myzus persicae Sulzer、甘蓝蚜Brevicoryne brassicae(Linnaeus)和蚕豆蚜Aphis craccivora为候选替代寄主,烟草、玉米、生菜、甘蓝、蚕豆和菜薹为候选载体植物,确定了菜蚜茧蜂的替代寄主为桃蚜,载体植物为烟草。在确定了合适的蜂(♀)蚜比(1∶100)后,以起始桃蚜量2000头/株构建了载体植物系统。该系统28 d内共产生2770头僵蚜,羽化率为83.33%。在菜蚜为100头的菜薹上接入1头由载体植物系统繁殖所得的雌性菜蚜茧蜂,任其自由寄生24 h后移出,其对目标害虫菜蚜的寄生率达到71.17%。在温室1 m×1 m×1 m的白色网笼中放置菜薹植株15盆,分别向每株菜薹上接入菜蚜20头,自由繁殖15 d后置入1株菜蚜茧蜂载体植物系统,其后7 d和14 d的菜蚜减退率分别为83.11%和95.80%。这说明菜蚜茧蜂载体植物系统能产生大量菜蚜茧蜂,并且在温室中能成功地控制菜蚜危害。     

田间不同品种蔬菜对萝卜蚜种群的影响(英文)

本试验通过利用５个品种蔬菜（萝卜,芥蓝,芥菜,菜芯和白菜）研究萝卜蚜（Ｌｉｐａｐｈｉｓ ｅｒｙｓｉｍｉ）在不同蔬菜上的种群动态以及对寄生于萝卜蚜的菜蚜茧蜂（Ｄｉａｅｒｅｔｉｅｌｌａ　ｒａｐａｅ）种群的影响。研究结果显示,在３０天研究期间,有翅萝卜蚜的平均虫口（蚜虫数／苗）在萝卜、芥蓝、芥菜、菜芯和白菜苗上分别为３．９１８、０．８３１、１．１４９、１．７４３和５．２３头,表明降落在萝卜苗上的有翅蚜数量显著地比在其它蔬菜苗上的高;而无翅萝卜蚜的中均虫口分别为６３．４２１、１０．０４１、２４．９２８、２３．３２３和１１４．３０８头,说明萝卜蚜无翅蚜在白菜上的种群显著地高于其它品种蔬菜上的。由于萝卜蚜在不同品种蔬菜上的种群不同,导致菜蚜茧峰种群在不同品种蔬菜上也不同,其僵蚜虫口分别为１．０５６、０．２５１、０．２７７、０．６５１和１．４４头,显示了在萝卜和白菜上的僵蚜数量显著地比其它蔬菜上的高。分析结果表明,萝卜蚜的种群（ｘ）与菜蚜茧峰的种群（ｙ）呈显著的相关关系：ｙ＝０．１１８８＋０．０１４３ｘ（ｒ＝０．９７３９）。本研究还利用试验结果提出了萝卜蚜无翅蚜种群从蔬菜在田间种植后达到防治指标（５０头／苗）的临界天数（ｃ     

麦双尾蚜及其天敌在春小麦和野生寄主上的种群动态

在塔城麦田调查发现,麦双尾蚜Diuraphis noxia (Mordvilko) 在春小麦和野生寄主上的百株蚜量从大到小依次为春小麦、黑麦和野燕麦,在春小麦上最早出现高峰期。在春小麦上,瓢虫类数量最多达到516头/百株,菜蚜茧蜂Diaeretiella rapae和白足蚜小蜂Aphelinus albipodus的最高寄生率分别达到31.6%和12.9%。在黑麦上,麦双尾蚜主要被白足蚜小蜂寄生,最高寄生率达到42.9%,斑腹蝇幼虫Leucopis annulipes最高达到16头/百株。在野燕麦上,白足蚜小蜂和菜蚜茧蜂最高寄生率分别达到62.3%和31.8%。瓢虫和菜蚜茧蜂发生较早,白足蚜小蜂和斑腹蝇发生时间相对较晚。     

烟蚜茧蜂随寄主有翅桃蚜迁飞而被携带扩散的模拟实验

蚜虫寄生蜂的广泛分布可能与有翅蚜的迁飞有关。为了证明这一假说, 本研究利用微小昆虫飞行磨系统, 分数十批(≤16头/批)对被烟蚜茧蜂Aphidius gifuensis Ashmead单头寄生后的有翅桃蚜Myzus persicae (Sulzer)进行模拟飞行并系统观察了飞行后有翅桃蚜的单头定殖情况。对实验观察数据按飞行时间和飞行距离进行归类, 采用单因素方差分析方法分析飞行时间和飞行距离对有翅桃蚜定殖后的存活和生殖力、烟蚜茧蜂发育等变量的影响; 采用多项式回归分析对所有变量和归类的数据进行统计和分析。结果表明: 成功飞行并定殖的有翅桃蚜有378头, 其中239头有翅桃蚜定殖后形成僵蚜。形成僵蚜的有翅桃蚜在飞行实验时平均飞行时间和飞行距离分别为2.63 h和2.16 km, 定殖后平均存活了6.11 d, 定殖第6天和第14天平均产若蚜累计数量分别为8.5头和162头。形成僵蚜和未形成僵蚜的有翅蚜的模拟飞行数据和定殖观察数据无显著差异。形成僵蚜的239头有翅桃蚜中, 最终成功育出烟蚜茧蜂205头, 僵蚜出蜂率为85.8%。雌雄性比为1∶5.2。结论认为, 专性寄生蚜虫的烟蚜茧蜂可以利用有翅蚜的迁飞而被携带扩散传播, 有翅蚜迁飞在蚜虫寄生蜂扩散中具有重要作用。     

球孢白僵菌对烟蚜茧蜂生命参数及控害效果的影响

在室内评价了球孢白僵菌对烟蚜茧蜂生命参数及控害效果的影响。分别在烟蚜茧蜂寄生桃蚜后不同时间进行高剂量（1900孢子/mm^{2）接菌,检测蚜虫感病率和寄生蜂形成的僵蚜率及僵蚜出蜂率。结果表明,球孢白僵菌对僵蚜率和僵蚜出蜂率的影响随接菌时间不同而变化。在烟蚜茧蜂寄生前1d、寄生当天和寄生后3d接菌,蚜虫感病率分别为59.6%、56.2%和34.8%;与对照相比,僵蚜率分别下降94%、59%和47%,僵蚜出蜂率分别减少83%、54%和49%。在寄生后5d或7d接菌,僵蚜率和僵蚜出蜂率不受明显影响,但蚜虫感病率降低到8.2%以下。对蚜尸内白僵菌菌体含量检测表明,随着烟蚜茧蜂寄生后接菌时间的推移,菌体数量迅速下降。寄生蜂寄生后5d或7d接菌,蚜尸内几乎检测不到菌体。直接喷雾接菌烟蚜茧蜂,成蜂寿命缩短4d左右,且81.8%的蜂尸受白僵菌感染。接菌后的寄生蜂对蚜虫寄生率几乎无影响,但寄生蜂在蚜虫体内的存活时间缩短了27.8%。}     

球孢白僵菌对烟蚜茧蜂生命参数及控害效果的影响

在室内评价了球孢白僵菌对烟蚜茧蜂生命参数及控害效果的影响。分别在烟蚜茧蜂寄生桃蚜后不同时间进行高剂量(1900孢子/mm2)接菌,检测蚜虫感病率和寄生蜂形成的僵蚜率及僵蚜出蜂率。结果表明,球孢白僵菌对僵蚜率和僵蚜出蜂率的影响随接菌时间不同而变化。在烟蚜茧蜂寄生前1d、寄生当天和寄生后3d接菌,蚜虫感病率分别为59.6%、56.2%和34.8%;与对照相比,僵蚜率分别下降94%、59%和47%,僵蚜出蜂率分别减少83%、54%和49%。在寄生后5d或7d接菌,僵蚜率和僵蚜出蜂率不受明显影响,但蚜虫感病率降低到8.2%以下。对蚜尸内白僵菌菌体含量检测表明,随着烟蚜茧蜂寄生后接菌时间的推移,菌体数量迅速下降。寄生蜂寄生后5d或7d接菌,蚜尸内几乎检测不到菌体。直接喷雾接菌烟蚜茧蜂,成蜂寿命缩短4d左右,且81.8%的蜂尸受白僵菌感染。接菌后的寄生蜂对蚜虫寄生率几乎无影响,但寄生蜂在蚜虫体内的存活时间缩短了27.8%。     

烟草品种、育苗方式和烟蚜来源对烟蚜茧蜂寄生能力的影响

【目的】本研究旨在筛选出适合烟蚜茧蜂Aphidius gifuensis寄生烟蚜Myzus persicae的烟草品种、育苗方式和烟蚜来源,为烟蚜茧蜂人工繁殖和复壮提供科学参考。【方法】采用盆栽法,调查了不同烟草品种(云烟87、K326、翠碧1号和红花大金元)繁殖烟蚜若蚜、不同来源烟蚜(来自烟区、来自非烟区和室内繁殖种群)若蚜和烟草不同育苗方式(土壤育苗和湿润育苗)繁殖烟蚜若蚜时,烟蚜茧蜂成蜂对烟蚜若蚜的寄生率以及成蜂羽化率、寿命、体型大小和雌蜂比。【结果】结果表明,不同烟草品种繁殖烟蚜若蚜对烟蚜茧蜂成蜂寄生率存在显著影响。其中,在红花大金元和翠碧1号繁殖烟蚜上的烟蚜茧蜂成蜂寄生率分别比在K326繁殖烟蚜上的烟蚜茧蜂成蜂寄生率高19.00%和14.00%,但对烟蚜茧蜂的其他指标没有显著影响;不同烟蚜来源对烟蚜茧蜂寄生率也存在显著影响,其中,烟蚜茧蜂成蜂对非烟区烟蚜若蚜和烟区烟蚜若蚜的寄生率比对室内繁殖种群烟蚜若蚜的寄生率分别高20.25%和16.75%,但对烟蚜茧蜂成蜂的羽化率、寿命、体型大小和雌蜂比没有显著影响;烟草不同育苗方式对烟蚜茧蜂成蜂的寄生率无显著影响。【结论】烟蚜茧蜂对烟蚜...     

烟蚜茧蜂寄生对烟蚜生长发育和繁殖的影响

【目的】为探究烟蚜茧蜂Aphidius gifuensis对烟蚜Myzus persicae寄生后烟蚜生长发育和繁殖影响及其在烟蚜防控中的作用。【方法】采用室内叶片培养皿法,测定了不同龄期烟蚜(1-4龄若蚜及成蚜)被烟蚜茧蜂寄生后烟蚜当代(F₀)及后代(F₁)的发育历期、寿命、产仔量。【结果】烟蚜1龄若蚜被烟蚜茧蜂寄生后,1龄若蚜历期受到显著影响,较未被寄生对照缩短了0.65 d (33.00%),而2-4龄若蚜期和成蚜历期未受显著影响;2龄若蚜被寄生后,4龄若蚜和成蚜历期均受到显著影响,较未被寄生的对照分别缩短了1.50 d (100.00%)和0.83 d (100.00%),而2和3龄若蚜期未受显著影响;3龄若蚜被寄生后,4龄若蚜和成蚜期均受到显著影响,较未被寄生对照分别缩短了1.50 d (100.00%)和0.83 d (100.00%),而3龄若蚜期未受显著影响。2龄若蚜被寄生后烟蚜的寿命和产仔量均受到显著影响,寿命较未被寄生对照缩短了8.39 d(54.00%),每雌产仔量较未被寄生对照减少了48.67头(100.00%)。此外,2-3龄若蚜被寄生后其后代(F₁)1龄若蚜历期受影响最大,较未被寄生烟蚜后代1龄若蚜期缩短了0.80 d(40.00%),其F₁代平均寿命较未被寄生烟蚜后代平均寿命延长了5.72 d(41.20%),但其产仔量与对照差异不显著。【结论】不同龄期烟蚜被烟蚜茧蜂寄生后,其发育历期和寿命比未被寄生的缩短,产仔量比被未寄生的少,但其F₁代平均寿命比未被寄生后代烟蚜的长且其产仔量未受显著影响。当代2龄若蚜期是控制烟蚜增长的关键时期。这些结果对确定烟蚜茧蜂防治烟蚜适期及认识其机理具有重要参考意义。     

桃蚜被寄生龄期与受寄生蜂影响大小的关系

在两个温度下将桃蚜Myzus perstcae无翅型不同龄期个体供菜蚜茧蜂Diaeretiella rapae产卵寄生,然后观察寄主蚜虫的发育、存活和生殖情况.结果表明,寄主蚜虫的发育速率不受影响,而从接受寄生蜂产卵到生殖率明显下降、产幼蚜终止、死亡三种症状出现的时间间隔分别为寄生蜂完成整个幼期发育所需时间的30%、40%、60%左右,这一规律不依寄主接受产卵的龄期和温度条件而变化,从而导致寄主所受影响随着接受产卵时龄期的增大而迅速下降.当蚜虫在1—2龄接受产卵时,一般不能产幼蚜,从二龄后期起,随着接受产卵龄期的推迟,所表现的内禀增长能力迅速增加,至羽化为成蚜时接受产卵,内禀增长能力已与未被寄生蚜虫的接近.由此可见,寄主不同龄期被产卵寄生的相对机率是影响蚜虫-蚜茧蜂混合种群动态关系的决定性因子之一,蚜茧蜂必须产卵于大量的1—3龄若蚜,才有可能对蚜虫种群的增长有明显的抑制作用.     

日本柄瘤蚜茧蜂与其寄主豆蚜的相互作用：寄主龄期选择及其对发育的影响

在25℃下研究了日本柄瘤蚜茧蜂Lysiphlebus japonicus Ashmead对寄主豆蚜Aphis craccivora Koch龄期的选择和被寄生豆蚜的龄期对蚜茧蜂发育的影响。结果表明：在混合虫态寄主中,日本柄瘤蚜茧蜂通常选择较小龄期的若蚜寄生,其中2龄若蚜的相对被寄生率最高,为26.4%;其次是1龄若蚜,为20.6%;无翅成蚜与3、4龄有翅若蚜和成蚜的相对被寄生率较低。日本柄瘤蚜茧蜂的寄生延长了豆蚜若蚜的发育,其中1龄若蚜被寄生后,１～３龄历期显著延长;有翅3龄若蚜被寄生后,３、４龄历期明显延长;但无翅和有翅4龄若蚜被寄生后的发育历期均不受影响。各龄若蚜被寄生后羽化的成蚜寿命明显缩短,其中,被寄生的1龄若蚜不能发育至成蚜,其它较早龄期被寄生的若蚜羽化的成蚜繁殖力均显著降低。寄生时寄主的发育期也影响寄生蜂的发育,2龄豆蚜被寄生时的日本柄瘤蚜茧蜂个体发育最快,为194.10 h;1龄寄主被寄生时蚜茧蜂的发育最慢,需215.80 h。并对不同发育期蚜虫总蛋白质和总糖原含量进行了测定。     

Collagen-like triple helix formation of synthetic (Pro-Pro-Gly)10 analogues: (4(S)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10, (4(R)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10 and (4(S)-fluoroprolyl-4(R)-fluoroprolyl-Gly)10.

For the rational design of a stable collagen triple helix according to the conventional rule that the pyrrolidine puckerings of Pro, 4-hydroxyproline (Hyp) and 4-fluoroproline (fPro) should be down at the X-position and up at the Y-position in the X-Y-Gly repeated sequence for enhancing the triple helix propensities of collagen model peptides, a series of peptides were prepared in which X- and Y-positions were altogether occupied by Hyp(R), Hyp(S), fPro(R) or fPro(S). Contrary to our presumption that inducing the X-Y residues to adopt a down-up conformation would result in an increase in the thermal stability of peptides, the triple helices of (Hyp(S)-Hyp(R)-Gly)(10) and (fPro(S)-fPro(R)-Gly)(10) were less stable than those of (Pro-Hyp(R)-Gly)(10) and (Pro-fPro(R)-Gly)(10), respectively. As reported by B?chinger's and Zagari's groups, (Hyp(R)-Hyp(R)-Gly)(10) which could have an up-up conformation unfavorable for the triple helix, formed a triple helix that has a high thermal stability close to that of (Pro-Hyp(R)-Gly)(10). These results clearly show that the empirical rule based on the conformational preference of pyrrolidine ring at each of X and Y residues should not be regarded as still valid, at least for predicting the stability of collagen models in which both X and Y residues have electronegative groups at the 4-position.     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

Role of tfdC(I)D(I)E(I)F(I) and tfdD(II)C(II)E(II)F(II) gene modules in catabolism of 3-chlorobenzoate by Ralstonia eutropha JMP134(pJP4)

The enzymes chlorocatechol-1,2-dioxygenase, chloromuconate cycloisomerase, dienelactone hydrolase, and maleylacetate reductase allow Ralstonia eutropha JMP134(pJP4) to degrade chlorocatechols formed during growth in 2,4-dichlorophenoxyacetate or 3-chlorobenzoate (3-CB). There are two gene modules located in plasmid pJP4, tfdC(I)D(I)E(I)F(I) (module I) and tfdD(II)C(II)E(II)F(II) (module II), putatively encoding these enzymes. To assess the role of both tfd modules in the degradation of chloroaromatics, each module was cloned into the medium-copy-number plasmid vector pBBR1MCS-2 under the control of the tfdR regulatory gene. These constructs were introduced into R. eutropha JMP222 (a JMP134 derivative lacking pJP4) and Pseudomonas putida KT2442, two strains able to transform 3-CB into chlorocatechols. Specific activities in cell extracts of chlorocatechol-1,2-dioxygenase (tfdC), chloromuconate cycloisomerase (tfdD), and dienelactone hydrolase (tfdE) were 2 to 50 times higher for microorganisms containing module I compared to those containing module II. In contrast, a significantly (50-fold) higher activity of maleylacetate reductase (tfdF) was observed in cell extracts of microorganisms containing module II compared to module I. The R. eutropha JMP222 derivative containing tfdR-tfdC(I)D(I)E(I)F(I) grew four times faster in liquid cultures with 3-CB as a sole carbon and energy source than in cultures containing tfdR-tfdD(II)C(II)E(II)F(II). In the case of P. putida KT2442, only the derivative containing module I was able to grow in liquid cultures of 3-CB. These results indicate that efficient degradation of 3-CB by R. eutropha JMP134(pJP4) requires the two tfd modules such that TfdCDE is likely supplied primarily by module I, while TfdF is likely supplied by module II.     

Induction of in vitro flowering in Dendrobium Madame Thong-In (Orchidaceae) seedlings is associated with increase in endogenous N(6)-(Delta (2)-isopentenyl)-adenine (iP) and N (6)-(Delta (2)-isopentenyl)-adenosine (iPA) levels

We analysed the endogenous cytokinin levels of Dendrobium Madame Thong-In seedlings grown in vitro during vegetative and flowering-inductive periods. HPLC was used to fractionate the extracts and radioimmunoassay (RIA) was used for assay of zeatin (Z), dihydrozeatin (DZ), N(6)-(Delta(2)-isopentenyl)-adenine (iP) and their derivatives. Coconut water used in experiments was found to contain high level (>136 pmol ml(-1)) of zeatin riboside (ZR). Protocorms and seedlings cultured in medium with coconut water were found to contain 0.5-3.9 pmol g(-1) FW of the cytokinins analysed. Seedlings (1.0-1.5 cm) cultured in flowering-inductive liquid medium containing 6-benzyladenine (BA, 4.4 muM) and coconut water (CW, 15%) contained up to 200 and 133 pmol g(-1) FW of iP and iPA, respectively. These levels were significantly higher than all other cytokinins analysed in seedlings of the same stage and were about 80- to 150-folds higher than seedlings cultured in non-inductive medium. During the transitional (vegetative to reproductive) stage, the endogenous levels of iP (178 pmol g(-1) FW) and iPA (63 pmol g(-1) FW) were also significantly higher than cytokinins in the zeatine (Z) and dihydrozeatin (DZ) families in the same seedlings. Seedlings that grew on inductive medium but remained vegetative contained lower levels of iPA. The importance of the profiles of iP and its derivatives in induction of in vitro flowering of D. Madame Thong-In is discussed.     

Biology of Bactrocera (Zeugodacus) tau (Walker) (Diptera: Tephritidae)

The biology of the fruit fly Bactrocera tau, an important horticultural pest, was studied under laboratory conditions at 25°C and 60–70% relative humidity on Cucurbita maxima. The duration of mating averaged 408.03 ± 235.93 min. After mating, the female fly had a preoviposition period of 11.7 ± 4.49 days. The oviposition rate was 9.9 ± 8.50 eggs and fecundity was 464.6 ± 67.98 eggs/female. Eggs were elliptical, smooth and shiny white, turning darker as hatching approached, and measured 1.30 ± 0.07 mm × 0.24 ± 0.04 mm. The chorion has polygonal microsculpturing and is species-specific with polygonal walls. The egg period lasts for 1.3 ± 0.41 days. The duration of the larval period is 1.2 ± 0.42, 1.7 ± 0.48 and 4.0 ± 0.94 days for first, second and third instars, respectively. Pupation occurs in the sand or soil and pupal periods are 7.0 ± 0.47 days. The life cycle from egg to adult was completed in 14.2 ± 1.69 days; the longevity of mated females and males was 130.33 ± 14.18 and 104.66 ± 31.21 days, respectively. At least two to three generations were observed from June 2008 to June 2009.     

Spectroscopic investigations of Er(3+) :CdO-Bi(2) O(3) -B(2) O(3) glasses

This article reports on the optical properties of Er³⁺ ions doped CdO–Bi₂O₃–B₂O₃ (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ω_λ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er³⁺:CdBiB glasses. The concentration quenching and energy transfer from Yb³⁺–Er³⁺ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er³⁺:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd.     

Cationic (tripyrrinato)palladium(II) complexes

The formation of cationic palladium(II)complexes [TrpyPd^II]⁺X⁻ by salt metathesis of the respective trifluoroacetates with different salts of weakly coordinating anions X⁻ was investigated. With non-hydrolizable counterions, cationic mono- and dinuclear complexes are observed depending on the nature of the anion X⁻ and the solvent. The mononuclear cations, which are only formed with X = BAr^F, most probably carry a weakly bound molecule of dichloromethane at the fourth coordination site of Pd^II. When treated with diazoalkanes, only these are sufficiently reactive to form carbene complexes. Four- and five coordinate Lewis base adducts [TrpyPd^IIL]⁺ with L = CH₃NC, tBuNH₂, PMe₃, PEt₃ and PiPr₃ and [TrpyPd^IIL₂]⁺ with L = PMe₃ were prepared from the mononuclear cations [TrpyPd^II]⁺BAr^F−. From structural studies it becomes apparent, that the formation of stable five coordinate Pd^II species is restricted to medium size ligands and depends on the delicate balance between the steric influence of L and the strain, which is induced on the TrpyPd^II unit.     

The helix-coil transitions of poly (dA)-poly (dT) and poly (dA-dT)-poly (dA-dT)

Helix–coil transition curves are calculated for poly (dA) poly(dT) and poly (dA-dT) poly (dA-dT) using the integral equation approach of Goel and Montroll.⁵ The transitions are described by the loop entropy model with the exponent of the loop entropy factor, k, remaining an arbitrary constant. The theoretical calculations are compared with experimental transition curves of the two polymers. Results indicate that the stacking energies for these two polymers differ by about 1 kcal/mole of base pairs. Also, a fit between theory and experiment was not possible for k > 1.70.