Anomalous couplings of non-BPS D-branes

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谷子非特异性磷脂酶C基因SiNPC4的克隆及功能分析

谷子非特异性磷脂酶C基因SiNPC4的克隆及功能分析

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作物学报
第 41 卷
Arabidopsis carrying SiNPC4 decreased the sensitivity to ABA and BL compared with WT. Thus, we deduced that SiNPC4 may act as a negative regulator in ABA and BL signaling pathways. Besides, there were no significant difference in growth between transgenic and wild type plants under drought and high salinity treatments. Keywords: Foxtail millet; SiNPC4; Abiotic stress; ABA; BL
磷脂酶是一类磷脂水解酶, 根据水解磷脂位点 的不同主要分为3个家族(磷脂酶A、磷脂酶C和磷脂 酶D)[1], 在响应植物生物和非生物胁迫信号转导途 径中发挥重要作用[2-4]。其中, 磷脂酶C (PLC)依水解 底物不同分为特异性水解磷脂酰肌醇磷脂酶C (PI-PLC)和非特异性磷脂酶C (NPC)[5]。NPC类磷脂 酶 是 在 植 物 中 发 现 的 与 细 菌 PC-PLC 同 源 的 新 型 磷 脂酶[6-7], 拟南芥和水稻中分别有6个和5个NPC类磷 脂酶基因[6,8]。研究表明, NPC类基因在不同处理条 件下的表达模式不同, 分别参与不同生长发育和逆 境响应过程。在拟南芥中, AtNPC1在各个器官的表 达 量 相 当 , AtNPC2 和 AtNPC6 在 角 果 中 表 达 最 高 , AtNPC3主要在根部表达, AtNPC4主要在成熟的叶片 和根部表达, AtNPC5主要在花序中表达。AtNPC4对 ABA信号途径起正向调控作用[7], 在拟南芥中过表 达AtNPC4植物对干旱和高盐胁迫的抗性增强[7,9]。 AtNPC3和AtNPC4受低磷胁迫诱导表达, 并且参与 生 长 素 (IAA) 和 油 菜 素 内 酯 (BL) 介 导 的 根 系 生 长 发 育过程[6,10]。 AtNPC5在低盐胁迫下表达显著上调, 促进侧根生长[11]。在水稻中, OsNPC1在盐胁迫条件 下 表 达 上 升 , 低 温 条 件 下 表 达 下 降 ; OsNPC2 和 OsNPC4均受盐和干旱诱导表达; OsNPC5受低温和 干旱诱导表达下调; OsNPC3表达不受干旱、低温和 高盐胁迫的影响; OsNPC2、OsNPC4和OsNPC5在生 殖发育阶段表达上调; 在种子发育的晚期, 只有 OsNPC4 表 达 持 续 增 加 ; 圆 锥 花 序 阶 段 , 只 有 OsNPC1表达下调。此外, NPC类蛋白的亚细胞定位 也不相同, AtNPC5定位在胞质[12], AtNPC4定位在质 膜上[6], OsNPC1主要定位在细胞质, OsNPC3定位在 叶绿体中[8]。

遗传学名词解释大全

遗传学名词解释大全

autoregulation 自我调节:基因通过自身的产物来调节转录。

autosome 常染色体:性染色体以外的任何染色体。

auxotroph 营养缺陷型:微生物的一种突变体,它不能合成生长所需的物质,培养时必须在培养基中加入此物质才能生长。

back mutation 回复突变:见reversionbacteriophage (phage) 一种感染细菌的病毒。

balance model 平衡模型:关于遗传变异比例的一种模型,它认为自然选择维持了群体中大量遗传变异的存在。

balanced polymorphism 平衡多态现象:稳定的遗传多态现象是由自然选择来维持的。

Barr body 巴氏小体:在正常雌性哺乳动物的核中有一个高度凝聚的染色质团,它是一个失活的X染色体。

base analog 碱基类似物:一种化学物质,其分子结构和DNA的碱基相似,在DNA的代谢过程中有时会取代正常碱基,结果使DNA的碱基发生突变。

bead theory 串珠学说:已被否定的学说,认为基因附着在染色体上,就象项链上的串珠。

它既是突变单位又是重组单位。

binary fission 二分分裂:一个细胞分裂为大小相近的两个子细胞的过程。

binomial distribution 二项分布:具有两种可能结果的biparental zygote 双亲合子:又称双亲遗传(biparental inheriance),衣藻(chlamydomonas)的合子含有来自双亲的DNA。

这种细胞一般很少见。

biochemical mutation 生化突变,见自发突变(autotrophic mutation)。

bivalent 二价体:在第一次减数分裂时彼此联合的一对同源染色体。

bottleneck effect 瓶颈效应:一种类型的漂变。

当群体很小时产生这种效应,结果使基因座中有的基因丢失了。

branch-point sequence 分支点顺序:在哺乳动物细胞中的保守顺序:YNCURAY(Y: 嘧啶,R:嘌呤, N:任何碱基),位于核mRNA内含子和II 类内含子3'端附近,其中的A可通过5'-2'连接的方式和内含子5'端相连接,在剪接时形成套马索状结构。

211001976_沙门菌SptP调控巨噬细胞MAPK-CDK6-RB通路的初步分析

211001976_沙门菌SptP调控巨噬细胞MAPK-CDK6-RB通路的初步分析
Abstract:ThepurposeofthisstudywastoexploretheeffectofSalmonellavirulencefactorSptP on MAPK-CDK6-RB pathwayandtheformationof macrophageextracellulartraps (METs). Firstly,comparethe difference of METslevelsinduced by Salmonella 13312 (Salmonella Choleraesuis),Salmonella14028 (Salmonella Typhimurium)andSalmonella13314 (Salmonella Arizona).Then,predicttheSalmonellagenesinvolvedintheregulationofMETsusingbioinformaticsmethod.Finally,verifytheresultusingChIPand MALDI-TOFexperiments.Theresults showedthatthelevelsofMETsinducedbySalmonella13312andSalmonella14028weresignificantlylowerthanSalmonella13314 (P<0.05),suggestedthatSalmonellagenesmayregulate somekeystepsofthebiogenesisofMETsthroughacertainpathway.ThebioinformaticspredictionofDomain—DomaininteractioncombinedwithChIPand MALDI-TOFexperimentsshowed thattheSalmonellageneSptPparticipatedinthisprocess,anditshosttargetmoleculesmaybe

鲍曼不动杆菌专家共识解读

鲍曼不动杆菌专家共识解读
• 鲍曼不动杆菌感染的抗菌治疗原则 • 治疗鲍曼不动杆菌感染的常用抗菌药物 • 不动杆菌感染的抗菌药物选择 • 联合抗菌治疗
共识主要内容(2)
✓ 主要感染类型与诊治 • 肺炎 • 血流感染 • 颅内感染 • 腹腔感染 • 泌尿系感染 • 皮肤软组织感染 • 其他
共识主要内容(3)
✓ 鲍曼不动杆菌感染防控 • 加强抗菌药物临床管理 • 阻断鲍曼不动杆菌的传播途径
220 (3.9)
191 (3.4、 86.8)
180 (7.2)
168 (6.7、 93.3)
180 (7.2)
168 (、 93.3)
5523(11.5)
4949 (10.3、 87.8)
国内外对鲍曼不动杆菌的关注度迅速 增加
PUBMED近10年发表的关于鲍曼不动 杆菌的学术文献数量为2069篇,其中
• 2、药物作用靶位改变:拓扑异构酶gyrA、 parC基因突变导致的喹诺 酮类药物耐药,armA等16S rRNA甲基化酶导致所有氨基糖苷类抗生素 耐药;
• 3、药物到达作用靶位量的减少:包括外膜孔蛋白通透性的下降及外排 泵的过度表达。鲍曼不动杆菌基因组显示[13],其富含外排泵基因,外 排泵高表达在鲍曼不动杆菌多重耐药中发挥重要作用。
人体传染源
患者定植 •皮肤 •咽喉 •腋窝 •腹股沟 •会阴部 •消化道 感染患者 •肺炎、支气管炎 •血流感染 •尿路感染 •中枢神经系统感染 •腹膜炎 •皮肤和软组织感染 健康护理工作者 •经手传染
非生命体传染源
医疗器械 •呼吸机 •听诊器 •监护仪 •静脉泵 •支气管镜 •血压表套袖等 医院环境 •床垫、床头框架 •枕头 •窗帘 •洗涤槽 •垃圾桶 •电脑键盘等
• 含舒巴坦的合剂(如氨苄西林/舒 巴坦、头孢哌酮/舒巴坦)可用于 鲍曼不动杆菌感染的治疗

非富勒烯小分子受体不稳定单元

非富勒烯小分子受体不稳定单元

非富勒烯小分子受体不稳定单元英文回答:Non-fullerene small molecule acceptors (NF-SMAs) have attracted considerable attention as promising alternatives to fullerenes in organic solar cells (OSCs) due to their tunable optoelectronic properties, ease of synthesis, and low cost. However, the instability of NF-SMAs under ambient conditions remains a major challenge that hinders their practical application. The instability of NF-SMAs is primarily attributed to the presence of labile chemical bonds, such as C-C and C-H bonds, which are susceptible to attack by oxygen and moisture.Several strategies have been developed to improve the stability of NF-SMAs. One approach involves theintroduction of bulky side chains or steric hindrance around the labile bonds. This approach can effectively reduce the accessibility of these bonds to oxygen and moisture, thereby enhancing the stability of the NF-SMAs.Another approach involves the use of cross-linking agents to form covalent bonds between the NF-SMAs and the polymer matrix. This approach can prevent the NF-SMAs fromdiffusing out of the active layer and improve the long-term stability of the OSCs.The development of stable NF-SMAs is crucial for the commercialization of OSCs. By addressing the instability issues, NF-SMAs have the potential to become a viable alternative to fullerenes and enable the development of high-performance, low-cost OSCs.中文回答:非富勒烯小分子受体(NF-SMA)由于其可调的光电性能、易于合成和低成本,作为有机太阳能电池(OSC)中富勒烯的有希望的替代品而备受关注。

白消安对仔猪睾丸曲精小管内增殖分化相关蛋白表达与定位的影响

白消安对仔猪睾丸曲精小管内增殖分化相关蛋白表达与定位的影响

山西农业科学 2023,51(9):1107-1114Journal of Shanxi Agricultural Sciences白消安对仔猪睾丸曲精小管内增殖分化相关蛋白表达与定位的影响任高雅,范小瑞,张警文,张欣荣,贺俊平(山西农业大学 动物医学学院,山西 太谷 030801)摘要:为了研究白消安对仔猪睾丸曲精小管内增殖分化相关蛋白PCNA 、PLZF 和GATA4表达与定位的影响,试验选取体外培养仔猪曲精小管为研究对象,分为对照组和试验组,其中试验组各添加5 mg/kg 白消安,分别培养1、2、3 d ,离心获取曲精小管,采用HE 染色检测形态变化,采用免疫组化、qRT -PCR 和Western blot 法分别检测PCNA 、PLZF 和GATA4表达和定位的变化。

HE 染色结果显示,各试验组曲精小管内均含有支持细胞和生殖细胞;免疫组织化学结果显示,各试验组的PCNA 蛋白定位于生殖细胞和支持细胞的细胞核,白消安作用可导致PCNA 染色变深,表达量升高。

各试验组GATA4蛋白定位于支持细胞的细胞核,且与对照组相比无明显差异;各试验组的PLZF 蛋白定位于生殖细胞的细胞核,与对照组相比,白消安作用2 d 时PLZF 染色无显著差异,白消安作用1、3 d 时PLZF 染色变深,表达量升高。

qRT -PCR 和Western Blot 结果显示,与对照组相比,试验组PCNA 和GATA4 mRNA 及其蛋白表达量均显著升高;白消安作用2 d 的PLZF mRNA 和蛋白表达量差异不显著,白消安作用1、3 d 的PLZF mRN 以及蛋白表达量均显著升高。

综上所述,PCNA 、PLZF 和GATA4均表达于体外培养仔猪曲精小管,白消安作用可导致PCNA 、PLZF 和GATA4在曲精小管内表达水平改变,提示白消安通过影响增殖分化相关蛋白的表达导致猪睾丸精子发生受损。

关键词:白消安;仔猪睾丸曲精小管;Western blot 法;PCNA ;GATA4;PLZF中图分类号:S858.28 文献标识码:A 文章编号:1002‒2481(2023)09‒1107‒08Effects of Busulfan on Expression and Localization of Proliferation and DifferentiationRelated Proteins in Seminiferous Tubules in Testis of PigletsREN Gaoya ,FAN Xiaorui ,ZHANG Jingwen ,ZHANG Xinrong ,HE Junping (College of Veterinary Medicine , Shanxi Agricultural University , Taigu 030801, China )Abstract :To study the effect of busulfan on the expression and localization of the proliferation and differentiation related proteins PCNA, PLZF, and GATA4 in seminiferous tubules in testis of piglets, in this study, seminiferous tubules of piglets cultured in vitro were selected as the research subjects and divided into control group and experimental group. The experimental group was supplemented with 5 mg/kg of busulfan for 1, 2 and 3 days respectively, and seminiferous tubules were obtained by centrifugation. HE staining was used to detect the morphological changes of chromosomes. Immunohistochemistry, qRT -PCR, and Western blot were used to detect the changes in the expression and localization of PCNA , PLZF, and GATA4. HE staining showed that there were both Sertoli cells and germ cells existing in the seminiferous tubules in all experimental groups. Immunohistochemical studies showed that PCNA protein was localized in the nuclei of germ cells and Sertoli cells in all experimental groups. The staining of PCNA became darker and the expression level increased due to the function of busulfan. In the experimental groups, GATA4 protein was located in the nucleus of Sertoli cell, and there was no significant difference in GATA4 protein staining between the experimental group and the control group. PLZF protein was located in nucleus of germ cells of experimental groups. Compared with the control group, PLZF staining showed no significant difference after 2 days of busulfan treatment, while PLZF staining became darker and expression increased after 1 and 3 days of busulfan treatment. The results of qRT -PCR and Western Blot showed that the mRNA and protein expressions of PCNA and GATA4 in the experimental groups were significantly increased compared with the control group. The expression of PLZF mRNA and protein had no significant differences after 2 days of busulfan treatment. The expression of PLZF mRNA and protein was significantly increased after 1 and 3 days of busulfan treatment. In conclusion, PCNA, PLZF, and GATA4 were expressed in seminiferousdoidoi:10.3969/j.issn.1002-2481.2023.09.16收稿日期:2022-12-02基金项目:晋中市科技重点研发计划(农业)(Y192014);山西省重点研发计划项目(201903D221012)作者简介:任高雅(1995-),女,山西长治人,硕士,主要从事动物组织胚胎学研究工作。

Anomalous couplings of type 0 D-branes

a rXiv:h ep-th/9983v14A ug1999ANOMALOUS COUPLINGS OF TYPE 0D-BRANES Marco Bill´o Dipartimento di Fisica Teorica,Universit`a di Torino and I.N.F.N.,Sezione di Torino,via P.Giuria 1,I-10125,Torino,Italy Ben Craps and Frederik Roose Instituut voor Theoretische Fysica Katholieke Universiteit Leuven,B-3001Leuven,Belgium Abstract Closed type 0string theories and their D-branes are introduced.The full Wess-Zumino action of these D-branes is derived.The analogy with type II is emphasized throughout the argument.Type 0Strings and D-branes.Type 0string theory is a non-supersymmetric,modular invariant theory of closed strings.The pres-ence of a tachyonic state in their spectrum makes type 0strings much harder to analyse than the supersymmetric type II strings.Nevertheless,type 0and type II strings have many features in common.In this con-tribution this fact will be exploited to show that type 0D-branes have anomalous terms in their worldvolume action.The analysis is based on Ref.[1],to which we refer for a more detailed treatment and for a more complete list of references.In the Neveu-Schwarz-Ramond formulation,type II string theories are obtained by imposing independent GSO projections on the left and right moving part.This amounts to keeping the following (left,right)sectors:IIB :(NS+,NS+),(R+,R+),(R+,NS+),(NS+,R+);IIA :(NS+,NS+),(R+,R −),(R+,NS+),(NS+,R −),where for instance R ±is the Ramond sector projected with P GSO =(1±(−)F )/2,F being the world-sheet fermion number.12The type0string theories contain instead the following sectors:0B:(NS+,NS+),(NS−,NS−),(R+,R+),(R−,R−);0A:(NS+,NS+),(NS−,NS−),(R+,R−),(R−,R+). These theories do not contain bulk spacetime fermions,which would have to come from“mixed”(R,NS)sectors.The inclusion of the NS-NS sectors with odd fermion numbers means that the closed string tachyon is not projected out.The third difference with type II theories is that the R-R spectrum is doubled.For instance,in the0B case,beside the IIB R-R potentials C p+1contained in bispinors of the(R+,R+)sector, there are the potentials C′p+1from bispinors of the(R−,R−)sector.Note that the bispinors containing the primed and unprimed R-R potentials have opposite chirality.This implies a sign difference in the Poincar´e duality relations among thefield strengths.Thus,for instance,in type 0B there is an unconstrainedfive-formfield strength,whose self-dual (anti-self-dual)part is the unprimed(primed)field strength.For our purposes,convenient combinations of C p+1and C′p+1are(C p+1)±=12(C p+1±C′p+1).(1.1)For p=3these are the electric(+)and magnetic(−)potentials[2].We will adopt this terminology also for other values of p.There turn out to be four types of“elementary”D-branes for each p:an electric and a magnetic one(i.e.,charged under(C p+1)±),and the corresponding antibranes[2].Anomalous Couplings.The open strings stretching between two like branes are bosons,just like the bulkfields of type0.However,a bound-ary state computation shows that fermions appear from strings between an electric and a magnetic brane[2].Thus one could wonder whether there are chiral fermions on the intersection of an electric and a magnetic brane.Consider such an orthogonal intersection with no overall trans-verse directions.If the dimension of the intersection is two or six,the computation reveals that there are precisely enough fermionic degrees of freedom on the intersection to form one chiral fermion.In type II string theory,the analogous computation shows that chi-ral fermions are present on two or six dimensional intersections of two orthogonal branes with no overall transverse directions.That observa-tion has had far reaching ly,the presence of chiral fermions has been shown to lead to gauge and gravitational anoma-lies on those intersections of D-branes[3].In a consistent theory,suchType0D-branes3 anomalies should be cancelled by anomaly inflow.In the present case,the anomaly inflow is provided by the anomalous D-brane couplings in the Wess-Zumino part of the D-brane action[3].These anomalous cou-plings have an anomalous variation localized on the intersections withother branes.To sketch how this anomaly inflow comes about,let us focus on thecase of two type IIB D5-branes(to be denoted by D5and D5’)inter-secting on a string.The Wess-Zumino action on D5contains a term ofthe form D5C2∧Y4,where C2is the R-R two-form potential and Y4a certain four-form involving thefield strength of gaugefield on D5andthe curvature two-forms of the tangent and normal bundles of D5.To beprecise,one should replace this term by D5H3∧ω3,with Y4=dω3and H3the complete gauge-invariantfield strength of C2(which generically differs from dC2).Since the gauge variation of the“Chern-Simons”form ω3is given byδω3=dI2for some two-form I2,the anomalous term on D5have a variation localized on the intersection with D5’:δ D5H3∧ω3= D5dH3∧I2= D5d∗H7∧I2= D5δD5′∧I2,(1.2)which can thus cancel the anomaly due to the chiral fermions living on the intersection.A careful analysis of all the anomalies[3]shows that the anomalous part of the D p-brane action is given,in terms of the formal sum C of the various R-R forms,byS WZ=T pˆA(R T)/ˆA(R N).(1.3)Here T p/κdenotes the D p-brane tension,F the gaugefield on the brane and B the NS-NS two-form.Further,R T and R N are the curvatures of the tangent and normal bundles of the D-brane world-volume,andˆA denotes the A-roof genus.Let us now return to type0string theory.As stated above,here chiral fermions live on intersections of electric and magnetic type0D-branes. The associated gauge and gravitational anomalies on such intersections match the ones for type II D-branes.To cancel them,the minimal cou-pling of a D p-brane to a(p+1)-form R-R potential should be extended to the following Wess-Zumino action[1]:S WZ=T pˆA(R T)/ˆA(R N).(1.4)The±in Eq.(1.4)distinguishes between electric and magnetic branes. Note that T p/κdenotes the tension of a type II D p-brane,which can be computed to be√4The argument that the variation of this action cancels the anomaly on the intersection is a copy of the one described above in the type II case, apart from one slight subtlety.For definiteness,consider the intersection of an electric and a magnetic D5-brane on a string.Varying the elec-tric D5-brane action(exhibiting the(C2)+potential,or rather,itsfield strength(H3)+),onefinds that the variation is localized on the inter-section of the electric D5-brane with branes charged magnetically under the(H3)+field ing Eq.(1.1),the different behaviour under Poincar´e duality of the primed and unprimed R-Rfield strengths shows that these are precisely the branes carrying(electric)(H7)−charge,i.e. what we called the magnetic D5-branes.Schematically,δ D5+(H3)+∧ω3= D5+d(H3)+∧I2= D5+d∗(H7)−∧I2= D5+δD5−∧I2.(1.5)A completely analogous discussion goes through for the variation of the magnetic D5-brane action.AcknowledgmentsB.C.and F.R.would like to thank the organisers for a very nice school,and for financial support.This work was supported by the European Commission TMR programme ERBFMRX-CT96-0045.B.C.is Aspirant FWO-Vlaanderen. References[1]Bill´o,M.,Craps,B.and Roose,F.(1999)On D-branes in type0string theory,Phys.Lett.B457,pp.61-69,hep-th/9902196. [2]Bergman,O.and Gaberdiel,M.R.(1997)A non-supersymmetricopen string theory and S-duality,Nucl.Phys.B499,pp.183-204, hep-th/9701137;Klebanov,I.R.and Tseytlin, A.A.(1999)D-branes and dual gauge theories in type0strings,Nucl.Phys.B546,pp.155-181, hep-th/9811035.[3]Green,M.,Harvey,J.A.and Moore,G.(1997)I-brane inflow andanomalous couplings on D-branes,Class.Quant.Grav.14,pp.47-52, hep-th/9605033;Cheung,Y.K.and Yin,Z.(1998)Anomalies,branes,and currents, Nucl.Phys.B517,pp.69-91,hep-th/9710206.。

遗传育种相关名词中英文对照

遗传育种相关名词中英文对照中英文对照的分子育种相关名词 3"untranslated region (3"UTR) 3"非翻译区 5"untranslated region (5; UTR) 5"非翻译区 A chromosome A 染色体 AATAAA 多腺苷酸化信号aberration 崎变 abiogenesis 非生源说 accessory chromosome 副染色体 accessory nucleus 副核 accessory protein 辅助蛋白 accident variance 偶然变异 Ac-Ds system Ac-Ds 系统 acentric chromosome 无着丝粒染色体acentric fragment 无着丝粒片段 acentric ring 无着丝粒环 achromatin 非染色质 acquired character 获得性状acrocentric chromosome 近端着丝粒染色体 acrosyndesis 端部联会 activating transcription factor 转录激活因子activator 激活剂 activator element 激活单元 activator protein( AP)激活蛋白 activator-dissociation system Ac-Ds 激活解离系统 active chromatin 活性染色质 activesite 活性部位 adaptation 适应 adaptive peak 适应高峰adaptive surface 适应面 addition 附加物 addition haploid 附加单倍体 addition line 附加系 additiveeffect 加性效应 additive gene 加性基因 additive genetic variance 加性遗传方差additive recombination 插人重组additive resistance 累加抗性 adenosine 腺昔adenosine diphosphate (ADP )腺昔二鱗酸adenosine triphosphate( ATP)腺昔三憐酸adjacent segregation 相邻分离A- form DNA A 型 DNAakinetic chromosome 无着丝粒染色体akinetic fragment 无着丝粒片断alien addition monosomic 外源单体生物alien chromosome substitution 外源染色体代换alien species 外源种 alien-addition cell hybrid 异源附加细胞杂种 alkylating agent 焼化剂 allele 等位基因allele center 等位基因中心 allele linkage analysis 等位基因连锁分析 allele specific oligonucleotide(ASO)等位基因特异的寡核苷酸 allelic complement 等位(基因)互补 allelic diversity 等位(基因)多样化 allelic exclusion 等位基因排斥 allelic inactivation 等位(基因)失活 allelic interaction 等位(基因)相互作用allelic recombination 等位(基因)重组 allelicreplacement 等位(基因)置换 allelic series 等位(基因)系列 allelic variation 等位(基因)变异 allelism 等位性 allelotype 等位(基因)型 allodiploid 异源二倍体 allohaploid 异源单倍体 allopatric speciation 异域种alloploidy 异源倍性 allopolyhaploid 异源多倍单倍体allopolyploid 异源多倍体 allosyndesis 异源联会allotetraploid 异源四倍体 alloheteroploid 异源异倍体alternation of generation 世代交替 alternative transcription 可变转录 alternative transcription initiation 可变转录起始 Alu repetitive sequence, Alu family Alu 重复序列,Alu 家族ambiguous codon 多义密码子 ambisense genome 双义基因组 ambisense RNA 双义 RNA aminoacyl-tRNA binding site 氨酰基 tRNA 接合位点 aminoacyl-tRNA synthetase 氨酰基 tRNA 连接酶 amixis 无融合amorph 无效等位基因amphidiploid 双二倍体amphipolyploid 双多倍体amplicon 扩增子amplification 扩增 amplification primer 扩增引物analysis of variance 方差分析 anaphase (分裂)后期anaphase bridge (分裂)后期桥anchor cell 锚状细胞 androgamete 雄配子aneuhaploid 非整倍单倍体aneuploid 非整倍体 animal genetics 动物遗传学annealing 复性 antibody 抗体anticoding strand 反编码链anticodon 反密码子anticodon arm 反密码子臂anticodon loop 反密码子环 antiparallel 反向平行antirepressor 抗阻抑物antisense RNA 反义 RNAantisense strand 反义链 apogamogony 无融合结实apogamy 无配子生殖apomixis 无融合生殖 arm ratio (染色体)臂比artificial gene 人工基因 artificial selection 人工选择 asexual hybridization 无性杂交 asexual propagation 无性繁殖 asexual reproduction 无性生殖assortative mating 选型交配 asynapsis 不联会 asynaptic gene 不联会基因atavism 返祖 atelocentric chromosome 非端着丝粒染色体 attached X chromosome 并连 X 染色体 attachmentsite 附着位点 attenuation 衰减 attenuator 衰减子autarchic gene 自效基因auto-alloploid 同源异源体 autoallopolyploid 同源异源多倍体 autobivalent 同源二阶染色体 auto-diploid 同源二倍体;自体融合二倍体 autodiploidization 同源二倍化autoduplication 自体复制 autogenesis 自然发生autogenomatic 同源染色体组 autoheteroploidy 同源异倍性autonomous transposable element 自主转座单元autonomously replicating sequence(ARS)自主复制序列autoparthenogenesis 自发单性生殖 autopolyhaploid 同源多倍单倍体 autopolyploid 同源多倍体 autoradiogram 放射自显影图 autosyndetic pairing 同源配对 autotetraploid 同源四倍体 autozygote 同合子 auxotroph 营养缺陷体 B chromosome B 染色体 B1,first backcross generation 回交第一代 B2,second backcross generation 回交第二代back mutation 回复突变 backcross 回交backcross hybrid 回交杂种 backcross parent 回交亲本 backcross ratio 回交比率 background genotype 背景基因型 bacterial artification chromosome( BAC )细菌人工染色体Bacterial genetics 细菌遗传学 Bacteriophage 噬菌体balanced lethal 平衡致死 balanced lethal gene 平衡致死基因 balanced linkage 平衡连锁 balanced load 平衡负荷balanced polymorphism 平衡多态现象 balanced rearrangements 平衡重组balanced tertiary trisomic 平衡三级三体balanced translocation 平衡异位balancing selection 平衡选择band analysis 谱带分析 banding pattern (染色体)带型basal transcription apparatus 基础转录装置 base analog 碱基类似物base analogue 类減基base content 减基含量base exchange 碱基交换 base pairing mistake 碱基配对错误 base pairing rules 碱基配对法则 base substitution 减基置换 base transition 减基转换 base transversion 减基颠换 base-pair region 碱基配对区base-pair substitution 碱基配对替换 basic number of chromosome 染色体基数 behavioral genetics 行为遗传学behavioral isolation 行为隔离 bidirectionalreplication 双向复制 bimodal distribution 双峰分布binary fission 二分裂binding protein 结合蛋白binding site 结合部位 binucleate phase 双核期biochemical genetics 生化遗传学 biochemical mutant 生化突变体biochemical polymorphism 生化多态性 bioethics 生物伦理学 biogenesis 生源说 bioinformatics 生物信息学biological diversity 生物多样性 biometrical genetics 生物统计遗传学(简称生统遗传学) bisexual reproduction 两性生殖 bisexuality 两性现象 bivalent 二价体 blending inheritance 混合遗传 blot transfer apparatus 印迹转移装置 blotting membrane 印迹膜 bottle neck effect 瓶颈效应 branch migration 分支迁移 breed variety 品种breeding 育种,培育;繁殖,生育 breeding by crossing 杂交育种法 breeding by separation 分隔育种法 breeding coefficient 繁殖率 breeding habit 繁殖习性 breeding migration 生殖回游,繁殖回游 breeding period 生殖期breeding place 繁殖地 breeding population 繁殖种群breeding potential 繁殖能力,育种潜能 breeding range繁殖幅度 breeding season 繁殖季节 breeding size 繁殖个体数 breeding system 繁殖系统 breeding true 纯育breeding value 育种值 broad heritability 广义遗传率bulk selection 集团选择 C0,acentric 无着丝粒的Cl,monocentric 单着丝粒 C2, dicentric 双着丝粒的C3,tricentric 三着丝粒的 candidate gene 候选基因candidate-gene approach 候选基因法 Canpbenmodel 坎贝尔模型carytype 染色体组型,核型 catabolite activator protein 分解活化蛋白catabolite repression 分解代谢产物阻遏catastrophism 灾变说 cell clone 细胞克隆 cell cycle 细胞周期 cell determination 细胞决定 cell division 细胞分裂 cell division cycle gene(CDC gene) 细胞分裂周期基因 ceU division lag 细胞分裂延迟 cell fate 细胞命运cell fusion 细胞融合 cell genetics 细胞的遗传学 cell hybridization 细胞杂交 cell sorter 细胞分类器 cell strain 细胞株 cell-cell communication 细胞间通信center of variation 变异中心 centimorgan(cM) 厘摩central dogma 中心法则 central tendency 集中趋势centromere DNA 着丝粒 DNA centromere interference 着丝粒干扰centromere 着丝粒 centromeric exchange ( CME)着丝粒交换centromeric inactivation 着丝粒失活 centromeric sequence( CEN sequence)中心粒序列 character divergence 性状趋异chemical genetics 化学遗传学chemigenomics 化学基因组学chiasma centralization 交叉中化chiasma terminalization 交叉端化chimera 异源嵌合体Chi-square (x2) test 卡方检验 chondriogene 线粒体基因 chorionic villus sampling 绒毛膜取样 chromatid abemition 染色单体畸变chromatid break 染色单体断裂chromatid bridge 染色单体桥chromatid interchange 染色单体互换 chromatid interference 染色单体干涉 chromatid segregation 染色单体分离chromatid tetrad 四分染色单体chromatid translocation 染色单体异位chromatin agglutination 染色质凝聚chromosomal aberration 染色体崎变chromosomal assignment 染色体定位chromosomal banding 染色体显带chromosomal disorder 染色体病chromosomal elimination 染色体消减 chromosomal inheritance 染色体遗传chromosomal interference 染色体干扰chromosomal location 染色体定位chromosomal locus 染色体位点 chromosomal mutation 染色体突变chromosomal pattern 染色体型chromosomal polymorphism 染色体多态性 chromosomal rearrangement 染色体质量排chromosomal reproduction 染色体增殖chromosomal RNA 染色体 RNAchromosomal shift 染色体变迁,染色体移位chromosome aberration 染色体畸变 chromosome arm 染色体臂chromosome association 染色体联合chromosome banding pattern 染色体带型chromosome behavior 染色体动态chromosome blotting 染色体印迹chromosome breakage 染色体断裂chromosome bridge 染色体桥 chromosome coiling 染色体螺旋chromosome condensation 染色体浓缩chromosome constriction 染色体缢痕chromosome cycle 染色体周期chromosome damage 染色体损伤chromosome deletion 染色体缺失chromosome disjunction 染色体分离chromosome doubling 染色体加倍chromosome duplication 染色体复制chromosome elimination 染色体丢失 chromosome engineering 染色体工程chromosome evolution 染色体进化 chromosome exchange 染色体交换chromosome fusion 染色体融合 chromosome gap 染色体间隙chromosome hopping 染色体跳移chromosome interchange 染色体交换chromosome interference 染色体干涉chromosome jumping 染色体跳查chromosome knob 染色体结 chromosome loop 染色体环chromosome lose 染色体丢失chromosome map 染色体图 chromosome mapping 染色体作图chromosome matrix 染色体基质chromosome mutation 染色体突变 chromosome non-disjunction 染色体不分离 chromosome paring 染色体配对chromosome polymorphism 染色体多态性 chromosome puff 染色体疏松 chromosome rearrangement 染色体质量排chromosome reduplication 染色体再加倍 chromosome repeat 染色体质量叠 chromosome scaffold 染色体支架chromosome segregation 染色体分离 chromosome set 染色体组chromosome stickiness 染色体粘性chromosome theory of heredity 染色体遗传学说chromosome theory of inheritance 染色体遗传学说chromosome thread 染色体丝chromosome walking 染色体步查chromosome-mediated gene transfer 染色体中介基因转移 chromosomology 染色体学 CIB method CIB 法;性连锁致死突变出现频率检测法 circular DNA 环林 DNA cis conformation 顺式构象 cis dominance 顺式显性 cis-heterogenote 顺式杂基因子 cis-regulatory element 顺式调节兀件 cis-trans test 顺反测验cladogram 进化树 cloning vector 克隆载体 C-meiosis C 减数分裂C-metaphase C 中期C-mitosis C 有丝分裂 code degeneracy 密码简并coding capacity 编码容量 coding ratio 密码比 coding recognition site 密码识别位置 coding region 编码区coding sequence 编码序列 coding site 编码位置 coding strand 密码链 coding triplet 编码三联体 codominance 共显性 codon bias 密码子偏倚 codon type 密码子型coefficient of consanguinity 近亲系数 coefficient of genetic determination 遗传决定系数 coefficient of hybridity 杂种系数 coefficient of inbreeding 近交系数coefficient of migration 迁移系数 coefficient of relationship 亲缘系数 coefficient of variability 变异系数 coevolution 协同进化 coinducer 协诱导物 cold sensitive mutant 冷敏感突变体colineartiy 共线性combining ability 配合力comparative genomics 比较基因组学competence 感受态competent cell 感受态细胞competing groups 竞争类群 competition advantage 竞争优势competitive exclusion principle 竞争排斥原理complementary DNA (cDNA)互补 DNAcomplementary gene 互补基因 complementation test 互补测验complete linkage 完全连锁 complete selection 完全选择 complotype 补体单元型 composite transposon 复合转座子 conditional gene 条件基因 conditional lethal 条件致死conditional mutation 条件突变 consanguinity 近亲consensus sequence 共有序列 conservative transposition 保守转座 constitutive heterochromatin 组成型染色质continuous variation 连续变异convergent evolution 趋同进化cooperativity 协同性 coordinately controlled genes 协同控制基因 core promoter element 核心启动子 core sequence 核心序列 co-repressor 协阻抑物correlation coefficient 相关系数 cosegregation 共分离 cosuppression 共抑制cotranfection 共转染cotranscript 共转录物 cotranscriptional processing 共转录过程 cotransduction 共转导cotransformation 共转化 cotranslational secrection 共翻译分泌counterselection 反选择coupling phase 互引相 covalently closed circular DNA(cccDNA)共价闭合环状 DNAcovariation 相关变异criss-cross inheritance 交叉遗传 cross 杂交crossability 杂交性crossbred 杂种cross-campatibility 杂交亲和性 cioss-infertility 杂交不育性 crossing over 交换crossing-over map 交换图crossing-over value 交换值crossover products 交换产物 crossover rates 交换率crossover reducer 交换抑制因子crossover suppressor 交换抑制因子crossover unit 交换单位 crossover value 值crossover-type gamete 交换型配子C-value paradox C 值悖论 cybrid 胞质杂种 cyclin 细胞周期蛋白cytidme 胞苷 cytochimera 细胞嵌合体cytogenetics 细胞遗传学 cytohet 胞质杂合子cytologic 细胞学的cytological map 细胞学图cytoplasm 细胞质cytoplasmic genome 胞质基因组 cytoplasmic heredity 细胞质遗传 cytqplasmic incompatibility 细胞质不亲和性cytoplasmic inheritance 细胞质遗传cytoplasmic male sterility 细胞质雄性不育cytoplasmic mutation 细胞质突变 cytofdasmic segregation 细胞质分离cytoskeleton 细胞骨架Darwin 达尔文 Darwinian fitness 达尔文适合度Darwinism 达尔文学说 daughter cell 子细胞 daughter chromatid 子染色体 daughter chromosome 子染色体deformylase 去甲酰酶 degenerate code 简并密码degenerate primer 简并引物 degenerate sequence 简并序列 degenerated codon 简并密码子degeneration 退化 degree of dominance 显性度delayed inheritance 延迟遗传 deletant 缺失体deletion 缺失。

Food Molecular Biology智慧树知到答案章节测试2023年华南理工大学

第一章测试1.The template strand has a sequence complementary to that of the RNAtranscript.()A:对B:错答案:A2.The coding strand has the same sequence as that of the RNA transcript.()A:对B:错答案:B3.Chromosome contains a linear array of genes and each gene resides at aparticular location on the chromosome.()A:错B:对答案:B4.Transposable elements (TEs), also known as “jumping genes,” are DNAsequences that move from one location on the genome to another location.()A:错B:对答案:B5.DNA polymerase are essential for DNA replication and usually work in pairsto create two identical DNA strands from a single original DNA molecule.()A:对B:错答案:A第二章测试1.DNA sequences that are highly enriched in G–C base pairs typically have highmelting temperatures. Therefore, PCR amplification is greatly hindered bythe presence of G–C-rich regions within the template.()A:对B:错答案:A2.The lacZ gene can be used to screen bacteria containing recombinantplasmids. A special plasmid carries a copy of the lacZ gene and an ampicillin-resistance gene.()A:对B:错答案:A3.We use Lipid mediated gene delivery as example. It uses lipids to cause a cellto absorb exogenous DNA since they are both made of a phospholipid bilayer.A:对B:错答案:A4.When you doing transgenic plant, you could do overexpression, gene knock-down or gene knock out. Overexpression usually refers to an experimentwhen DNA is added to the cell to force expression of the gene to a muchhigher than normal level.()A:错B:对答案:B5.The technique we use for gene knock down is small interfering RNA (siRNA).Sometimes we call short interfering RNA or silencing RNA, it is a class ofsingle-stranded RNA non-coding RNA molecules, 20-25 base pairs in length, and operating within the RNA interference (RNAi) pathway.()A:对B:错答案:B第三章测试1.In the process of electrophoresis, the protein with the smallest molecularweight moves the slowest.()A:对B:错答案:B2.The antibody consists of two heavy chains, two light chains and hinge region.()A:错B:对答案:B3.Most antigens have several epitopes.()A:对B:错答案:A4.In the mass spectrometry, the smaller ion requires less time to traverse thechamber.()A:错B:对答案:B5.X-ray crystallography is only suitable for the determination of crystalstructure.()B:对答案:B第四章测试1.Which type of cells is primarily responsible for nutrient sensing? ()A:Paneth cellsB:Mast cellsC:Stem cellsD:Enteroendocrine cells答案:D2.( ) is the basic architectural unit of the liverA:Liver sinusoidB:Kupffer cellsC:Portal veinD:Liver lobule答案:D3.The liver can only metabolize protein and lipid. ( )A:对B:错答案:B4.( ) can induce NAFLD.A:Hight alcoholB:Rich in sucroseC:High fructoseD:High saturated fat答案:BCD5.What are the centers of metabolism?A:Pancreas, brain, muscle and liverB:Pancreas, brain, muscle, adipose tissue, kidney and liverC:Pancreas, brain, muscle, adipose tissue and liverD:Pancreas, muscle, adipose tissue and liver答案:C第五章测试1.What is the physiological concentration range of hydrogen peroxide H2O2?()A:10 nMB:1 nMC:100 nMD:1000 nM答案:C2.All polyphenols are absorbed with equal efficacy. ()A:对B:错答案:B3.Proanthocyanidins are well absorbed in small intestine. ()A:对B:错答案:B4.The polyphenol has been strongly demonstrated to benefit cancer patients.()A:错B:对答案:A5.Where does IDH1 work? ( )A:MitochondriaB:CytoplasmC:Outside the cellD:Nucleus答案:B第六章测试1.There two types of Immune response, including Innate immunity andadaptive immunity. ()A:对B:错答案:A2.Antibodies possess distinct antigen-binding and effector units. ()A:错B:对答案:B3.Antibodies Bind Specific Molecules Through Hypervariable Loops. ()A:对B:错答案:A4.The amino-terminal immunoglobulin domains of each chain is referred to asthe constant regions.()A:对B:错答案:B5.IgG fold consists of a pair of β sheets, each built of antiparallel b strands, thatsurround a central hydrophobic core.()A:错B:对答案:B第七章测试1.The nutrients in food mainly include water, sugars, proteins, fats, inorganicsalts, vitamins and crude cellulose. Although the crude cellulose cannot bedigested and absorbed by the human body, it has a very importantphysiological effect on the human body. The following foods are rich in crude fiber.()A:Spinach. CeleryB:Eggs. PorkC:Milk. BeefD:Fish. Shrimp答案:A2.Beef contains a lot of phenolic compounds.()A:错B:对答案:A3.The major flavonols are()A:FlavanonesB:MyricetinC:KaempferolD:Quercetin答案:ABCD4.The most abundant hydroxycinnamic acid derivative in plant foods is anester of caffeic and quinic acids.()A:错B:对答案:B5.Obesity is defined when BMI exceeds which of the following values().A:28 kg/m2B:25 kg/m2C:32 kg/m2D:30 kg/m2答案:D。

生物英语测试题及答案解析

生物英语测试题及答案解析一、选择题(每题2分,共20分)1. What is the basic unit of life?A. CellB. OrganC. TissueD. System2. Which of the following is not a characteristic of living organisms?A. GrowthB. ReproductionB. Response to stimuliD. Inability to move3. What is the process by which plants make their food?A. RespirationB. PhotosynthesisC. FermentationD. Digestion4. In the field of genetics, what does the term "gene" refer to?A. A unit of heredityB. A type of proteinC. A form of energyD. A cell structure5. Which of the following is a type of mutation?A. Natural selectionB. Genetic driftC. Chromosomal mutationD. All of the above6. What is the function of chlorophyll in plants?A. To store waterB. To provide energy for photosynthesisC. To protect against sunlightD. To store nutrients7. What is the term for the study of the relationships among living organisms?A. AnatomyB. PhysiologyC. EcologyD. Taxonomy8. Which of the following is a type of cell division?A. MitosisB. MeiosisC. Both A and BD. None of the above9. What is the main component of the cell membrane?A. ProteinsB. CarbohydratesC. LipidsD. Nucleic acids10. What is the process by which organisms produce offspring that have genetic material from both parents?A. Asexual reproductionB. Sexual reproductionC. CloningD. Parthenogenesis答案解析:1. A. Cell - Cells are the smallest unit of life that can carry out all the functions necessary for life.2. D. Inability to move - Living organisms have the ability to move, grow, reproduce, and respond to stimuli.3. B. Photosynthesis - Plants convert light energy into chemical energy stored in glucose.4. A. A unit of heredity - Genes are segments of DNA that determine traits.5. C. Chromosomal mutation - Mutations can occur at the level of genes or entire chromosomes.6. B. To provide energy for photosynthesis - Chlorophyll absorbs light and is essential for the process of photosynthesis.7. C. Ecology - The study of the interactions between organisms and their environment.8. C. Both A and B - Mitosis is cell division that results in two identical daughter cells, while meiosis produces fournon-identical cells for sexual reproduction.9. C. Lipids - The cell membrane is primarily composed of a phospholipid bilayer.10. B. Sexual reproduction - This process combines genetic material from two parents to create offspring with a unique genetic makeup.二、填空题(每空1分,共10分)1. The process by which organisms use oxygen to break down glucose is called __________.2. The largest organ in the human body is the __________.3. In genetics, the dominant allele is the one that__________.4. The scientific name for a species is given in __________ nomenclature.5. The study of the internal structures of organisms iscalled __________.答案解析:1. Cellular respiration - This is the process where cells convert glucose into energy.2. Skin - The skin is the largest organ by area and weight in the human body.3. Masks the effect of the recessive allele - The dominant allele is expressed in the phenotype even when paired with a recessive allele.4. Binomial - Each species has a two-part name, with thefirst part being the genus and the second part being the species.5. Anatomy - This field studies the structures and functions of the parts of organisms.三、简答题(每题5分,共30分)1. Explain the difference between prokaryotic and eukaryotic cells.2. What is the role of DNA in the cell?3. Describe the process of mitosis in a eukaryotic cell.4. How does natural selection contribute to evolution?答案解析:1. Prokaryotic cells lack a nucleus and membrane-bound organelles, while eukaryotic cells have a nucleus and various membrane-bound organelles such as mitochondria and the endoplasmic reticulum.2. DNA carries genetic information that codes for the synthesis of proteins, which are essential for the structure, function, and regulation of the organism's cells, tissues, and organs.3.。

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a
C ∧ dT ∧ e2πα′F +B ∧ Aˆ(RT )/Aˆ(RN ) .
p+1
(1.3)
It involves the topological density ∂xT (x), which is localized at the core of the kink and is such that dT (x) = ±2T0. In the limit of zero size, dT (x) = 2T0δ(x − x0)dx, and the above action takes the form of the usual Wess-Zumino effective action for a BPS D(p − 1)-brane, localized
arXiv:hep-th/9908029v1 4 Aug 1999
ANOMALOUS COUPLINGS OF NON-BPS D-BRANES
Marco Bill´o
Dipartimento di Fisica Teorica, Universita` di Torino and I.N.F.N., Sezione di Torino, via P. Giuria 1, I-10125, Torino, Italy
monopole, is accompanied by a non-trivial SU(2) gauge field:
T (x) = f (r)σaxa , Aai (x) = h(r)ǫaij xj ,
(1.5)
where r is the radial distance in the three transverse directions; the prefactors f (r) and h(r) go to constants for r → 0, while f (r) ∼ T0/r and h(r) ∼ 1/r2 for r → ∞. The field-strength in the unbroken U(1)
vortex, are classified by the non-trivial embeddings of the “sphere at infinity” S∞2 into the vacuum manifold, namely by π2(V) = Z.
Apart from the “center of mass” U(1) subgroup, we are in the situation of the Georgi-Glashow model, where the tachyon field T (x) = T a(x)σa (σa being the Pauli matrices) sits in the adjoint of SU(2), and the vacuum manifold is described by T aT a = T02. The vortex configuration of winding number one of the tachyon, which is the ’t Hooft-Polyakov
In [5] we argued that all type II non-BPS branes couple universally to Ramond-Ramond fields as given by1
SW ′ Z = a
C ∧ d Tr T e2πα′ F +B ∧ Aˆ(RT )/Aˆ(RN ) ,
p+1
(1.2)
where T is the real, adjoint tachyon field living on the non-BPS brane and a is a constant. Let us indicate how the R-R couplings of eq. (1.2) account for the R-R couplings (1.1) of the stable lower-dimensional brane that emerges from the process of tachyon condensation. The cases Dp → D(p − 1) and Dp → D(p − 3) will be treated in detail. It will turn out, for instance, that the R-R charges of the D8-branes and D6-branes one constructs from unstable D9-branes [4] have the expected ratio.
1
2
of the tangent and normal bundles of the D-brane world-volume, and Aˆ denotes the A-roof genus.
As for type IIA, Horava described in [4] how to construct BPS D(p − 2k − 1)-branes as bound states of (sufficiently many) unstable Dp-branes (and thus how to construct all type IIA D-branes in terms of D9-branes). The lower-dimensional BPS branes arise as the result of the condensation of a tachyon field into a vortex configuration, accompanied by non-trivial gauge fields. In this case, it was not clear how the lower-dimensional BPS branes acquire the R-R couplings of eq. (1.1).
Non-BPS D-branes 3
As a less trivial example, let us start from two unstable Dp-branes.
The tachyon field T , transforming in the adjoint of the U(2) gauge group,
can form a non-trivial vortex configuration in co-dimension three. The
tachyon potential is assumed to be such that the minima of T have the
eigenvalues (T0, −T0), so that the vacuum manifold is V = U(2)/(U(1) × U(1)) = S2. The possible stable vortex configurations T (x), depending on 3 coordinates xi transverse to the (p − 2)-dimensional core of the
For type IIB this was demonstrated by Witten in [2], where all branes were built from sufficiently many D9–anti-D9 pairs. In this set-up, the Dp-brane that emerges via a process of tachyon condensation inherits its anomalous Wess-Zumino couplings to the R-R fields [3],
Ben Craps and Frederik Roose
Instituut voor Theoretische Fysica Katholieke Universiteit Leuven, B-3001 Leuven, Belgium
Abstract
Non-BPS type II D-branes couple to R-R potentials via an action that, upon tachyon condensation, gives rise to the Wess-Zumino action of BPS D-branes.
Consider first a single non-BPS Dp-brane. There is a real tachyon field living on its worldvolume. The tachyon potential is assumed to be such that the vacuum manifold consists of the two points {T0, −T0}. The tachyon can condense in a non-trivial (anti)-kink configuration T (x) depending on a single coordinate. The R-R coupling (1.2) on the Dpbrane reads in this case
SWZ
=
Tp κ
C ∧ Tr e2πα′ F )/Aˆ(RN ) ,
(1.1)
from the analogous couplings of the parent branes. In eq. (1.1), Tp/κ denotes the Dp-brane tension, C a formal sum of R-R potentials, F the gauge field on the brane and B the NS-NS two-form. The trace is over the Chan-Paton indices. Further, RT and RN are the curvatures
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