温度和土壤水分对银杏叶黄酮类化合物积累的影响

以2年生银杏实生苗为试材,在人工气候室内采用土培盆栽试验方法,研究了温度和土壤水分对银杏叶黄酮类化合物积累的影响.试验设置土壤含水量(W)和温度(T)各3个梯度,W₁、W₂、W₃分别为田间持水量的55%～60%、40%～45%、30%～35%;T₁、T₂、T₃白天和夜间的温度分别为15/5 ℃、25/15 ℃、35/25 ℃.结果表明: T₁温度条件下,各土壤水分处理的银杏叶中的槲皮素、山奈酚、异鼠李素和总黄酮含量普遍高于T₂和T₃,而土壤水分对银杏叶中各种黄酮类化合物积累的影响不显著;银杏叶中黄酮类化合物以山奈酚含量最高,其次为槲皮素和异鼠李素;T₃温度下银杏单株总黄酮产量普遍高于T₂和T₁.在收获前适当采取土壤覆盖和灌水等措施降低种植园的温度,有利于提高银杏叶中黄酮的含量,增加单位面积黄酮的产量.     

杉木解酚菌的研究

从杉木林土壤中筛选到5株高效解酚菌(F₂、F₃、F₄、F₇、F₁₅),结果表明,F₄、Fd,F₂、F₁₅5d能将600rng·L^-1的阿魏酸降解完,F₇的降解率为91.3%;F₄、F₃、F₂、F₇d,F₁₅、4d能将600mg·L^-1的对羟基苯甲酸完全降解;5株解酚菌对邻香草醛的降解能力较弱,除F₂5d能将300mg·L^-1的邻香草醛完全降解外,其余4株5d的降解率为83%～96%.同时发现,F₄能抑制杉苗生长,而其余4株则能在不同条件下促进杉苗生长,将5种菌按等比例混合使用,在土壤添加酚酸的情况下,仍能促进菌根苗Z和非菌根苗生长,杉木苗干重增长率为8.9%～168%.     

基于超声清洗的树木叶面颗粒物粒径分布与吸滞效率研究——以银杏和油松为例

明确在常规叶片清洗方法(泡洗或泡洗+刷洗)上增加超声清洗对叶面各径级颗粒物滞纳量定量评估的影响, 并在此基础上研究叶面颗粒物的粒径分布和吸滞效率, 可进一步提高城市树木大气颗粒物吸滞能力的定量评估精度。该文以城市森林建设常用阔叶树种银杏(Ginkgo biloba)和针叶树种油松(Pinus tabuliformis)为研究对象, 于雨后(降水量>15 mm) 4天(短滞尘时长)和14天(长滞尘时长)分别采集叶样, 并依次对其进行泡洗(WC)、刷洗(BC)、超声清洗(UC)等洗脱程序, 然后对每个清洗步骤下叶片洗脱液中颗粒物的质量和粒径分布进行测试, 并依此估算叶片各径级颗粒物的吸滞效率。结果表明, 以“泡洗+刷洗+超声清洗”清洗流程的测试结果为参照, 若只对叶片进行泡洗, 则银杏和油松对大气颗粒物(PM₁, 粒径d ≤1 µm)、PM_2.5 (d ≤ 2.5 µm)、PM₅ (d ≤ 5 µm)、PM₁₀ (d ≤ 10 µm)吸滞量会分别被低估约一半(54%、53%、53%和53%)和40% (42%、42%、42%和42%); 若只进行“泡洗+刷洗”, 则银杏和油松对相应径级颗粒物的吸滞量仍会分别被低估约15% (17%、16%、15%和15%)和20% (21%、20%、20%和20%)。油松叶面颗粒物粒径分布呈双峰曲线, 而银杏叶面颗粒物粒径则呈单峰分布, 且银杏叶面颗粒物平均粒径在短、长滞尘时长下均大于油松。油松叶片对PM₁、PM_2.5、PM₅、PM₁₀和总悬浮颗粒物的吸滞效率分别为8.96、23.92、23.96、23.96和23.96 mg·m^-2·d^-1, 分别比银杏叶片高112%、73%、34%、37%和42%。     

越冬期测墒补灌对小麦耗水特性和光合有效辐射截获利用的影响

于2013—2014和2014—2015年两个小麦生长季进行田间试验,供试品种为‘济麦22’,设置5个处理,分别为W₀(全生育期不灌水)、W₁(越冬期不灌水,拔节期和开花期分别补灌至0～40 cm土层土壤相对含水量为65%和70%)、W₂(越冬期、拔节期和开花期分别补灌至土壤相对含水量为70%、65%和70%)、W₃(越冬期、拔节期和开花期分别补灌至土壤相对含水量为75%、65%和70%)和W₄(越冬期、拔节期和开花期均定量灌溉60 mm),研究越冬期测墒补灌对小麦耗水特性和光合有效辐射截获利用的影响.结果表明: 总灌水量及其占总耗水量的比例为W₄＞W₃＞W₂＞W₁＞W₀;土壤贮水消耗量占总耗水量的比例为W₀＞W₁、W₂＞W₃、W₄;总耗水量和开花至成熟期的耗水量均为W₄＞W₂、W₃＞W₁＞W₀.两生长季小麦开花后冠层光合有效辐射(PAR)截获率为W₄＞W₂、W₃＞W₁＞W₀,而花后冠层PAR反射率各处理间的表现与之相反.灌水处理中干物质净积累量为W₄处理最高,W₁处理最低.两生长季小麦越冬期0～40 cm土层土壤相对含水量补灌至70%的W₂处理籽粒产量仅低于定量灌溉的W₄处理,水分利用效率和灌溉效益最高,是本试验条件下节水高产的最优处理.     

测墒补灌对小麦旗叶光合特性及酶活性的影响

以‘济麦20’为供试材料,通过田间试验,在拔节期和开花期设置土壤相对含水量为65%(W₆₅)、70%(W₇₀)和75%(W₇₅)的测墒补灌处理,以全生育期不灌溉为对照(CK),研究不同测墒补灌水平对旗叶光合特性及酶活性的影响.结果表明: W₇₀处理小麦旗叶净光合速率、蔗糖含量和磷酸蔗糖合成酶(SPS)活性在花后14～21 d均显著高于其他处理.成熟期W70处理干物质量与W₇₅处理无显著差异,但显著高于W₆₅处理和CK;W₇₀处理单茎质量显著高于其他处理.W₇₀处理超氧化物歧化酶和过氧化氢酶活性及可溶性蛋白含量在花后14～28 d显著高于其他处理,丙二醛含量在花后14～28 d显著低于CK和W₆₅处理,与W₇₅处理无显著差异.2012—2013年和2013—2014年W₇₀处理小麦籽粒产量分别为8941.4和9125.4 kg·hm^-2,与W₇₅处理无显著差异,显著高于W₆₅处理和CK;W₇₀处理水分利用效率显著高于其他处理.在本试验条件下,拔节期和开花期0
～140 cm土层平均土壤相对含水量均以70%为节水高产高效的最佳灌溉处理.     

不同土层测墒补灌对冬小麦耗水特性及产量的影响

于2010-2011年选用高产小麦品种济麦22进行大田试验,设置0～20 cm（W₁）、0～40 cm（W₂）、0～60 cm（W₃）和0～140 cm（W₄）4个测墒补灌土层,于越冬期（目标相对含水量均为75%）、拔节期（目标相对含水量均为70%）和开花期（目标相对含水量均为70%）进行测墒补灌,以全生育期不灌水处理（W₀）为对照,研究不同土层测墒补灌对冬小麦耗水特性及产量的影响.结果表明： 小麦越冬期、拔节期和开花期补充灌水量为W₃>W₂>W₁,W₄处理小麦越冬期和拔节期补充灌水量较少,但开花期补灌量显著高于其他处理;全生育期补灌量占总耗水量的比例为W₄、W₃>W₂>W₁.土壤水消耗量占总耗水量的比例为W₁>W₂>W₃>W₄;随测墒补灌土层深度的增加,土壤水消耗量占总耗水量的比例减少;W₂处理80～140 cm和160～200 cm土层土壤水消耗量显著高于W₃和W₄处理.各处理的总补灌量为W₃>W₄>W₂>W₁;籽粒产量为W₂、W₃、W₄>W₁>W₀,W₂、W₃、W₄间无显著差异;水分利用效率为W₂、W₄>W₀、W₁>W₃,W₂与W₄之间无显著差异.综合考虑灌水量、籽粒产量和水分利用效率,W₂处理是本试验条件下的最佳处理,即以0～40 cm土层测墒补灌效果最优.     

CO2浓度和土壤含水量对植物个体尺度短期水分利用效率的影响

分析植物个体短期水分利用效率(WUE_p)对CO₂浓度(C_a)和土壤含水量(SWC)的响应,可提高对气候变化下个体生存策略的认识。本研究以侧柏幼树为对象,在模拟气候箱中进行培养试验,设400(C₄₀₀)、600(C₆₀₀)和800 μmol·mol^-1CO₂(C₈₀₀)浓度处理和35%～45%田间持水量(FC)、50%～60%FC、60%～70%FC、70%～80%FC、95%～100%FC土壤含水量处理,共15个处理。WUE_p对C_a和SWC的响应用包裹式茎流计、称重法结合静态同化箱测定。结果表明: 个体日间(0.12～1.87 mol·h^-1)和夜间蒸腾速率(0.01～0.16 mol·h^-1)均在C₄₀₀×70%～80%FC时达到最大值,个体日间净光合速率(2.12～22.10 mmol·h^-1)在C₈₀₀×70%～80%FC时达到最大值,而个体夜间呼吸速率(0.84～4.41 mmol·h^-1)随SWC的增加而增加,随C_a的增加而减小,在C₄₀₀×95%～100%FC时达到最大值。WUE_p(5.37～24.35 mmol·mol^-1)在C₈₀₀×50%～60%FC时达到最大值,表明高C_a和干旱条件下,植物个体可通过生理可塑性调整,利用较少的水分固定更多的碳;此外,当个体间形态特征差异较小时,叶片瞬时水分利用效率可以较好地指示WUE_P的变化。     

红花桑寄生叶提取物的抗氧化活性及酚类物质分析

采用DPPH法、TEAC法、FRAP法对红花桑寄生叶不同溶剂提取物的抗氧化活性进行体外评价,并测定其总酚、总黄酮含量。结果表明,溶剂种类对红花桑寄生叶提取物的得率、总酚、总黄酮及抗氧化活性影响显著。在3种评价方法中,不同溶剂提取物的抗氧化活性均表现出不同程度的量效依赖关系。3种溶剂提取物的抗氧化活性强弱依次为丙酮提取物 >甲醇提取物 >水提取物,其中80%丙酮提取物(总酚含量最高,达276.83mg/g)抗氧化活性最强,清除DPPH自由基能力EC₅₀值为0.247,FRAP值(FeSO₄ mmol/100g)为115.81,浓度为1.0mg/ml时,TEAC值为2.04。     

不同土层测墒补灌对冬小麦耗水特性与光合速率和产量的影响

于2012—2014年两个冬小麦生长季,在大田条件下设置：全生育期不灌水(W₀)处理,当地定量节水灌溉(拔节期和开花期均灌水60 mm,W₁)处理,依据0～20 cm (W₂)、0～40 cm (W₃)、0～60 cm (W₄)和0～140 cm (W₅)土层土壤含水量测墒补灌处理,于拔节期和开花期补灌至土壤相对含水量为田间持水量的65%和70%,研究依据不同土层土壤含水量测墒补灌对冬小麦耗水特性、光合速率和籽粒产量的影响.结果表明：各处理拔节期灌水量为W₁、W₄＞W₃＞W₂、W₅,开花期灌水量和总灌水量均为W₅＞W₁、W₄＞W₃＞W₂,W₃总耗水量显著高于W₂处理,与W₁、W₄和W₅处理无显著差异.W₃土壤贮水消耗量高于W₁、W₄和W₅处理,其中,W₃在拔节至开花阶段和开花至成熟阶段对40～140 cm和60～140 cm土层土壤贮水消耗量均显著高于其余灌水处理.灌浆中期W₃处理小麦旗叶光合速率、蒸腾速率和水分利用效率最高,W₁和W₄处理次之,W₀处理最低.W₃处理两个生长季的籽粒产量分别为9077和9260 kg·hm^-2,水分利用效率分别为20.7和20.9 kg·hm-2·mm^-1,均显著高于其余处理,灌溉水生产效率最高.综合考虑灌水量、籽粒产量和水分利用效率,小麦拔节期和开花期适宜进行测墒补灌的土层深度为0～40 cm.     

不同施氮水平下杨树-苋菜间作系统对土壤氮素流失的影响

采用田间试验方法,研究了杨树 苋菜间作系统,即株行距2 m×5 m(L₁)和2 m×15 m(L₂)在0(N₀)、91(N₁)、137(N₂)和183(N₃) kg·hm^-2施氮水平下的土壤氮素流失特征.结果表明: 不同施氮水平对地表径流量、淋溶量和土壤侵蚀量的控制效果均为L₁＞L₂＞L₃ (单作苋菜);L₁、L₂地表径流量分别比L₃降低65.1%、55.9%;L₁、L₂距林带0.5 m处淋溶量比L₃降低30.0%、28.9%,距林带1.5 m处淋溶量比L₃降低25.6%、21.9%;L₁、L₂土壤侵蚀量分别比L₃降低65.0%、55.1%.对地表径流和淋溶损失中TN、NO₃^--N、NH₄⁺-N流失量的控制效果均为L₁＞L₂＞L₃;常规施氮(91 kg·hm^-2)水平下,L₁地表径流中TN、NO₃^--N、NH₄⁺-N流失量较L₃分别降低62.9%、45.1%、69.2%,L₂较L₃分别降低23.4%、6.9%、46.2%;杨树间作密度越大、距离林带越近,对土壤NO₃^--N、NH₄⁺-N的淋溶损失削减作用越强.同一间作密度下,随着施氮量的增加,地表径流中NO₃^--N流失比例减少,NH₄⁺-N流失比例增加;淋溶流失中
NO₃^--N、NH₄⁺-N浓度变化趋势一致,均为 N₃＞N₂＞N₁＞N₀.     

银杏叶提取物对过氧化氢刺激下的血管内皮细胞的影响

目的:探讨银杏叶提取物对血管内皮细胞的保护作用及可能的保护机制。方法:进行血管内皮细胞培养。用过氧化氢(H2O2)处理血管内皮细胞建立细胞凋亡模型。将细胞分为四组:空白对照组、H2O2处理组、单独银杏叶提取物处理组、银杏叶提取物预处理组(提前2h给药后H2O2处理)。进行MTT检测细胞的相对活力、RT-PCR检测目的基因CHOP的表达、Western Blot分析目的蛋白CHOP的表达等。结果:与对照处理组比较,H2O2处理组细胞凋亡率、CHOPmRNA相对表达及CHOP蛋白表达量明显升高。与H2O2处理组比较,银杏叶提取物预处理组细胞凋亡指数、CHOPmRNA相对表达及CHOP蛋白表达量明显降低(P0.05)。结论:作为一种清除自由基、抗氧化、抗衰老药物,银杏叶提取物可能通过调节CHOP蛋白选择性地抑制过度的内质网应激来保护血管内皮细胞。     

Potential effets of ginkgo (Ginkgo biloba,L.) on female reproduction

This minireview will briefly outline the basic knowledge concerning the provenance, biological active constituents of ginkgo (Ginkgo biloba, L.) and its general health effects. Ginkgo has been shown to affect female reproductive functions: it can affect ovarian folliculo- and oogenesis, embryogenesis, promote ovarian granulosa cell apoptosis, reduce their proliferation and the release of ovarian hormones. Usually, ginkgo extract mainly suppresses, but its constituents like amifostine, leuprorelin, quercetin and kaempherol can promote ovarian functions. This may indicate the existence of anti-reproductive ginkgo constituent(s), such as ginkgolide B and allopregnenolone which, like ginkgo extract, can promote ovarian cell apoptosis and suppress ovarian follicullogenesis and oogenesis. Ginkgo effects could be mediated by an action on brain functions, ovarian steroidogenesis, oxidative processes, intracellular regulators of ovarian cell proliferation and apoptosis and GABA receptors. Ginkgo and its molecules, ginkgolide B and allopregnenolone can be useful for prevention and treatment of reproduction-related disorders like ovarian cancer, ovarian ischemia and menopausal syndrome. On the other hand, its constituents amifostine, leuprorelin, quercetin and kaempherol could be potentially applicable as biostimulators of female reproductive processes in human and veterinary medicine and animal production. Nevertheless, application of ginkgo is still limited by insufficient or contradictory knowledge concerning its active constituents, characters, targets and mediators of its action and their functional interrelationships. Impact of ginkgo action on reproductive organs other than ovaries remains largely unknown. Addressing these issues with proper animal and clinical studies could help to understand the distinct efficacy and consequences of medical application of ginkgo.     

中药银杏制剂的心血管药理效应:机制与展望

银杏是传统的活血化瘀中药,银杏制剂是现代科技开发的植物药中最为成功的案例之一.目前研究较多的银杏制剂是银杏酮酯,其主要活性成分为银杏黄酮、银杏内酯等,具有较为广泛的心血管药理效应,对多种心血管疾病具有较好的预防和治疗效果.本文对中药银杏制剂的主要活性成分、心血管药理效应及其机制、研究展望做一述评.     

Chemical and physical properties of ginkgo (Ginkgo biloba) starch

Starch isolated from mature Ginkgo biloba seeds and commercial normal maize starches were subjected to α-amylolysis and acid hydrolysis. Ginkgo starch was more resistant to pancreatic α-amylase hydrolysis than the normal maize starch. The chain length distribution of debranched amylopectin of the starches was analyzed by using high performance anion-exchange chromatography equipped with an amyloglucosidase reactor and a pulsed amperometric detector. The chain length distribution of ginkgo amylopectin showed higher amounts of both short and long chains compared to maize starch. Naegeli dextrins of the starches prepared by extensive acid hydrolysis over 12 days demonstrated that ginkgo starch was more susceptible than normal maize to acid hydrolysis. Ginkgo dextrins also demonstrate a lower concentration of singly branched chains than maize dextrins, and unlike maize dextrin, debranched ginkgo shows no multiple branched chains. The ginkgo starch displayed a C-type X-ray diffraction pattern, compared to an A-type pattern for maize. Ginkgo starch and maize starch contained 24.0 and 17.6% absolute amylose contents, respectively.     

Adulteration of Ginkgo biloba products and a simple method to improve its detection

Extracts of ginkgo (Ginkgo biloba) leaf are widely available worldwide in herbal medicinal products, dietary supplements, botanicals and complementary medicines, and several pharmacopoeias contain monographs for ginkgo leaf, leaf extract and finished products. Being a high-value botanical commodity, ginkgo extracts may be the subject of economically motivated adulteration. We analysed eight ginkgo leaf retail products purchased in Australia and Denmark and found compelling evidence of adulteration with flavonol aglycones in three of these. The same three products also contained genistein, an isoflavone that does not occur in ginkgo leaf.Although the United States Pharmacopeia – National Formulary (USP-NF) and the British and European Pharmacopoeias stipulate a required range for flavonol glycosides in ginkgo extract, the prescribed assays quantify flavonol aglycones. This means that these pharmacopoeial methods are not capable of detecting adulteration of ginkgo extract with free flavonol aglycones.We propose a simple modification of the USP-NF method that addresses this problem: by assaying for flavonol aglycones pre and post hydrolysis the content of flavonol glycosides can be accurately estimated via a simple calculation. We also recommend a maximum limit be set for free flavonol aglycones in ginkgo extract.     

Ginkgo 11S seed storage protein family mRNA: unusual Asn-Asn linkage as post-translational cleavage site

By reducing the amount of ginkgo water-soluble polysaccharides, which occupy about 35% of the wet seed mass and interfere with the extraction of RNA, cDNA-quality mRNA was obtained from developing seeds of Ginkgo biloba. Based on the NH₂-terminal 17-amino acid sequence and an internal 12-amino acid sequence derived from the basic subunit of ginnacin, 11S-seed storage protein family of ginkgo, two degenerate oligonucleotide primers were synthesized and used for polymerase chain reaction (PCR). The resulting PCR product was used for screening the above endosperm cDNA library, and a plaque carrying the 1614 bp cDNA insert, which contained the entire coding region for a precursor of ginnacin was isolated. This is the first reported cloning of cDNA from ginkgo seeds. The deduced primary sequence is composed of a signal peptide segment (25 amino acid residues) and an acidic subunit (248 residues) followed by a basic subunit (187 residues). It was also found that the post-translational cleavage site in the ginnacin precursor is the Asn-Asn rather than the Asn-Gly bond found in a variety of the major subunit precursors in 11S seed protein family known to date. We showed that a purified soybean extract and an extract of ginkgo seeds can specifically hydrolyze-Asn²⁴⁸-Asn²⁴⁹- but not -Asn²⁴⁹-Val²⁵⁰-, in the heptapeptide Gly-Asn²⁴⁸-Asn-Val-Glu-Glu-Leu that corresponds to the ginnacin cleavage region.Abbreviations SDS-PAGE sodium dodecyl sulfate-polyacrylamide gel electrophoresis - PVDF polyvinylidene difluoride - CBB Coomassie Brilliant Blue - HPLC high-performance liquid chromatography - bp base pair(s) - PCR polymerase chain reaction     

A novel substance with allelopathic activity in Ginkgo biloba

Ginkgo (Ginkgo biloba) is one of the oldest living tree species and has been widely used in traditional medicine. Leaf extracts of ginkgo, such as the standardized extract EGb761, have become one of the best-selling herbal products. However, no bioactive compound directed at plants has been reported in this species. Therefore, we investigated possible allelopathic activity and searched for allelopathically active substances in ginkgo leaves. An aqueous methanol leaf extract inhibited the growth of roots and shoots of garden cress (Lepidium sativum), lettuce (Lactuca sativa), timothy (Phleum pratense) and ryegrass (Lolium multiflorum) seedlings. The extract was purified by several chromatographic runs and an allelopathically active substance was isolated and identified by spectral analysis to be the novel compound 2-hydroxy-6-(10-hydroxypentadec-11-enyl)benzoic acid. The compound inhibited root and shoot growth of garden cress and timothy at concentrations greater than 3 μM. The activity of the compound was 10- to 52-fold that of nonanoic acid. These results suggest that 2-hydroxy-6-(10-hydroxypentadec-11-enyl)benzoic acid may contribute to the allelopathic effect caused by ginkgo leaf extract. The compound may also have potential as a template for the development of new plant control substances.     

银杏叶多酚的机械力辅助提取及其体外抗氧化活性研究

为优化银杏叶多酚提取工艺,通过单因素试验考察填充率、球磨转速、球磨时间、乙醇浓度、料液比、提取温度、提取时间七个因素对机械力辅助提取银杏叶多酚得率的影响,以银杏叶多酚得率为响应值,采用Box-Benhnken三因素三水平响应面设计优化工艺,同时比较了4种提取方法对银杏叶多酚提取得率和抗氧化活性的差异。结果表明,机械力辅助提取银杏叶多酚的最佳工艺条件为:填充率26%、球磨转速为400rpm、球磨时间为15min。在此条件下,银杏叶多酚的得率为7.33%。机械力辅助乙醇提取银杏叶多酚得率低于碱水提取法,但是抗氧化活性高于碱水法提取的银杏叶多酚;抗氧化活性与乙醇回流法提取的银杏叶多酚相当,但是提取得率高于乙醇回流法。此提取工艺高效可行,具有一定的参考价值。     

高效液相色谱法测定银杏叶提取物中黄酮甙含量

用高效液相色谱法测定银杏叶提取物经酸水解后黄酮甙元含量．采用Ｃ１８柱,甲醇：水：磷酸（５５：４４．５：０．５）为流动相,检测波长３７０ｎｍ,方法回收率９５．１％～１０３．２％,变异系数（ＣＶ）３．１７％,１０批样品含测平均为２５．４％．     

贵州传统发酵豆制品中水解银杏黄酮苷的微生物β-葡萄糖苷酶筛选

[目的]微生物β-葡萄糖苷酶法水解银杏黄酮苷具有重要意义,不过目前这方面的研究极少。因此,本文目的是筛选到水解银杏黄酮苷的酶活高的微生物β-葡萄糖苷酶,并分析其底物选择性机制。[方法]以银杏叶提取物作为唯一碳源富集培养,从贵州传统发酵豆豉中筛选产对银杏黄酮苷水解酶活高的β-葡萄糖苷酶的菌株,并对该菌株进行鉴定。然后比较此β-葡萄糖苷酶对不同底物的选择性,同时测定此酶水解银杏黄酮苷反应的米氏常数Km及最大反应速率Vmax。最后,对不同的底物进行分子对接,分析其底物特异性机制。[结果]结果表明,筛选到的菌株GUXN01所产β-葡萄糖苷酶水解银杏黄酮苷的酶活最高,被鉴定为枯草芽孢杆菌。此β-葡糖糖苷酶对β构型的糖类以及苷类等具有广泛的底物特异性和不同的选择性,尤其对银杏黄酮苷具有很好的亲和性。分子对接研究表明枯草芽孢杆菌β-葡萄糖苷酶对银杏黄酮苷和其他糖苷类具有不同亲和性和选择性的原因主要是酶结构和底物分子结构的相互作用力的差异导致的。[结论]这些发现为GUXN01所产的β-葡萄糖苷酶应用于水解银杏黄酮苷类生产相应苷元奠定了良好的基础。