四川南江两种水青冈种群遗传多样性初步研究

利用凝胶电泳法研究米心水青冈（Ｆａｇｕｓｅｎｇｌｅｒｉａｎａ）和巴山水青冈（Ｆ．ｐａｓｈａｎｉｃａ）２个种４个种群的遗传多样性。所测定的酶系统包括：过氧化物酶（ＰＸ１和ＰＸ２）,磷酸葡萄糖脱氢酶（ＰＧＤ）,酸性磷酸化酶（ＡＣＰ）,超氧物歧化酶（ＳＯＤ）,谷氨酸草酰乙酸转氨酶（ＧＯＴ１和ＧＯＴ２）,异柠檬酸脱氢酶（ＩＤＨ）,磷酸果糖异构酶（ＰＧＩ）,甲基萘醌还原酶（ＭＮＲ）,葡萄糖磷酸变位酶（ＰＧＭ１和ＰＧＭ２）和苹果酸脱氢酶（ＭＤＨ２）１０种酶系统。测定和分析了水青冈等位基因频率、遗传多样性、固定指数、Ｈａｒｄｙ－Ｗｅｉｎｂｅｒｇ平衡和遗传距离指标,为进一步研究水青冈属各种间的亲缘关系和进化提供了科学依据     

亮叶水青冈（Fagus lucida）种群遗传多样性初步研究

本文利用凝胶电泳法研究亮叶水青冈（Ｆａｇｕｓｌｕｃｉｄａ）种内遗传多样性。所测定的酶系统包括：过氧化物酶（ＰＸ１和ＰＸ２）、磷酸葡萄糖脱氢酶（ＰＧＤ）、谷氨酸草酰乙酸转氨酶（ＧＯＴ１和ＧＯＴ２）、异柠檬酸脱氢酶（ＩＤＨ）、甲基荼醌还原酶（ＭＮＲ）、葡萄糖磷酸变位酶（ＰＧＭ１和ＰＧＭ２）,苹果酸脱氨酶（ＭＤＨ２）、酸性磷酸酶（ＡＣＰ）和磷酸果糖升构酶（ＰＧＩ）９种酶系统１１个基因位点。测定和分析了亮叶水青冈２地理种群的等位基因频率,固定指致,基因多祥性和遗传距离,为进一步研究水青冈的遗传变异和种内种间关系提供了科学依据。     

基于ITS和ndhF-rpl32序列的荞麦种间亲缘关系分析

荞麦起源于我国, 演化形成了丰富的物种和遗传多样性。为了有效研究和利用荞麦及其野生种资源, 以从四川、甘肃、贵州等地采集的荞麦属(Fagopyrum)10个种(含变种、亚种和复合体种)共71份材料为对象, 通过ITS和叶绿体ndhF-rpl32序列分析, 利用MEGA5.0构建系统进化树, 探讨了荞麦种内及种间亲缘关系。结果表明, 在ITS序列矩阵中, 序列长度为725 bp, 信息位点为150个, 占序列总长度的20.7%; 在ndhF-rpl32序列矩阵中, 序列长度为940 bp, 信息位点为158个, 占序列总长度的16.8%。由ITS序列和ndhF-rpl32序列构建的两个进化树都可以将71份材料分为大粒荞麦种组和小粒荞麦种组; 其中, 大粒荞麦种组包括栽培苦荞和米苦荞(F. tataricum)、金荞复合体(F. cymosum complex)、栽培甜荞(F. esculentum)和野生甜荞(F. esculentum ssp. ancestralis); 小粒荞麦种组包括齿翅野荞(F. gracilipes var. odontopterum)、疏穗小野荞(F. leptopodum var. grossii)、小野荞(F. leptopodum)、密毛野荞(F. densovillosum)、细柄野荞(F. gracilipes)和硬枝万年荞(F. urophyllum)。而ndhF-rpl32序列构建的系统发育树还能区分栽培甜荞和野生甜荞, 具有更好的聚类效果。另外, 与栽培甜荞相比, 金荞复合体与栽培苦荞的亲缘关系更近。该研究为荞麦属种的分类和条形码研究提供了一定的科学依据。     

基于3种线粒体标记探讨中日沿海角木叶鲽遗传多样性差异

角木叶鲽(Pleuronichthys cornutus)是东亚沿海重要的鲽形目经济鱼类, 为更好地保护和开发利用其种质资源, 有必要全面了解其遗传背景。本研究测定了中国和日本沿海7个群体200尾角木叶鲽线粒体控制区(CR) 5'端、细胞色素b (Cytb)和NADH脱氢酶第二亚基(ND2)基因序列, 比较不同标记在解析遗传多样性和种群结构上的可行性与有效性, 阐明中日沿海角木叶鲽群体间出现遗传分化的分子机制。CR序列分析发现中日沿海7个角木叶鲽群体遗传多样性表现出较高的单倍型多样性(H_d = 0.9699)和较低的核苷酸多样性(π = 0.0061); 各群体间无显著的遗传分化(F_ST = -0.0197-0.0184, P > 0.05); 单倍型网络未显示出明显的地理聚群和谱系结构; 分子方差分析(AMOVA)表明变异主要发生在群体内部(> 99.17%)。进一步通过Cytb和ND2基因分别与CR序列对比分析, 结果表明群体遗传多样性均表现为高H_d (0.9683-0.9829)低π (0.0050-0.0063)模式, 仅有ND2基因分析F_ST值(F_ST = 0.0302, P < 0.05)显示了中国碣石(GDJS)和日本明石(JAP)群体间显著的低水平遗传分化现象。CR、Cytb和ND2的单倍型网络图均无明显的地理聚类和谱系结构, AMOVA分析也显示变异主要来源于群体内(> 98.39%)。种群历史动态分析结果显示, 角木叶鲽可能在第四纪中更新世晚期经历了群体扩张事件, 扩张时间分别为31.93-9.58万年前(CR)、27.53-22.02万年前(Cytb)和26.99-18.75万年前(ND2)。综上所述, 中日沿海的角木叶鲽具有较高遗传多样性, GDJS和JAP群体间存在低度分化; ND2基因比CR和Cytb序列更适于分析角木叶鲽种群遗传结构, 选择多个遗传标记可有效弥补单一标记分析遗传多样性的局限性; 推测冰期两大独立避难所的形成及GDJS和JAP群体距离相隔较远是其发生遗传分化的主要原因。研究结果为中日沿海角木叶鲽渔业资源的种质保护与可持续利用提供了理论依据。     

不同光脉冲方案对光下最大荧光参数及其计算参数的影响

光下最大荧光(F_m′)是植物生理生态研究中的重要参数,一般采用饱和脉冲(RF)方案来估计.然而,光系统Ⅱ(PSⅡ)受体库的反馈调节会影响RF方案对F_m′估计的准确性.为消除PSⅡ受体库反馈调节的影响,根据光脉冲强度(Q′)与叶绿素荧光(F′)的线性关系提出多相脉冲(MPF)方案,估算Q′无穷大时的F′(即F_m′).本研究采用MPF和RF方案分别对苦槠、青冈和乌桕3个树种叶片的叶绿素荧光和气体交换数据进行同步测量,并对两种方案估计的F_m′及其计算参数PSⅡ光化学效率(Φ_PSII)、PSⅡ的电子传递速率(J)、最大电子传递速率(J_max)、叶肉导度(g_m)和叶绿体内CO₂浓度(C_c)等光合参数进行比较,分析两种方案对3个树种叶片6个光合参数的影响.结果表明: 当光合有效辐射(PAR)<200 μmol·m^-2·s^-1时,两种方案对苦槠、青冈和乌桕叶片F_m′、Φ_PSII和J的估计无显著影响;当PAR>200 μmol·m^-2·s^-1时,采用MPF方案获得的苦槠、青冈和乌桕的F_m′分别比RF方案获得的F_m′高3.5%～5.2%、11.7%～18.0%和3.2%～7.1%;当PAR>200 μmol·m^-2·s^-1时,采用MPF方案获得的Φ_PSII、J和J_max分别不同程度地大于RF方案获得的参数,g_m和C_c分别不同程度地小于RF方案获得的参数.说明当PAR较低(<200μmol·m^-2·s^-1)时,MPF与RF方案对植物叶片F_m′、Φ_PSII、J的估计没有显著影响;当PAR较高(≥200μmol·m^-2·s^-1)时,MPF与RF方案对植物叶片F_m′、Φ_PSII、J、J_max、g_m和C_c的估计有显著影响,且RF方案对植物叶片的F_m′、Φ_PSII、J和J_max比MPF方案分别有不同程度的低估,对g_m和C_c则有不同程度的高估.     

条形柄锈菌小麦专化型葡萄糖-6-磷酸脱氢酶基因PsG6PDH1的表达特征及功能分析

葡萄糖-6-磷酸脱氢酶是磷酸戊糖途径中的关键限速酶。基于已测序的条形柄锈菌小麦专化型基因组序列,利用RT-PCR方法克隆了该病菌葡萄糖-6-磷酸脱氢酶PsG6PDH1的全长cDNA序列（1 497bp）,编码498个氨基酸的蛋白。编码蛋白含有葡萄糖-6-磷酸脱氢酶的保守功能域。系统进化分析发现,PsG6PDH1与禾柄锈菌小麦专化型的G6PDH聚为一簇。qRT-PCR分析表明,PsG6PDH1在病菌侵染早期的表达明显上调,其中侵染24h时表达量最高,为对照夏孢子的30倍。将PsG6PDH1导入酿酒酵母G6PDH缺失突变体中成功表达,并表现出较强的葡萄糖-6-磷酸脱氢酶活性,明显酵母增强了菌株对过氧化氢的耐受性。由此推测,PsG6PDH1可能参与了条形柄锈菌小麦专化型在侵染寄主时抵御寄主的氧化胁迫反应。研究结果为进一步研究该病菌基础代谢及侵染机理奠定一定的理论基础。     

广西区西南桦天然居群遗传多样性的研究

 以采自广西区11个西南桦(Betula alnoides)天然居群的种子培育出的幼苗为材料,取其嫩叶开展21种酶系统的水平切片淀粉凝胶电泳实验,运用作者改进的Tris-马来酸提取缓冲液 (含30%PVP 40 000和1%2-巯基乙醇),筛选出AMP(氨基肽酶Aminopeptidase)、FBA(果糖二磷酸酶Fructose-bisphosphate aldolase)、GDH(谷氨酸脱氢酶Glutamate dehydrogenase)、G6PD(6-磷酸葡萄糖脱氢酶Glucose-6-phosphate dehydrogenase)、IDH(异柠檬酸脱氢酶Isocitrate dehydrogenase)、MDH(苹果酸脱氢酶Malate dehydrogenase)、PGD(6-磷酸葡萄糖酸脱氢酶Phosphogluconate dehydrogenase)、PGI(磷酸葡萄糖异构酶Phosphoglucoisomerase)、PGM(磷酸葡萄糖变位酶Phosphoglucomutase)和SKD(莽草酸脱氢酶Shikimate dehydrogenase)等10种酶,获得了清晰且可重复的酶谱。通过谱带遗传分析确定了15个位点,其中有6个单态位点,9个多态位点 (0.95标准),具40个等位基因。在居群水平上,西南桦的多态位点百分数 (P) 为55.2%,平均每个位点的等位基因数 (A) 为2.00,平均预期杂合度 (He) 为0.204。均超过Hamrick (1992)等提出的远交风媒木本植物的平均值(53.0%,184%和0154),表明西南桦的遗传变异水平高。在11个西南桦居群内,实际杂合度 (Ho)均高于预期杂合度,出现杂合子过量,可能存在利于杂合子的自然选择。西南桦遗传多样性与地理位置相关不显著。居群2 (靖西地州)、5 (平果海城)、9 (田林者苗) 包含绝大部分的等位基因,而且具较高的遗传多样性,应加以保护和管理,作为其基因资源就地保存的基地。本研究解决了以西南桦嫩叶为材料进行等位酶分析的关键技术,为进一步开展西南桦乃至桦木属树种的遗传结构和遗传多样性等提供了技术基础;同时掌握了西南桦天然居群的遗传多样性现状,为其有效保护和合理经营以及西南桦的遗传改良提供了理论依据。     

肺炎克雷伯菌blaCARB-2基因的分布及结构分析

为探讨β-内酰胺酶基因在临床分离肺炎克雷伯菌的分布及其相关可移动遗传元件的结构,本文利用基因组测序、PCR、分子克隆、接合转移和基因组学分析等方法,在对240株临床分离的肺炎克雷伯菌进行混合基因组测序的基础上,着重研究了bla_CARB-2等耐药性基因相关可移动遗传元件的结构及其在肺炎克雷伯菌基因组的定位,克隆获得耐药性质粒携带的若干耐药性基因并测定了它们的功能。结果显示,在240株肺炎克雷伯菌中检出11种β-内酰胺酶基因,其中1株肺炎克雷伯菌(KP1276)被检出bla_CARB-2基因,阳性率为0.42% (1/240);bla_CARB-2位于一个大小为182,450 bp的可接合转移质粒(pKP1276-182),pKP1276-182共编码222个基因,包含7个耐药性基因,分别是bla_CARB-2、bla_KLUC、aadA1、aadA2、cmlA1、dfrA1和sul2。bla_CARB-2是首次在肺炎克雷伯菌中被检出,且bla_CARB-2与其他3个耐药性基因一起构成一个新型结构的1型整合子(int-bla_CARB-2-aadA2-cmlA1-aadA1);对其中的3个耐药性基因bla_CARB-2、aadA2和CmlA1进行了分子克隆和耐药性测定,结果显示它们对相应药物都具有一定的耐药性, 其中bla_CARB-2对青霉素类β-内酰胺药物具有较高的耐药性。本研究结果表明,bla_CARB-2基因已经在肺炎克雷伯菌中出现,其由1型整合子携带编码位于一个可接合转移的质粒上,bla_CARB-2基因有可能在相同及不同种属肠杆菌之间进行水平转移,引起耐药性播散。     

三平正并殖吸虫发育过程中的同工酶谱

采用同工酶电泳技术对三平正并殖吸虫童虫、早期成虫和后期成虫的葡萄糖磷酸变位酶、葡萄糖磷酸异构酶和葡萄糖－６－磷酸脱氢酶的同工酶进行了研究,结果显示三平正并殖吸虫由童虫向成熟期发育过程中,葡萄糖磷酸变位酶和葡萄糖磷酸异构酶的同工酶谱趋于复杂,酶带数目后期成虫〉早期成虫〉童虫;而葡萄糖－６－磷酸脱氢酶同工酶谱则趋于简单,童虫或未成熟虫体酶带数目较成熟虫体为多。三种酶系统的同工酶排列型式显示,吸虫由童虫     

罗汉松科3种植物茎和根木质部水分运输、解剖结构与机械强度之间的关系

水力失效是植物干旱死亡的主要机制。量化分析水力性状的种间和器官间差异是预测树木在气候变化下的响应甚至生存能力的基础。该研究对比分析了罗汉松科3种植物器官(茎和根)水平上水力功能性状的差异, 并探讨其与解剖结构和机械强度之间的关系。在湿生同质园内选择罗汉松科3种植物, 测定了茎和根木质部水力功能性状(最大比导率(K_s)和栓塞抗性(P₅₀))、解剖结构性状(管胞直径(D_t)、水力直径(D_h)、管胞密度(N_t)、管胞壁厚(T_w)、纹孔膜直径(D_p)和纹孔密度(N_p))和机械强度(木材密度(WD)和管胞厚度跨度比((t/b)²))。结果发现: (1)罗汉松科3种植物茎木质部不存在效率-安全权衡, 而根木质部存在权衡。(2)茎K_s与D_p显著正相关, 与(t/b)²和WD无关; 茎P₅₀与D_p极显著负相关, 与(t/b)²和WD无关。(3)根K_s与D_h显著正相关, 与T_w和(t/b)²极显著负相关; 根P₅₀与T_w、(t/b)²和WD均极显著正相关。在罗汉松科植物中, 根木质部性状与输水效率和栓塞抗性的密切关系是解释其存在效率-安全权衡的基础, 而茎木质部的过度建造是茎不存在效率-安全权衡的原因, 木质部的过度建造仍需要更多的实验证据。     

Relations between heterosis and enzymatic polymorphism in populations of cultivated sunflowers (Helianthus annuus L.)

Nine polymorphic isoenzymatic systems were studied in 39 cultivated sunflower populations originating from ten countries. Analysis of combining abilities with four tester lines was also performed on these populations for seed yield, seed moisture and seed oil content. The MDH, PGI, PGD and GOT systems appeared to provide the best discrimination of specific combining ability effects with the four testers. The MDH and GOT systems provided a between-population structure that was consistent with the country of origin.Abbreviations MDH Malate dehydrogenase - PGD phosphogluconate dehydrogenase - PGI phosphoglucoisomerase - PGM phosphoglucomutase - ACO aconitase hydratase - ADH2 alcohol dehydrogenase - GOT glutamate oxaloacetate transaminase - LAP leucine amino peptidase - EST esterases     

Inheritance and linkage relationships of ten isozyme genes in hazelnut

Summary The inheritance of 6-phosphogluconate dehydrogenase (6PGD), malate dehydrogenase (MHD), aconitase (ACO), phosphoglucomutase (PGM), phosphoglucoisomerase (PGI), and glutamate-oxalacetate transaminase (GOT) polymorphic isozymes was studied in leaf extracts of nine hazelnut progenies using horizontal starch gel electrophoresis. Evidence of Mendelian inheritance was obtained for ten loci: 6-Pgd-2, Mdh-1, Aco-1, Aco-2, Pgm-1, Pgm-2, Pgm-3, Pgi-2, Pgi-3, and Got-2, which permitted the analysis of 28 alleles (2.8 per locus). The presence of null alleles was detected in Pgm-1 and Pgm-3. Joint segregation analysis of pairs of isozymes revealed four linkages: Mdh-1-Pgi-2, Aco-2-Pgm-2, Pgm-1-Pgm-3, and 6Pdg-2-Pgm-2.     

The relationship between red cell aging and enzyme activities in experimental animals.

1. The relationship between red cell aging and enzyme activities was studied in rabbit, guinea-pig, hamster, rats (F344/N and SD), and mice (BALB/c and DBA/2). 2. The activities of six enzymes: glucose-6-phosphate dehydrogenase (G-6-PD), 6-phosphogluconate dehydrogenase (6-PGD), hexokinase (Hx), glutamate oxaloacetate transminase (GOT), lactate dehydrogenase (LDH) and acetylcholinesterase (AChE), were measured in the red cells of different ages which were obtained either by centrifugation or experimental anaemia. 3. Hx, AChE and GOT activities were much higher in younger red cells than in older cells, hence the activities of these enzymes may be used as an indicator of age of the cells.     

棉铃虫地理种群的等位酶变异

利用聚丙烯酰胺梯度凝胶电泳检测了棉铃虫Helicoverpa armigera的13种等位酶：α-磷酸甘油脱氢酶(α-GPDH)、酸性磷酸酯酶(ACPH)、碱性磷酸酯酶(ALP)、醛氧化酶(AO)、酯酶(EST)、谷氨酸草酰乙酸转氨酶(GOT)、己糖激酶(HEX)、亮氨酸氨肽酶(LAP)、乳酸脱氢酶(LDH)、苹果酸脱氢酶(MDH)、苹果酸酶(ME)、磷酸葡萄糖变位酶(PGM)和黄嘌呤脱氢酶(XDH),染色采用双染法。对其中9种等位酶的遗传变异进行了分析,包括13个位点,6个位点表现出多态性,7个位点是单态的,其中多态性位点比例为46.15%。AO、GOT、LAP、LDH、ME和XDH计算出棉铃虫的平均杂合度为0.1160,南京、成都、武穴、衡阳和哈密5个种群的平均遗传距离为0.0008～0.0293,平均遗传相似度为0.9707～0.992。棉铃虫种群内存在很高的遗传多态性,而已测定的种群间遗传分化程度较小,种群间没有基因交流的障碍。迁飞阻碍了不同地理种群间的遗传分化。     

Complex chromosome homologies between the rhesus monkey (Macaca mulatta) and man

The chromosome localization and gene synteny of soluble malate dehydrogenase (MDH1), soluble isocitrate dehydrogenase (IDH1), mitochondrial superoxide dismutase (SOD2), phosphoglucomutase-3 (PGM3), mitochondrial malate dehydrogenase (MDH2), beta-glucuronidase (GUSB), nucleoside phosphorylase (NP), pyruvate kinase M2 (PKM2), hexosaminidase A (HEXA), inosine triphosphatase (ITPA), and N-acetyl-alpha-D-galactosaminidase (NAGA) were determined in the rhesus monkey using somatic cell hybrids. Comparison with the human and Pongidae syntenic groups shows that chromosome banding homologies do not always correlate with gene mapping data.     

Genetic structure of the populations of native inhabitants in the northeastern USSR. V. The Chukot Evens

The genetic structure of two Chukot Evens subpopulations (314 individuals) for electrophoretic protein systems and taste sensitivity to PTC was studied. 17 of the 39 loci were polymorphic (43.59%). The following systems were completely monomorphic: diaphorase NAD H (Dia); glucose-6-phosphate dehydrogenase (G-6-PD); glutamatoxalate transaminase (GOT); carbonic anhydrase (Ca-1); catalase (Ct), lactate dehydrogenase (loci LDH-A and LDH-B); leucine aminopeptidase (Lap); malate dehydrogenase (MDH); purine nucleoside phosphorylase (PNP); superoxide phosphorylase (PNP); superoxide dismutase (SOD); phosphoglucomutase-2 (PGM2); cholinesterase (locus E1); red cell esterase (4 loci); albumin (Alb); hemoglobin (Hb A and B); ceruloplasmin (Cp); and blood, gren, using the standard method. The following systems were polymorphic: red cell acid phosphatase (AcP); phosphoglucomutase-1 (PGM1); 6-phosphogluconate dehydrogenase (PGD); glutamatepyruvate transaminase (GPT); glyoxalase-1 (GLO-1); esterase (EsD); adenilatkinase (AK); alkaline phosphatase (Pp); cholinesterase (locus E2); haptoglobin (Hp); transferrin (Tf); group-specific component (Gc) and ABO, MN, Lewis, P blood groups and taste sensitivity to PTC. The following allele frequencies for polymorphic loci have been detected: AKI = 0.994; GLO = 1I = 0.082; GPT1 = 0.653; AcPA = 0.400; AcPB = 0.599; AcPC = 0.001; PGDA = 0.944; PGM1(1) = 0.906; EsD1 = 0.897; E2+ = 0.048; HpI = 0.394; GcI = 0,919; Tfc = 0.987; r(O) = 0.669; p(A) = 0.184; q(B) = 0.146; M = 0.711; Le = 0.411; P1+ = 0.521; t = 0.295. The genetic structure of Chukot Evens population is significantly nearer to that of the other ethnic groups of the North-East, in comparison with the genetic structure of Evenks of the Middle Siberia.     

Subtyping of phosphoglucomutase locus 1 (PGM1) polymorphism in some populations of Rwanda: description of variant phenotypes, "haplotype" frequencies,and linkage disequilibrium data.

Some populations of Rwanda (South Twa Pygmies, Hutu, and Tutsi) have been analyzed by acid starch gel electrophoresis for the subtyping of PGM1 polymorphism. The new polymorphic third PGM11 allele, the PGM1(1Twa), which we recently detected in Twa Pygmies from North Rwanda, has not been found in this survey, whereas the rare PGM1(6) allele attains subpolymorphic frequencies in all groups. Comparison between the various populations of Rwanda shows that they differ significantly from each other with the exception of South Twa Pygmies and Tutsi. A relatively low frequency (9.6%) of the PGM1(2S) allele appears to be typical of North Twa Pygmies; a low frequency of PGM1(2F) (1.2%-3.6%) has been found in all these groups but not in the Hutu (6.4%); and a particularly high incidence of the PGM1(1F) allele (the highest so far reported) has been observed in the South Twa Pygmies (20%) and in the Tutsi (18%). The PGM1(1Twa) and PGM1(6) enzymes, which in acid starch gel are not distinguishable, can be clearly differentiated by isoelectric focusing. In addition, the same technique has shown that the rare PGM1(7) allele observed in one Hutu is different from that found at polymorphic frequency in the Japanese and from a rare PGM1(7) allele found in Germany. On the very likely hypothesis that the PGM1(1S), PGM1(1F), PGM1(2S), and PGM1(2F) result from variations at two different polymorphic sites, 1/2 and F/S, within the PGM1 structural gene, all the available population data have been analyzed to investigate whether preferential combinations (haplotypes) were identifiable. Whereas Caucasians show a prevalence of 2F and 1S combination with an 8.02% mean value of linkage disequilibrium expressed as % Dmax, from the very few and scattered African data, it is impossible to draw any inference at present.     

Red-cell enzyme polymorphisms in the Reggio Calabria province (Italy)

Acid phosphatase (ACP1), adenosine deaminase (ADA), esterase D (ESD), glyoxalase 1 (GLO1), phosphogluconate dehydrogenase (PGD) and phosphoglucomutase 1 and 2 (PGM1 and PGM2) polymorphisms have been studied in the Reggio Calabria province (Southern Italy). The ACP1*A allele and ADA, GLO1, PGD and PGM1 systems have frequencies similar to those reported for Sicily and Southern Italy.