首页> 外文期刊>Applied and Environmental Microbiology >Stenoxybacter acetivorans gen. nov., sp. nov., an Acetate-Oxidizing Obligate Microaerophile among Diverse O2-Consuming Bacteria from Termite Guts
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Stenoxybacter acetivorans gen. nov., sp. nov., an Acetate-Oxidizing Obligate Microaerophile among Diverse O2-Consuming Bacteria from Termite Guts

机译:乙炔乙酸杆菌属。十一月,sp。 nov。,来自白蚁肠道的各种O2食用细菌中的乙酸氧化专性微嗜氧菌

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In termite hindguts, fermentative production of acetate—a major carbon and energy source for the insect—depends on efficient removal of inwardly diffusing oxygen by microbes residing on and near the hindgut wall. However, little is known about the identity of these organisms or about the substrate(s) used to support their respiratory activity. A cultivation-based approach was used to isolate O2-consuming organisms from hindguts of Reticulitermes flavipes. A consistently greater (albeit not statistically significant) number of colonies developed under hypoxia (2% [vol/vol] O2) than under air, and the increase coincided with the appearance of morphologically distinct colonies of a novel, rod-shaped, obligately microaerophilic β-proteobacterium that was Eikenella corrodens). Nearly identical organisms (and/or their 16S rRNA genes) were obtained from geographically separated and genetically distinct populations of Reticulitermes. PCR-based procedures implied that the novel isolates were autochthonous to the hindgut of R. flavipes and comprised ca. 2 to 7% of the hindgut prokaryote community. Representative strain TAM-DN1 utilized acetate and a limited range of other organic and amino acids as energy sources and possessed catalase and superoxide dismutase. On solid medium, the optimal O2 concentration for growth was about 2%, and no growth occurred with O2 concentrations above 4% or under anoxia. However, cells in liquid medium could grow with higher O2 concentrations (up to 16%), but only after proportionately extended lag phases. The genetic and physiological distinctiveness of TAM-DN1 and related strains supports their recognition as a new genus and species, for which the name Stenoxybacter acetivorans gen. nov., sp. nov. is proposed.
机译:在白蚁后肠中,醋酸盐的发酵生产是昆虫的主要碳和能源,它依赖于后肠壁上和附近微生物的有效去除向内扩散的氧气。然而,关于这些生物的身份或用于支持其呼吸活动的基质的了解甚少。一种基于培养的方法被用来从网状白蚁的后肠中分离出消耗氧气的生物。在缺氧条件下(2%(vol / vol)O2)形成的菌落数量始终比在空气中更大(尽管在统计学上不显着),并且这种增加与新型杆状专心的形态不同的菌落的出现相吻合微小的需氧性β-变形杆菌,即腐蚀的艾肯氏菌)。从网状白蚁的地理上分离和遗传上不同的种群中获得了几乎相同的生物(和/或它们的16S rRNA基因)。基于PCR的程序暗示该新分离株是黄褐肉座菌的后肠的自体,并且包含约3个。后肠原核生物群落的2%至7%。代表性菌株TAM-DN1利用乙酸盐和有限范围的其他有机和氨基酸作为能源,并具有过氧化氢酶和超氧化物歧化酶。在固体培养基上,用于生长的最佳O2浓度约为2%,而当O2浓度高于4%或处于缺氧状态时,则没有生长发生。但是,液体培养基中的细胞可以以更高的O2浓度(高达16%)生长,但只能在成比例延长的滞后阶段之后才能生长。 TAM-DN1和相关菌株的遗传和生理独特性支持它们被识别为一种新的属和种,其名称为醋酸乙缩杆菌。十一月,sp。十一月被提议。

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