ライフサイエンスコーパス: Methanosarcina acetivorans

1 rized a member of the YrbG family, MaX1 from Methanosarcina acetivorans.

2 mp loader (RFC) from the mesophilic archaeon Methanosarcina acetivorans.

3 e family from the methane-producing archaeon Methanosarcina acetivorans.

4 d in Escherichia coli expressing pylBCD from Methanosarcina acetivorans.

5 methyltransferase MtmB1, was introduced into Methanosarcina acetivorans.

6 a new form of clamp loader from the archaeon Methanosarcina acetivorans.

7 MaPgb from the strictly anaerobic methanogen Methanosarcina acetivorans.

8 ogs, RPA1, RPA2, and RPA3, from the archaeon Methanosarcina acetivorans.

9 on the naturally occurring plasmid pC2A from Methanosarcina acetivorans.

10 Methanosarcina acetivorans, a strictly anaerobic methane

11 old/one zinc finger replication protein A in Methanosarcina acetivorans and Methanopyrus kandleri exh

12 ence of Methanosarcina barkeri with those of Methanosarcina acetivorans and Methanosarcina mazei.

13 nococcus jannaschii, Archaeoglobus fulgidus, Methanosarcina acetivorans, and Methanosarcina barkeri p

14 chaeoglobus fulgidus, Methanopyrus kandleri, Methanosarcina acetivorans, and Methanosarcina mazei.

15 e isozymes of methanol methyltransferases in Methanosarcina acetivorans C2A and are among the most hi

16 The mtaA1, mtaA2, and mtbA genes of Methanosarcina acetivorans C2A encode putative methanol-

17 Methanosarcina acetivorans C2A encodes three putative hy

18 Methanosarcina acetivorans C2A is able to convert severa

19 clones were isolated after transformation of Methanosarcina acetivorans C2A with the mutagenized plas

20 en in this process, we tested the ability of Methanosarcina acetivorans C2A, a metabolically versatil

21 oson mutagenesis of a methanogenic archaeon, Methanosarcina acetivorans C2A, which because of its ind

22 The corresponding mutation in Methanosarcina acetivorans C2A, which cannot grow on H(2

23 s and characterized the encoded enzymes from Methanosarcina acetivorans C2A.

24 sequence of an acetate-utilizing methanogen, Methanosarcina acetivorans C2A.

25 ere the first use of directed mutagenesis in Methanosarcina acetivorans C2A.

26 lyses to study the structure/function of the Methanosarcina acetivorans clamp loader or replication f

27 rolysine, a 761 base-pair genomic segment in Methanosarcina acetivorans containing the pylT gene (enc

28 ed a markerless tRNA(Pyl) deletion strain of Methanosarcina acetivorans (DeltapylT) that cannot decod

29 bacterial Cas9 protein for genome editing in Methanosarcina acetivorans, enabling efficient gene dele

30 The genome of Methanosarcina acetivorans encodes three homologs, initi

31 Interestingly, the euryarchaeon Methanosarcina acetivorans harbors multiple functional R

32 Unlike most organisms, Methanosarcina acetivorans harbors multiple functional R

33 The Methanosarcina acetivorans hdrED1 operon is constitutive

34 on of the slow-growing methanogenic archaeon Methanosarcina acetivorans Introduction of both insertio

35 ation of McrA from the methanogenic archaeon Methanosarcina acetivorans lacking tfuA and/or ycaO reve

36 t comparison of histones from M. jannaschii, Methanosarcina acetivorans (largest Archaeal genome, 5.8

37 se 1 operons (mtaCB1, mtaCB2, and mtaCB3) in Methanosarcina acetivorans led to the suggestion that ea

38 ere identified in M. jannaschii (Mj0601) and Methanosarcina acetivorans (Ma2851), and recombinant Ma2

39 TLPs from Bacillus thuringiensis (BtTLP) and Methanosarcina acetivorans (MaTLP) display biochemical p

40 n methanol-grown cells of the marine isolate Methanosarcina acetivorans metabolically labeled with 14

41 The regulation of the Methanosarcina acetivorans mtsD, mtsF and mtsH genes, wh

42 naturally "truncated" homologs of NifB from Methanosarcina acetivorans (NifB(Ma)) and Methanobacteri

43 standing of this family, a flavoredoxin from Methanosarcina acetivorans of the Archaea domain was pro

44 Here we show that Methanosarcina acetivorans possesses three operons encod

45 Methanosarcina acetivorans produces acetate, formate, an

46 , 3046 unique peptides covering 566 distinct Methanosarcina acetivorans proteins were identified from

47 tandem polypeptide repeats that comprise the Methanosarcina acetivorans S-layer protein and propose a

48 haea and that the polymerase from mesophilic Methanosarcina acetivorans shows identical behaviour.

49 Methanosarcina acetivorans strain C2A is a marine methan

50 Methanosarcina acetivorans strains bearing deletions of

51 ein the purification and characterization of Methanosarcina acetivorans subunit D in complex with sub

52 MacDinB-1, the homolog from the euryarchaeon Methanosarcina acetivorans that is characterized in this

53 The Methanosarcina acetivorans Thg1 (MaThg1) gene contains a

54 otein overproduction system was developed in Methanosarcina acetivorans to facilitate biochemical cha

55 Here, we study the methanogenic archaeon Methanosarcina acetivorans using assays of ATP hydrolysi

56 Gene-deletion and growth experiments in Methanosarcina acetivorans, using sulfide as the sole su

57 ltisubunit sodium/proton antiporter (Mrp) of Methanosarcina acetivorans was investigated with a mutan

58 rotein MA4561 from the methanogenic archaeon Methanosarcina acetivorans was originally predicted to b

59 a representative of this new group of RPA in Methanosarcina acetivorans, we made two deletion mutants

60 ologs (TBP1, TBP2, and TBP3) in the archaeon Methanosarcina acetivorans were investigated by using ge

61 termed Hsp60-4 and Hsp60-5, in the archaeon Methanosarcina acetivorans, which also has Hsp60-1, Hsp6