Füglistaller P, Suter F, Zuber H
Biol Chem Hoppe Seyler. 1985 Oct;366(10):993-1001. doi: 10.1515/bchm3.1985.366.2.993.
Three linker polypeptides of the phycobilisome from the cyanobacterium Mastigocladus laminosus were isolated: A 8.9-kDa polypeptide, L8.9R(C), which is probably associated with C-phycocyanin, a 34.5-kDa polypeptide, L34.5,PCR, which forms a complex with C-phycocyanin, and a 34.5-kDa polypeptide, L34.5,PECR, which is linked to phycoerythrocyanin. The complete amino-acid sequence (80 residues) of the L8.9R(C) polypeptide was determined as well as the N-terminal 44 residues of both L34.5R polypeptides and the 114 C-terminal residues of L34.5,PECR. L8.9R(C) is homologous to L8.9C (Füglistaller et al. (1984) Hoppe-Seyler's Z. Physiol. Chem. 365, 1085-1096) and to the C-terminal sequence of L34.5,PECR. The N-terminal sequences of L34.5,PECR and L34.5,PCR exhibit 34% homology. The 44 N-terminal residues of L34.5,PECR are related to the beta-subunit of phycoerythrocyanin (23% homology), while the C-terminal sequence of L34.5,PECR is more related to alpha PEC (21% homology within 60 residues). This suggests that the 30-kDa-linker polypeptide family originates from a fusion of the alpha- and beta-subunit genes and the corresponding intercistronic DNA sequence, as might have arisen through mutation in the stop-codon of the beta-subunit gene. Hence, all polypeptides of the phycobilisome (including perhaps the anchor polypeptide) may be derived from an early ancestor phycobiliprotein subunit, which itself is also related to myoglobin (Schirmer et al. (1985) J. Mol. Biol. 184, 251-277).
一种8.9 kDa的多肽,L8.9R(C),可能与C-藻蓝蛋白相关;一种34.5 kDa的多肽,L34.5,PCR,它与C-藻蓝蛋白形成复合物;还有一种34.5 kDa的多肽,L34.5,PECR,它与藻红胆素蛋白相连。测定了L8.9R(C)多肽的完整氨基酸序列(80个残基)以及两种L34.5R多肽的N端44个残基和L34.5,PECR的114个C端残基。L8.9R(C)与L8.9C(Füglistaller等人,(1984)《霍普-赛勒生理化学杂志》365卷,1085 - 1096页)以及L34.5,PECR的C端序列同源。L34.5,PECR和L34.5,PCR的N端序列具有34%的同源性。L34.5,PECR的44个N端残基与藻红胆素蛋白的β亚基相关(同源性为23%),而L34.5,PECR的C端序列与α-PECR更相关(在60个残基内同源性为21%)。这表明30 kDa连接多肽家族起源于α亚基和β亚基基因以及相应的基因间DNA序列的融合,这可能是由于β亚基基因终止密码子的突变而产生的。因此,藻胆体的所有多肽(可能包括锚定多肽)可能都源自一个早期的祖先藻胆蛋白亚基,该亚基本身也与肌红蛋白相关(Schirmer等人,(1985)《分子生物学杂志》184卷,251 - 277页)。